Gynecologic Cancer Lymphedema Questionnaire as a Clinical Care Tool to Identify Lower Extremity Lymphedema
Completed
Conditions studied: Ovarian Cancer, Uterine Cancer, Vaginal Cancer, Lymphedema
In brief
The purpose of this study is to evaluate if the Gynecologic Cancer Lymphedema Questionnaire (GCLQ) truly detects symptoms or signs of lower extremity lymphedema in patients with diagnosed lower extremity lymphedema. Lymphedema is a chronic condition in which fluid accumulates in the tissues of the body. Many cancer survivors are living with discomfort and changes in their activities due to limb swelling following cancer treatment. If the GCLQ is able to do detect signs and symptoms of lymphedema, the investigators hope to use it as a tool in the clinical care setting to help identify women at risk for or with lymphedema. In the future, this could improve clinical care through the use of a more simple and feasible way to identify lower extremity lymphedema than measuring limbs.
Key facts
- Study ID
- NCT00944944
- Run by
- Memorial Sloan Kettering Cancer Center
- People needed
- 58
- Starts
- 2009-07-01
- Expected to finish
- 2010-01-01
- Last updated by the study team
- 2010-02-01
Who can join
Age: 21 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Study group of Gynecologic cancer survivors with Lymphedema
- Documented lower extremity lymphedema
- History of a primary diagnosis of gynecologic cancer (vulvar, cervical and uterine only)
- History of surgery for gynecologic cancer including lymph node removal
- No evidence of disease or active treatment
- At least 21 years of age
- Able and willing to provide informed consent
- English fluency Comparison Group of Gynecologic Cancer Survivors without Lymphedema
- No history of lower extremity lymphedema or presence of lymphedema confirmed by limb volume measurements at the time of study participation
- History of a primary diagnosis of gynecologic cancer (vulvar, cervical and uterine only)
- History of surgery for gynecologic cancer including lymph node removal
- No evidence of disease or active treatment
- At least 21 years of age
- Able and willing to provide informed consent
- English fluency
You may not qualify if…
- Inability to participate in an informed consent process
- Patients with a psychiatric disorder precluding response to the survey
Where it is running
- Memorial Sloan Kettering Cancer Center — New York, New York, United States
Full record on ClinicalTrials.gov
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