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A Non-Interventional Pilot Study to Explore the Role of Gut Flora in Obsessive-Compulsive Disorder

P

ProgenaBiome

Status

Withdrawn

Conditions

Obsessive-Compulsive Disorder

Treatments

Other: No Intervention

Study type

Observational

Funder types

Other

Identifiers

NCT04211402
PRG-029

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 infection with Obsessive-Compulsive Disorder.

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. OCI greater than or equal to 21

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

Obsessive-Compulsive Disorder
Description:
Patients with obsessive-compulsive disorder
Treatment:
Other: No Intervention

Trial contacts and locations

1

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Central trial contact

Sabine Hazan, MD; Jordan Daniels, MS

Data sourced from clinicaltrials.gov

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