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Trial registered on ANZCTR
Registration number
ACTRN12611000918921
Ethics application status
Approved
Date submitted
2/08/2011
Date registered
29/08/2011
Date last updated
18/07/2018
Type of registration
Retrospectively registered
Titles & IDs
Public title
Efficacy of Triple Antibiotic Therapy in Symptomatic Blastocystis patients
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Scientific title
In patients with symptomatic Blastocystis, is triple antibiotic therapy effective in clearing Blastocystis from the stool and improving clinical well-being?
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Secondary ID [1]
262909
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Nil known
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Universal Trial Number (UTN)
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Trial acronym
Nil
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Blastocystis infection
270473
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Condition category
Condition code
Oral and Gastrointestinal
270627
270627
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0
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Inflammatory bowel disease
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Infection
270798
270798
0
0
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Other infectious diseases
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Administration of 14 days of oral capsule antibiotics: specifically trimethoprim/sulfamethoxazole 160/800mg twice daily, diloxanide furoate 500 mg three times daily and secnidazole 400mg three times daily
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Intervention code [1]
267106
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Treatment: Drugs
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Comparator / control treatment
Before and after; No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Clearance of Blastocystis from stool specimen
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Assessment method [1]
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Timepoint [1]
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Baseline, 15 day and 6 weeks after 14 days of antibiotic therapy
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Secondary outcome [1]
279442
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Improvement in clinical well being; patient diary
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Assessment method [1]
279442
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Timepoint [1]
279442
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baseline, day 15 and week 6 after antibiotic therapy
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Eligibility
Key inclusion criteria
Gastrointestinal symptoms
No other cause except Blastocystis found on investigation
Good general health
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Minimum age
18
Years
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Maximum age
70
Years
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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
Allergy to Sulphurs
Pregnancy or risk of pregnancy
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Exclusion of other causes of gastrointestinal symptoms with clinical history, examination, routine blood tests and stool cultures and an upper and lower endoscopy.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Phase 3
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/08/2011
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Actual
9/08/2011
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Date of last participant enrolment
Anticipated
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Actual
20/02/2014
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Date of last data collection
Anticipated
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Actual
24/04/2014
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Sample size
Target
10
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Accrual to date
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Final
10
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Recruitment in Australia
Recruitment state(s)
QLD
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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School of Veterinary Science, University of Queensland
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Address [1]
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Building 8114,
Gatton Campus
Warrego Hwy,
Gatton
QLD, 4352
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Country [1]
269584
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Australia
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Primary sponsor type
University
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Name
University of Queensland
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Address
School of Veterinary Science
University of Queensland
Gatton Campus
Warrego Hwy
Gatton, QLD
4352
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Country
Australia
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Secondary sponsor category [1]
266618
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Individual
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Name [1]
266618
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Dr Robyn Nagel
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Address [1]
266618
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Suite 105, Medici Medical Centre
11 Scott St
Toowoomba,
QLD
4350
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Country [1]
266618
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Medical research Ethics Committee University of Queensland
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Ethics committee address [1]
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University of Queensland Cumbrae-Stewart Building Research Rd Brisbane, Qld 4072
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Ethics committee country [1]
269537
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Australia
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Date submitted for ethics approval [1]
269537
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Approval date [1]
269537
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02/06/2011
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Ethics approval number [1]
269537
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2011000454
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Summary
Brief summary
We intend to evaluate the efficacy of 14 days of the triple antibiotics listed above in eradicating Blastocystis infection in symptomatic patients.
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Trial website
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Trial related presentations / publications
"Clinical pilot study: Efficacy of triple antibitoic therqpy in Blastocystis positive irritble bowel syndrome patients" R Nagel, H Bielefeldt-Ohmann, R Traub Gut Pathogens 6 (1), 34, 2014
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Public notes
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Contacts
Principal investigator
Name
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Dr Robyn Nagel
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Address
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Toowoomba Gastroenterology Clinic
Suite 105, Medici Medical Centre
15 Scott St
Toowoomba
Queensland 4350
Australia
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Country
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Australia
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Phone
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+61 7 46394134
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Dr Robyn Nagel
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Address
16214
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Suite 105, Medici Medical Centre
11 Scott St
Toowoomba,
QLD
4350
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Country
16214
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Australia
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Phone
16214
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+61 7 46394124
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Fax
16214
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+61 7 46394070
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Email
16214
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[email protected]
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Contact person for scientific queries
Name
7142
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Dr Robyn Nagel
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Address
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Suite 105, Medici Medical Centre
11 Scott St
Toowoomba
QLD
4350
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Country
7142
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Australia
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Phone
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+61 7 46394124
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Fax
7142
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+61 7 46394070
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Email
7142
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Blastocystis specific serum immunoglobulin in patients with irritable bowel syndrome (IBS) versus healthy controls.
2015
https://dx.doi.org/10.1186/s13071-015-1069-x
N.B. These documents automatically identified may not have been verified by the study sponsor.
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