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Combined Colon and Endometrial Cancer Screening in Women With HNPCC

A Pilot Study for Combined Colon and Endometrial Cancer Screening in Women at High-Risk for Colon and Endometrial Cancer

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00510796
Enrollment
50
Registered
2007-08-02
Start date
2002-03-31
Completion date
2015-12-31
Last updated
2016-02-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colon Cancer

Keywords

Hereditary Non-Polyposis Colon Cancer, Colon Cancer, Endometrial Cancer, Cancer Screening, Interview, HNPCC

Brief summary

Primary Objectives: To test the feasibility of combined colon and endometrial cancer screening in women with increased risk for colon and endometrial cancer. To measure patient satisfaction for the combined procedure.

Detailed description

Women with certain medical conditions have an increased risk for colon and endometrial cancer. Currently, women go through separate screening procedures. Endometrial biopsies are performed at a separate visit to the gynecologist, and patients are not sedated for the procedure. This study will involve performing an endometrial biopsy while you are sedated for your colonoscopy. Women who are able to have children must have a negative blood or urine pregnancy test before they can take part in this study. As part of the study, you will be asked about your past experience with endometrial biopsy and colonoscopy. You will be asked about your perception of pain, your expectations, and the benefits and barriers to the combined screening. You will then be sedated. The colonoscopy will be performed first by a gastroenterologist. This will be followed by the endometrial biopsy, which will be performed by a gynecologic oncologist. A telephone interview will be performed two weeks after this procedure. The interview will last about 15 minutes. You will be asked about your perception of pain and the benefits and barriers to the combined screening. This is an investigational study. A total of 50 women will take part in this study. All will be enrolled at M. D. Anderson.

Interventions

BEHAVIORALInterview

Interview regarding perception of pain and the benefits and barriers to the combined screening.

Sponsors

M.D. Anderson Cancer Center
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1\) Women with medical indications for colonoscopy and endometrial biopsy.

Exclusion criteria

1\) Must be 18 years of age and older.

Design outcomes

Primary

MeasureTime frame
Feasibility to perform both colon and endometrial cancer screening at the time of colonoscopy in women at high risk for colon and endometrial cancer.8 Years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026