Trial Review

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 registered on ANZCTR


Registration number
ACTRN12610001066077
Ethics application status
Approved
Date submitted
28/11/2010
Date registered
3/12/2010
Date last updated
3/12/2010
Type of registration
Retrospectively registered

Titles & IDs
Public title
Blastocystis subtypes in symptomatic and asymptomatic family members and pets and response to therapy.
Scientific title
In people positive for Blastocystis carriage in their stools is their any difference in the specific Blastocystis subtypes found between patients with gastrointestinal symptoms and their asymptomatic human and animal household members and do their gastrointestinal symptoms change after therapy with metronidazole or sulfamethoxazole/trimethoprim.
Secondary ID [1] 253225 0
University of Queensland, School of Veterinary Science, Gatton
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Irritable bowel like gastrointestinal symptoms in patients positive for Blastocystis carriage in their stool. 258726 0
Response of symptomatic patients positive for Blastocystis to 14 days of therapy with metronidazole 400 mg three times daily or sulfamethoxazole/trimethoprim 160mg/800mg twice daily. 258727 0
Specific subtypes of Blastocystis found in symptomatic patients compared to asymptomatic human and animal household members. 258728 0
Condition category
Condition code
Oral and Gastrointestinal 258879 258879 0 0
Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Patients with gastrointestinal symptoms positive for Blastocystis carriage in their stool were treated with 14 days of either oral metronidazole 400 mg three times daily or oral sulfamethoxazole/trimethoprim (Bactrim) 160/800 mg twice daily.
Intervention code [1] 257676 0
Treatment: Drugs
Comparator / control treatment
Faecal samples were collected from symptomatic patients before and within 48 hours of cessation of antibiotic therapy and again at Day 28 and 56 after therapy. The patient pre-treatment is acting as his/her own control.
Control group
Active

Outcomes
Primary outcome [1] 259738 0
Presence or absence of Blastocystis in stool samples before and after antibiotic therapy as assessed by fresh faecal smears, faecal culture and PCR analysis of both faecal specimens and faecal cultures.
Timepoint [1] 259738 0
Sample time points were baseline (0-2 weeks before therapy), Day 15, 28 and 56.
Secondary outcome [1] 266474 0
To assess how many asymptomatic human and animal household contacts of symptomatic patients were also positive for Blastocystis in their stool and to assess if there was any difference in Blastocystis subtypes between symptomatic and asymptomatic carriers.
Timepoint [1] 266474 0
Faecal samples were assessed at Day 15 in these groups with fresh faecal smears, faecal cultures and PCR analysis of both faeces and faecal cultures.

Eligibility
Key inclusion criteria
Chronic gastrointestinal symptoms
Minimum age
16 Years
Maximum age
80 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Other documented cause of gastrointestinal symptoms other than Blastocystis carriage

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Not Applicable
Type of endpoint/s
Safety/efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
9/04/2008
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
10
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)

Funding & Sponsors
Funding source category [1] 258150 0
University
Name [1] 258150 0
University of Queensland
Country [1] 258150 0
Australia
Primary sponsor type
Individual
Name
Dr Rebecca Traub
Address
School of Veterinary Science,
University of Queensland,
Building 8114
Gatton Campus,
Gatton
Queensland, 4343
Country
Australia
Secondary sponsor category [1] 257315 0
None
Name [1] 257315 0
Address [1] 257315 0
Country [1] 257315 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 260127 0
University of Queensland Medical Research Ethics Committee
Ethics committee address [1] 260127 0
Ethics committee country [1] 260127 0
Australia
Date submitted for ethics approval [1] 260127 0
Approval date [1] 260127 0
09/04/2008
Ethics approval number [1] 260127 0

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

Contacts
Principal investigator
Name 31962 0
Address 31962 0
Country 31962 0
Phone 31962 0
Fax 31962 0
Email 31962 0
Contact person for public queries
Name 15209 0
Robyn Nagel
Address 15209 0
Unit 105, Medici Medical Centre
11 Scott St
Toowoomba,
Queensland
4350
Country 15209 0
Australia
Phone 15209 0
+61 7 46394124
Fax 15209 0
+61 7 46394070
Email 15209 0
[email protected]
Contact person for scientific queries
Name 6137 0
Robyn Nagel
Address 6137 0
Unit 105, Medici Medical Centre
11 Scott St
Toowoomba
Queensland, 4350
Country 6137 0
Australia
Phone 6137 0
+61 7 46394124
Fax 6137 0
+61 7 46394070
Email 6137 0
[email protected]

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
No additional documents have been identified.