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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04203303
Other study ID # 19-001234
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 3, 2019
Est. completion date December 31, 2030

Study information

Verified date January 2024
Source Mayo Clinic
Contact Shahid Karim
Phone (507) 422-0763
Email Karim.Shahid@mayo.edu
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The purpose of this study is to advance the understanding of human health and disease as it relates to environmental factors that may affect intestinal and non-intestinal microbiota.


Recruitment information / eligibility

Status Recruiting
Enrollment 5000
Est. completion date December 31, 2030
Est. primary completion date October 15, 2030
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age 18 years of age or older - Able to provide informed consent Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Observational
Observational

Locations

Country Name City State
United States Mayo Clinic Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Microbiome Differences compare the relative abundance of specific microorganism groups 10 years
See also
  Status Clinical Trial Phase
Terminated NCT02948192 - The Reproductive Microbiome & Perinatal Health Outcomes

External Links