Radical Trachelectomy for Women With Early Stage Cervical Cancer
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00813007|
Recruitment Status : Active, not recruiting
First Posted : December 22, 2008
Last Update Posted : October 20, 2017
The goal of this research study is to learn about quality of life, sexual functioning, and symptoms in women who have undergone abdominal radical trachelectomy for cervical cancer.
This is an investigational study.
Up to 100 patients will be enrolled in this study. All will be enrolled at MD Anderson.
|Condition or disease||Intervention/treatment|
|Cervical Cancer||Behavioral: Questionnaires|
Show Detailed Description
|Study Type :||Observational|
|Actual Enrollment :||50 participants|
|Official Title:||Radical Trachelectomy for Women With Early Stage Cervical Cancer|
|Actual Study Start Date :||December 16, 2008|
|Estimated Primary Completion Date :||December 2019|
|Estimated Study Completion Date :||December 2019|
Radical trachelectomy outcomes for cervical cancer
5 Questionnaires at differing times before and after surgery.
Other Name: Survey
- Mean scores for the General Health-Related Quality of Life (SF-12) [ Time Frame: Follow up visits annually ]Completed SF-12 questionnaires at baseline and at each follow-up visit (4-6 weeks, 6 months, 1 year, and annually for 4 more years)
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00813007
|United States, Texas|
|University of Texas MD Anderson Cancer Center|
|Houston, Texas, United States, 77030|
|Principal Investigator:||Michael M. Frumovitz, MD||M.D. Anderson Cancer Center|