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

  • STATUS
    Recruiting
  • participants needed
    100
  • sponsor
    ProgenaBiome
Updated on 19 February 2024

Summary

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

Description

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

Details
Condition 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
Age 100 years and younger
Treatment No intervention
Clinical Study IdentifierNCT04214470
SponsorProgenaBiome
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

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

Exclusion Criteria

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
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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