Register a trial

The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT03849716




Registration number
NCT03849716
Ethics application status
Date submitted
17/01/2019
Date registered
21/02/2019

Titles & IDs
Public title
Evaluation of Biomarkers of Atopic Dermatitis in Pediatric Patients (PEDISTAD BIOMARKER STUDY)
Scientific title
Evaluation of Biomarkers of Atopic Dermatitis in Pediatric Patients Whose Disease is Not Adequately Controlled With Topical Prescription Therapies or When Those Therapies Are Not Medically Advisable
Secondary ID [1] 0 0
U1111-1207-8876
Secondary ID [2] 0 0
LPS15496
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Dermatitis Atopic 0 0
Condition category
Condition code
Skin 0 0 0 0
Dermatological conditions
Skin 0 0 0 0
Other skin conditions
Inflammatory and Immune System 0 0 0 0
Other inflammatory or immune system disorders

Intervention/exposure
Study type
Observational [Patient Registry]
Patient registry
Target follow-up duration
Target follow-up type
Description of intervention(s) / exposure
Other interventions - Blood sample
Other interventions - Cheek swab

Participants with atopic dermatitis (AD) - Participants included in observational study OBS15333 (atopic dermatitis pediatric registry) who consent to enter this companion study LPS15496. Participants receive AD therapy as part of their usual care as determined by their physician independent of decision to enter either protocol, and neither protocol OBS15333 nor LPS15496 specifies assignment of any drug intervention


Other interventions: Blood sample
Blood samples obtained for biomarker analyses

Other interventions: Cheek swab
Cheek swab obtained for genetic analysis
Intervention code [1] 0 0
Other interventions
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Biomarker identification: Demographics
Timepoint [1] 0 0
Baseline
Primary outcome [2] 0 0
Biomarker identification: Baseline disease characteristics
Timepoint [2] 0 0
Baseline
Primary outcome [3] 0 0
Biomarker identification: Changes in disease severity
Timepoint [3] 0 0
Up to 5 years
Primary outcome [4] 0 0
Biomarker evaluation: High versus low disease severity across participants
Timepoint [4] 0 0
Up to 5 years
Primary outcome [5] 0 0
Biomarker identification: New presentation or resolution of atopic comorbidity
Timepoint [5] 0 0
Up to 5 years
Primary outcome [6] 0 0
Biomarker identification: Introduction of new systemic treatment
Timepoint [6] 0 0
Up to 5 years
Primary outcome [7] 0 0
Biomarker identification: Response to systemic treatment
Timepoint [7] 0 0
Up to 5 years
Primary outcome [8] 0 0
Biomarker identification: Loss of response to systemic treatment
Timepoint [8] 0 0
Up to 5 years
Primary outcome [9] 0 0
Biomarker evaluation: Start of systemic therapy early in life versus later in life
Timepoint [9] 0 0
Up to 5 years

Eligibility
Key inclusion criteria
Inclusion criteria:

* Participation in the OBS15333 pediatric atopic dermatitis (AD) registry.
* Signed informed consent by the parent/legally acceptable representative and assent by the participant appropriate to the participant's age.
Minimum age
0 Years
Maximum age
11 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Exclusion criteria:

Not applicable.

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Study design
Purpose
Duration
Selection
Timing
Prospective
Statistical methods / analysis

Recruitment
Recruitment status
Active, not recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
5/04/2019
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
30/09/2026
Actual
Sample size
Target
Accrual to date
Final
266
Recruitment in Australia
Recruitment state(s)
NSW,VIC
Recruitment hospital [1] 0 0
Investigational Site Number : 0360001 - Westmead
Recruitment hospital [2] 0 0
Investigational Site Number : 0360003 - Melbourne
Recruitment postcode(s) [1] 0 0
2145 - Westmead
Recruitment postcode(s) [2] 0 0
3010 - Melbourne
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Alabama
Country [2] 0 0
United States of America
State/province [2] 0 0
California
Country [3] 0 0
United States of America
State/province [3] 0 0
Florida
Country [4] 0 0
United States of America
State/province [4] 0 0
Georgia
Country [5] 0 0
United States of America
State/province [5] 0 0
Illinois
Country [6] 0 0
United States of America
State/province [6] 0 0
New York
Country [7] 0 0
United States of America
State/province [7] 0 0
Ohio
Country [8] 0 0
United States of America
State/province [8] 0 0
South Carolina
Country [9] 0 0
United States of America
State/province [9] 0 0
Texas
Country [10] 0 0
Argentina
State/province [10] 0 0
Buenos Aires
Country [11] 0 0
Argentina
State/province [11] 0 0
Santa Fe
Country [12] 0 0
Argentina
State/province [12] 0 0
Ciudad Autonoma Bs As
Country [13] 0 0
Brazil
State/province [13] 0 0
Paraná
Country [14] 0 0
Brazil
State/province [14] 0 0
Rio Grande Do Sul
Country [15] 0 0
Brazil
State/province [15] 0 0
São Paulo
Country [16] 0 0
Brazil
State/province [16] 0 0
Sorocaba
Country [17] 0 0
Canada
State/province [17] 0 0
Alberta
Country [18] 0 0
Canada
State/province [18] 0 0
Manitoba
Country [19] 0 0
Canada
State/province [19] 0 0
Ontario
Country [20] 0 0
Canada
State/province [20] 0 0
Quebec
Country [21] 0 0
Colombia
State/province [21] 0 0
Bogota
Country [22] 0 0
France
State/province [22] 0 0
Marseille cedex 5
Country [23] 0 0
France
State/province [23] 0 0
Paris Cedex 15
Country [24] 0 0
Mexico
State/province [24] 0 0
Nuevo León
Country [25] 0 0
Mexico
State/province [25] 0 0
Mexico
Country [26] 0 0
Mexico
State/province [26] 0 0
Tlalnepantla
Country [27] 0 0
Netherlands
State/province [27] 0 0
Groningen
Country [28] 0 0
Netherlands
State/province [28] 0 0
Utrecht

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Sanofi
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Clinical Sciences & Operations
Address 0 0
Sanofi
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


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/NCT03849716