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


N/A
18 Years
N/A
Open (Enrolling)
Female
Colon Cancer

Thank you

Trial Information

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


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.


Inclusion Criteria:



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

Exclusion Criteria:

1) Must be 18 years of age and older.

Type of Study:

Observational

Study Design:

Observational Model: Case-Only, Time Perspective: Prospective

Outcome Measure:

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

Outcome Time Frame:

8 Years

Safety Issue:

No

Principal Investigator

Karen H. Lu, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

M.D. Anderson Cancer Center

Authority:

United States: Institutional Review Board

Study ID:

ID01-694

NCT ID:

NCT00510796

Start Date:

March 2002

Completion Date:

Related Keywords:

  • Colon Cancer
  • Hereditary Non-Polyposis Colon Cancer
  • Colon Cancer
  • Endometrial Cancer
  • Cancer Screening
  • Interview
  • HNPCC
  • Colonic Neoplasms
  • Endometrial Neoplasms
  • Adenoma

Name

Location

UT MD Anderson Cancer Center Houston, Texas  77030