Preservation of Ovarian Function Via LOT in Squamous Cell Carcinoma of the Cervix
Not Applicable
Terminated
- Conditions
- Cervical Cancer
- Registration Number
- NCT00204997
- Lead Sponsor
- University of Wisconsin, Madison
- Brief Summary
The purpose of this study is to evaluate the feasibility, safety and efficacy of laparoscopic ovarian transposition in women less than 40 years of age with locally advanced cervical squamous cell carcinoma
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- Female
- Target Recruitment
- 10
Inclusion Criteria
- Newly diagnosed Stages iB-iiiB squamous cell carcinoma of the cervix
Exclusion Criteria
- Evidence of ovarian involvement on MRI
- Evidence of uterine involvement on MRI
- Evidence of distant mets on MRI
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Menopause 6 months
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie ovarian function preservation after laparoscopic transposition in cervical cancer patients?
How does laparoscopic ovarian transposition compare to standard fertility preservation methods in cervical cancer management?
What biomarkers are associated with successful ovarian function preservation in locally advanced cervical squamous cell carcinoma?
What are the long-term adverse events associated with laparoscopic ovarian transposition in young cervical cancer patients?
Are there combination therapies or alternative approaches to preserving ovarian function in cervical cancer treatment?
Trial Locations
- Locations (1)
University of Wisconsin
🇺🇸Madison, Wisconsin, United States
University of Wisconsin🇺🇸Madison, Wisconsin, United States