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

P

ProgenaBiome

Status

Unknown

Conditions

Anxiety Depression
Anxiety Disorders
Anxiety

Treatments

Other: No Intervention

Study type

Observational

Funder types

Other

Identifiers

NCT04211376
PRG-028

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 anxiety

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

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 anxiety based on DSM-V criteria

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

100 participants in 1 patient group

Anxiety
Description:
Patients with anxiety
Treatment:
Other: No Intervention

Trial contacts and locations

1

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Central trial contact

Jordan Daniels, MS; Sabine Hazan, MD

Data sourced from clinicaltrials.gov

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