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Changes in Gastrointestinal Microbiota Using VSL#3 in Patients With IBS-D

A

Asian Institute of Gastroenterology, India

Status and phase

Unknown
Phase 4

Conditions

Irritable Bowel Syndrome

Treatments

Drug: VSL#3

Study type

Interventional

Funder types

Other

Identifiers

NCT01638208
AIG-VSL#3-IBS-NP

Details and patient eligibility

About

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.

Full 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.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

40 participants in 2 patient groups

VSL#3
Experimental group
Description:
Patients with IBS-D as per ROME III
Treatment:
Drug: VSL#3
Healthy Controls
No Intervention group
Description:
Healthy controls

Trial contacts and locations

1

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Central trial contact

Dr. Nitesh Pratap, DM

Data sourced from clinicaltrials.gov

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