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Registry for Women Who Are At Risk Or May Have Lynch Syndrome

NCT00508573 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 323

Last updated 2024-08-09

No results posted yet for this study

Summary

The goal of this study is to create a registry of information about women who have or are at risk for Lynch syndrome, in order to study gynecologic cancer risks.

This is an investigational study. Up to 1000 patients will take part in this study. All patients will be enrolled at MD Anderson.

Conditions

Interventions

BEHAVIORAL

Questionnaire

Follow-up questionnaire done once a year for five years.

Sponsors & Collaborators

  • M.D. Anderson Cancer Center

    lead OTHER

Principal Investigators

  • Karen H. Lu, MD · M.D. Anderson Cancer Center

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-05-31
Primary Completion
2024-08-05
Completion
2024-08-05

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT00508573 on ClinicalTrials.gov