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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT04641013
Registration number
NCT04641013
Ethics application status
Date submitted
12/11/2020
Date registered
23/11/2020
Titles & IDs
Public title
Age-related Clonal Haematopoiesis in an HIV Evaluation Cohort (ARCHIVE)
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Scientific title
Age-related Clonal Haematopoiesis in an HIV Evaluation Cohort (ARCHIVE): a follow-on Study of the Australian Positive & Peers Longevity Evaluation Study
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Secondary ID [1]
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2020-11-ARCHIVE
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Universal Trial Number (UTN)
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Trial acronym
ARCHIVE
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
HIV Infections
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Aging
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Condition category
Condition code
Infection
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Acquired immune deficiency syndrome (AIDS / HIV)
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Intervention/exposure
Study type
Observational [Patient Registry]
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
People with HIV over the age of 55 years -
People without HIV over the age of 55 years -
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Proportion of participants with at least one somatic mutation associated with clonal haematopoiesis
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Assessment method [1]
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Detection of mutations associated with clonal haematopoiesis
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Timepoint [1]
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2017-2019
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Secondary outcome [1]
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Median and natural log-transformed Interleukin-6
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Assessment method [1]
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Interleukin-6 level
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Timepoint [1]
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2017-2019
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Secondary outcome [2]
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Median (IQR) and natural log-transformed C-reactive protein and Cystatin C; D-dimer >0.27
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Assessment method [2]
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C-reactive protein, Cystatin C, D-dimer
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Timepoint [2]
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2017-2019
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Secondary outcome [3]
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Median (IQR) and natural log-transformed Haemoglobin
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Assessment method [3]
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Haemoglobin
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Timepoint [3]
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2017-2019
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Secondary outcome [4]
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Median (IQR) and natural log-transformed White blood cell count, Median (IQR) and natural log-transformed Neutrophil count, natural log-transformed Lymphocyte count, natural log-transformed platelet count
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Assessment method [4]
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White blood cell count, Neutrophil count, Lymphocyte count, platelet count
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Timepoint [4]
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2017-2019
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Secondary outcome [5]
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natural log-transformed Mean corpuscular volume
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Assessment method [5]
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mean corpuscular volume
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Timepoint [5]
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2017-2019
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Secondary outcome [6]
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natural log transformed Red Cell distribution width
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Assessment method [6]
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red cell distribution width
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Timepoint [6]
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2017-2019
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Secondary outcome [7]
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Proportion of participants with diagnosed cardiovascular conditions, any malignancy, haematologic malignancies
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Assessment method [7]
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Comorbid conditions
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Timepoint [7]
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2017-2019
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Eligibility
Key inclusion criteria
* Men and women aged >55
* For participants without HIV: an HIV negative test within 12 months prior to enrolment. If no HIV-negative test result is available within 12 months prior to enrolment, then participants will be tested for HIV as part of standard of care, if indicated by the guidelines for HIV testing published by the Australasian Society for HIV, Viral Hepatitis and Sexual Health Medicine14. This study will not conduct HIV testing; therefore, any participants without HIV being considered for participation in the study will need to have had a standard of care HIV negative test within the past 12 months. Some subjects at on-going risk for HIV are recommended to have periodic HIV testing and may be due for such testing as part of standard of care, at the time of enrolment into the study.
* Willing and able to provide written informed consent and willingness to participate in and comply with a longitudinal cohort study including 1) consent to providing blood samples for full blood count, inflammatory marker testing and genomics analysis 2) consent to linking their data to national and state-wide data registries (including consent to providing personally identifying information); and 3) consent to participate in future follow-up studies
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Minimum age
No limit
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
- Unwilling or unable to provide consent to participate
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Study design
Purpose
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Duration
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Selection
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
5/12/2017
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
4/12/2027
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Actual
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Sample size
Target
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Accrual to date
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Final
446
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Recruitment in Australia
Recruitment state(s)
NSW,VIC
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Recruitment hospital [1]
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St Vincent's Hospital HIV, Immunology and Infectious Disease Unit - Darlinghurst
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Recruitment hospital [2]
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Albion Street Centre - Sydney
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Recruitment hospital [3]
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East Sydney Doctors - Sydney
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Recruitment hospital [4]
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Holdsworth House Medical Practice - Sydney
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Recruitment hospital [5]
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Kirby Institute - Sydney
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Recruitment hospital [6]
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Taylor Square Private Clinic - Sydney
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Recruitment hospital [7]
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RPA Sexual Health, Royal Prince Alfred Hospital, Camperdown - Sydney
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Recruitment hospital [8]
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Alfred Hospital - Melbourne
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Recruitment hospital [9]
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Prahran Market Clinic - Melbourne
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Recruitment hospital [10]
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Monash Medical Centre - Melbourne
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Recruitment hospital [11]
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Peter MacCallum Cancer Centre - Melbourne
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Recruitment postcode(s) [1]
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2010 - Darlinghurst
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Recruitment postcode(s) [2]
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2010 - Sydney
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Recruitment postcode(s) [3]
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2050 - Sydney
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Recruitment postcode(s) [4]
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3004 - Melbourne
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Recruitment postcode(s) [5]
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3141 - Melbourne
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Recruitment postcode(s) [6]
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3168 - Melbourne
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Recruitment postcode(s) [7]
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- Melbourne
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Funding & Sponsors
Primary sponsor type
Government body
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Name
Kirby Institute
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Address
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Country
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Other collaborator category [1]
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Other
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Name [1]
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Peter MacCallum Cancer Centre, Australia
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Address [1]
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Country [1]
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Other collaborator category [2]
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Other
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Name [2]
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Holdsworth House Medical Centre
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Address [2]
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Country [2]
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Other collaborator category [3]
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Other
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Name [3]
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Prahran Market Clinic
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Address [3]
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Country [3]
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Other collaborator category [4]
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Other
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Name [4]
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East Sydney Doctors
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Address [4]
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Country [4]
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Other collaborator category [5]
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Other
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Name [5]
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RPA Sexual Health
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Address [5]
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Country [5]
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Other collaborator category [6]
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Other
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Name [6]
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The Alfred
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Address [6]
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Country [6]
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Other collaborator category [7]
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Other
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Name [7]
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St Vincent's Hospital
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Address [7]
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Country [7]
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Other collaborator category [8]
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Other
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Name [8]
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Taylor Square Medical Practice
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Address [8]
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Country [8]
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Other collaborator category [9]
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Other
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Name [9]
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Monash Health
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Address [9]
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Country [9]
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Other collaborator category [10]
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Other
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Name [10]
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Albion Street Clinic
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Address [10]
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Country [10]
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Ethics approval
Ethics application status
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Summary
Brief summary
The ARCHIVE study is an observational longitudinal cohort study of people with and without HIV who are over the age of 55. The duration of the study is planned for 10 years, with study visits every 1-2 years. The objectives of the study are to evaluate genomic and other factors associated with aging, stratified by HIV status.
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Trial website
https://clinicaltrials.gov/study/NCT04641013
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Trial related presentations / publications
Dharan NJ, Yeh P, Bloch M, Yeung MM, Baker D, Guinto J, Roth N, Ftouni S, Ognenovska K, Smith D, Hoy JF, Woolley I, Pell C, Templeton DJ, Fraser N, Rose N, Hutchinson J, Petoumenos K, Dawson SJ, Polizzotto MN, Dawson MA; ARCHIVE Study Group. HIV is associated with an increased risk of age-related clonal hematopoiesis among older adults. Nat Med. 2021 Jun;27(6):1006-1011. doi: 10.1038/s41591-021-01357-y. Epub 2021 Jun 7.
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Public notes
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Contacts
Principal investigator
Name
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Mark Polizzotto, MBBS, PhD
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Address
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Kirby Institute, UNSW Sydney
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for scientific queries
Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT04641013