Changes in Gastrointestinal Microbiota Using VSL#3 in Patients With IBS-D
Primary Purpose
Irritable Bowel Syndrome
Status
Unknown status
Phase
Phase 4
Locations
India
Study Type
Interventional
Intervention
VSL#3
Sponsored by
About this trial
This is an interventional treatment trial for Irritable Bowel Syndrome
Eligibility Criteria
Inclusion Criteria:
- Patients satisfying Rome III Criteria
Exclusion Criteria:
- Antimicrobial medication during last 2 months
- Probiotics medication during last 2 months
- Pregnant or lactating patients
- Previous major or complicated abdominal surgery
- Positive test for HIV, HBV or HCV
Sites / Locations
- Asian Institute of Gstroenterology
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
VSL#3
Healthy Controls
Arm Description
Patients with IBS-D as per ROME III
Healthy controls
Outcomes
Primary Outcome Measures
Improvement of symptoms after modulation of gut microbiota with probiotic, VSL#3
To study modulation of gut microbiota profile after treatment with probiotics (VSL #3) for 8 weeks.
Secondary Outcome Measures
Comparison of GI microbiota before and after treatment
To characterize type of bacterial species and compare diversity of the host's gut microbiota in 20 Irritable bowel syndrome (IBS) patients with 16 healthy controls (HCs) using high through put culture-independent method like Illumina sequencing.
Full Information
NCT ID
NCT01638208
First Posted
July 6, 2012
Last Updated
July 9, 2012
Sponsor
Asian Institute of Gastroenterology, India
1. Study Identification
Unique Protocol Identification Number
NCT01638208
Brief Title
Changes in Gastrointestinal Microbiota Using VSL#3 in Patients With IBS-D
Official Title
Spectrum of Gastrointestinal Microbiota in Patients With IBS-D Before and After Treatment With VSL#3.
Study Type
Interventional
2. Study Status
Record Verification Date
July 2012
Overall Recruitment Status
Unknown status
Study Start Date
August 2012 (undefined)
Primary Completion Date
December 2012 (Anticipated)
Study Completion Date
December 2012 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Asian Institute of Gastroenterology, India
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Aim
To compare changes in gut microbiota of IBS patients and healthy controls using next generation sequencing method like Illumina sequencing based on 16S rDNA profiling.
The major objectives of the study are:
To characterize type of bacterial species and compare diversity of the host's gut microbiota in 20 Irritable bowel syndrome (IBS) patients with 16 healthy controls (HCs) using high through put culture-independent method like Illumina sequencing.
To study modulation of gut microbiota profile after treatment with probiotics (VSL #3) for 8 weeks.
To study the improvement of symptoms after modulation of gut microbiota with probiotics (VSL #3) for more than 8 weeks.
Detailed Description
Introduction
The role of the commensal flora in many disease states, including irritable bowel syndrome, inflammatory bowel disease, and even obesity, is now accepted and will undoubtedly lead to new therapeutic strategies. The recently NIH-initiated Human Microbiome Project will allow better understanding of the role of this complex intestinal community in human health and disease. On the clinical side, we are exploring the more common pathogenic bacterial strains in Irritable bowel syndrome patients and use of probiotics in this functional gastrointestinal disease. We are taking support from Genotypic institute, Bangalore for Illumina sequencing facility.
Asian Institute of Gastroenterology, the parent institution, is a 200 bed tertiary care referral hospital providing services to patients with GI diseases, with a daily attendance of 400 out-patients and 200 in-patients. The long term goals of the investigators, involving basic researchers and clinicians, include development of technological resources and applications of biotechnology for use in clinical trials to improve survival rates of patients with GI diseases. The major volume of the outpatient cases comprise of patients with irritable bowel syndrome. Altered GI microbiota may contribute to IBS symptoms and studying dysbiosis in gut microbiota is an important to develop therapy for IBS.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Irritable Bowel Syndrome
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
VSL#3
Arm Type
Experimental
Arm Description
Patients with IBS-D as per ROME III
Arm Title
Healthy Controls
Arm Type
No Intervention
Arm Description
Healthy controls
Intervention Type
Drug
Intervention Name(s)
VSL#3
Other Intervention Name(s)
probiotic
Intervention Description
Dosage Form: Capsules (Details as given below); Dose and duration of treatment: 1 capsule b.i.d for 8 weeks; Each capsule contains 112.5 Billion CFU of the following 8 strains of bacteria, 4 lactobacilli strains (L. acidophilus, L. plantarum, L. paracasei, L. delbrueckii subsp bulgaricus), 3 bifidobacteria strains (B. breve, B. infantis, B. longum) and 1 strain of S. thermophilus).
Primary Outcome Measure Information:
Title
Improvement of symptoms after modulation of gut microbiota with probiotic, VSL#3
Description
To study modulation of gut microbiota profile after treatment with probiotics (VSL #3) for 8 weeks.
Time Frame
8 wks
Secondary Outcome Measure Information:
Title
Comparison of GI microbiota before and after treatment
Description
To characterize type of bacterial species and compare diversity of the host's gut microbiota in 20 Irritable bowel syndrome (IBS) patients with 16 healthy controls (HCs) using high through put culture-independent method like Illumina sequencing.
Time Frame
8 wks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients satisfying Rome III Criteria
Exclusion Criteria:
Antimicrobial medication during last 2 months
Probiotics medication during last 2 months
Pregnant or lactating patients
Previous major or complicated abdominal surgery
Positive test for HIV, HBV or HCV
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dr. Nitesh Pratap, DM
Phone
0091-9000150678
Email
pratapnitesh@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Nitesh Pratap, DM
Organizational Affiliation
Asian Institute of Gastroenterology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Dr. Nageshwar Reddy, DM
Organizational Affiliation
Asian Institute of Gastroenterology
Official's Role
Study Director
Facility Information:
Facility Name
Asian Institute of Gstroenterology
City
Hyderabad
State/Province
Andhra Pradesh
ZIP/Postal Code
500082
Country
India
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dr. Nitesh Pratap, DM
Phone
0091-9000150678
Email
pratapnitesh@yahoo.com
First Name & Middle Initial & Last Name & Degree
Dr. Nitesh Pratap, DM
First Name & Middle Initial & Last Name & Degree
Dr. Nageshwar Reddy, DM
12. IPD Sharing Statement
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Changes in Gastrointestinal Microbiota Using VSL#3 in Patients With IBS-D
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