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

Clinical Trial ID: NCT04031469

Description

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

The goal of this Research Study is to better understand how the genetic information in subject's microbiome correlates to the information provided in surveys and in medical records.


Criteria

Inclusion Criteria: - 1. Signed informed consent, demonstrating that the patient understands the procedures required for the study and the purpose of the study - 2. Male or female patients age 12 and older. ( interest is given to children 12 and older to compare with mothers). 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 - 6. Any clinically significant evidence of disease that could interfere with the subject's ability to enter the trial - 7. Inability to adequately communicate with the investigator or their respective designee and/or comply with the requirements of the entire study

  • Start Date

    2019-07-11

  • Last Updated

    2019-07-31

  • Sponsor

    ProgenaBiome

  • Condition Name

    Gastrointestinal Microbiome

Learn about this trial.

Check the eligibility requirements, study details, and more.

Related Trials

Different trials target different symptoms, condition types, and patients. Learn more about other emergeing treatments being investigated now.