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Trial registered on ANZCTR
Registration number
ACTRN12613000910707
Ethics application status
Approved
Date submitted
11/08/2013
Date registered
15/08/2013
Date last updated
2/05/2014
Type of registration
Retrospectively registered
Titles & IDs
Public title
Effect of sustained release baclofen on alleviation of gastro-esophageal reflux disease symptoms
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Scientific title
Effect of Baclofen sustained release vs placebo on alleviation of reflux symptoms in patients with Gastroesophageal reflux disease
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Secondary ID [1]
283001
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nil
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Gastroesophageal reflux disease
289828
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Condition category
Condition code
Oral and Gastrointestinal
290185
290185
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0
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Addition of oral tablet baclofen sustained release 10 mg twice daily or placebo twice daily for 1 months to the selective treatment of Gastroesophageal reflux disease in Iranian clinics(oral omeprazole 20 mg/d for 2 months). Baclofen/placebo and omeprazole will be start at the same time.
Adherence monitoring by pill count
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Intervention code [1]
287716
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Treatment: Drugs
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Comparator / control treatment
placebo contains microcellulose tablet
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Control group
Placebo
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Outcomes
Primary outcome [1]
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alleviation of gastroesophagear reflux disesase symptoms by Mayo Gastro-esophageal Reflux questionnaire
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Assessment method [1]
290215
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Timepoint [1]
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1 month
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Secondary outcome [1]
304123
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alleviation of quality of life by SF-36 Quality of Life Questionnaire
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Assessment method [1]
304123
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Timepoint [1]
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1 month
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Eligibility
Key inclusion criteria
patients with diagnosis of Gastroesophageal reflux disease on the basis of Rome 3 criteria
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Minimum age
18
Years
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Maximum age
60
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
1.history of Hypersensivity to baclofen
2.renal or hepatic failure
3.Neurological diseases
4.pregnant women
5.breastfeeding women
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
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Type of endpoint/s
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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
14/01/2013
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Actual
14/06/2013
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Date of last participant enrolment
Anticipated
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Actual
10/01/2014
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
40
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
5290
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Iran, Islamic Republic Of
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State/province [1]
5290
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Tehran
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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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Shahid Beheshti University of Medical Sciences
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Address [1]
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Velenjak, near Talighani hospital, 3rd street, Tehran,Tehran, Iran PO box: 14397-65461
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Country [1]
287768
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Iran, Islamic Republic Of
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Primary sponsor type
University
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Name
Shahid Beheshti University of Medical Sciences
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Address
Velenjak, near Talighani hospital, 3rd street, Tehran,Tehran, Iran PO box: 14397-65461
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Country
Iran, Islamic Republic Of
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Secondary sponsor category [1]
286495
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None
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Name [1]
286495
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Address [1]
286495
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Country [1]
286495
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
289715
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Ethics commiittee, Shahid Beheshti University of Medical sciences
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Ethics committee address [1]
289715
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Velenjak, near Talighani hospital, 3rd street, Tehran,Tehran, Iran PO box: 14397-65462
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Ethics committee country [1]
289715
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Iran, Islamic Republic Of
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Date submitted for ethics approval [1]
289715
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08/02/2013
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Approval date [1]
289715
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01/03/2013
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Ethics approval number [1]
289715
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576-98234
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Summary
Brief summary
Proton Pump Inhibitors(PPIs) such as omeprazole are primary treatment for gastroesophageal reflux disease(GERD). Some patients do not cure adequetly with using PPIs. So we want to try effect of addition baclofen sustained release 10 mg twice daily vs placebo in addition to omeprazole 20 mg/d in both groups in alleviation of gastroesophageal reflux symptoms.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr Mohammad Abbasinazari
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Address
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Velenjak, near Talighani hospital, 3rd street, Tehran,Tehran, Iran, Shahid Beheshti University of Medical Sciences PO box: 14397-65461
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Country
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Iran, Islamic Republic Of
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Phone
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+98 2188873704
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Fax
42098
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Email
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[email protected]
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Contact person for public queries
Name
42099
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Mohammad Abbasinazari
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Address
42099
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Velenjak, near Talighani hospital, 3rd street, Tehran,Tehran, Iran, Shahid Beheshti University of Medical Sciences PO box: 14397-65461
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Country
42099
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Iran, Islamic Republic Of
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Phone
42099
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+98 2188873704
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Fax
42099
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Email
42099
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[email protected]
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Contact person for scientific queries
Name
42100
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Mohammad Abbasinazari
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Address
42100
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Velenjak, near Talighani hospital, 3rd street, Tehran,Tehran, Iran, Shahid Beheshti University of Medical Sciences PO box: 14397-65461
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Country
42100
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Iran, Islamic Republic Of
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Phone
42100
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+98 2188873704
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Fax
42100
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Email
42100
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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
No additional documents have been identified.
Download to PDF