Purpose

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

Conditions

Eligibility

Eligible Ages
Over 12 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

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 of any age (interest is given to children 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

Study Design

Phase
Study Type
Observational
Observational Model
Other
Time Perspective
Other

Arm Groups

ArmDescriptionAssigned Intervention
General Population The general population will have their microbiome sequenced from stool samples provided.
  • Other: There is no intervention in this study
    There is no intervention in this study

Recruiting Locations

More Details

Status
Recruiting
Sponsor
ProgenaBiome

Study Contact

Sabine Hazan, MD
18053390549
drsabinehazan@progenabiome.com

Detailed Description

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.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.