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NCT00791635 · ClinicalTrials.gov registry record
Longitudinal Evaluation of Women Undergoing Pelvic Surgery for the Treatment of Gynecologic Cancer
A clinical trial of Endometrial Carcinoma and Cervical Carcinoma, sponsored by M.D. Anderson Cancer Center.
- Active
- Registry status
- 79
- Enrollment target
- 1
- Study location
NCT00791635 is a study of Endometrial Carcinoma and Cervical Carcinoma that is active but no longer recruiting, run by M.D. Anderson Cancer Center. The registered enrollment target is 79 participants, below the 388-participant average among 27 other Endometrial Carcinoma trials with a reported enrollment target (80% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00791635, a study of Endometrial Carcinoma and Cervical Carcinoma, is active but no longer recruiting, sponsored by M.D. Anderson Cancer Center.
- ACTIVE NOT RECRUITING
- Registry status
- 79 participants
- Enrollment target
- 1
- Study location
Study Summary
The study investigates whether certain characteristics of gynecological cancer can help researchers predict how well a patient recovers from surgery to remove the lower colon, rectum, and bladder, and create openings through which urine and stool are passed out of the body (pelvic exenteration). Comparing the types of surgery completed and procedures used may help researchers to determine which are most effective and safe in patients with a history of gynecologic cancer.
Conditions Studied
Interventions
- OTHER Quality-of-Life Assessment
- OTHER Questionnaire Administration
Study Locations (1)
Texas
- M D Anderson Cancer Center - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 79 participants |
| Start Date | 2008-07-11 |
| Est. Completion | 2027-09-30 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00791635
The ClinicalTrials.gov registry entry for NCT00791635 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 79 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 388-participant average among 27 other Endometrial Carcinoma trials with a reported enrollment target (80% lower). The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.
The record links to 5 conditions, with Endometrial Carcinoma appearing as the primary indexed condition, and to 2 interventions - of which Quality-of-Life Assessment is the first listed.
NCT00791635 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT00791635 about?
NCT00791635 is a clinical study titled "Longitudinal Evaluation of Women Undergoing Pelvic Surgery for the Treatment of Gynecologic Cancer". The study investigates whether certain characteristics of gynecological cancer can help researchers predict how well a patient recovers from surgery to remove the lower colon, rectum, and bladder, and create openings through which urine and stool are passed out of the body (pelvic exenteration). Com...
What is the current status of trial NCT00791635?
This trial is currently active not recruiting. The enrollment target is 79 participants. The study started on 2008-07-11. Estimated completion is 2027-09-30.
What conditions does trial NCT00791635 study?
This clinical trial studies the following conditions: Endometrial Carcinoma, Cervical Carcinoma, Malignant Female Reproductive System Neoplasm, Vulvar Carcinoma, Vaginal Carcinoma.
What interventions are being tested in trial NCT00791635?
The interventions under investigation include: Quality-of-Life Assessment (OTHER), Questionnaire Administration (OTHER).
Who is sponsoring clinical trial NCT00791635?
This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00791635 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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