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

Withdrawn before enrolling

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

In brief

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

Key facts

Study ID

NCT04214470

Run by

ProgenaBiome

People needed

0

Starts

2020-03-02

Expected to finish

2030-07-01

Last updated by the study team

2025-06-05

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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
• Male or female of all ages
• Diagnosis of IBS

You may not qualify if…

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

Where it is running

• ProgenaBiome — Ventura, California, United States

Full record on ClinicalTrials.gov

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