A Non-Interventional Pilot Study to Explore the Role of Gut Flora in IBS

ProgenaBiome

Status: Withdrawn

Conditions: Irritable Bowel Syndrome Without Diarrhea; Irritable Bowel Syndrome; Irritable Bowel Syndrome With Constipation; Irritable Bowel Syndrome With Diarrhea; Irritable Bowel; Irritable Bowel Syndrome Characterized by Constipation; Irritable Bowel Syndrome Characterised by Alternating Bowel Habit; Irritable Bowel Syndrome Mixed; Irritable Bowel Syndrome Aggravated

Treatments: Other: No intervention

Study type: Observational

Funder types: Other

Identifiers

NCT04214470

PRG-036

Details and patient eligibility

About

This study seeks to correlate microbiome sequencing data with information provided by patients and their medical records.

Full description

The goal of this Research Study is to better understand how the genetic information in subject's microbiome correlates to IBS.

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Signed informed consent, demonstrating that the patient understands the procedures required for the study and the purpose of the study

   a. May be signed by parent or legal guardian in the case of minor or adult unable to provide consent

2. Male or female of all ages

3. Diagnosis of IBS

Exclusion criteria

1. Refusal to sign informed consent form
2. History of bariatric surgery, total colectomy with ileorectal anastomosis or proctocolectomy.
3. Postoperative stoma, ostomy, or ileoanal pouch
4. Participation in any experimental drug protocol within the past 12 weeks
5. Treatment with total parenteral nutrition

Trial design

0 participants in 1 patient group

Irritable Bowel Syndrome Patients

Description:

Patients with IBS.

Treatment:

Other: No intervention