Observational Study of Sub-populations From Cologuard Post-Approval Study (2014-01)

NCT03705013 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 51

Last updated 2020-04-14

No results posted yet for this study

Summary

The primary endpoint is to obtain longitudinal information on four sub-populations from the Cologuard Post-Approval Study.

Conditions

Interventions

OTHER

Cologuard

Observational

Sponsors & Collaborators

  • Exact Sciences Corporation

    lead INDUSTRY

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-10-30
Primary Completion
2019-11-16
Completion
2019-11-16

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03705013 on ClinicalTrials.gov