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Preservation of Ovarian Function Via LOT in Squamous Cell Carcinoma of the Cervix

Not Applicable
Terminated
Conditions
Cervical Cancer
Interventions
Procedure: Laparoscopic ovarian transposition
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
Arm && Interventions
GroupInterventionDescription
1Laparoscopic ovarian transpositionLaparoscopic Ovarian Transposition
Primary Outcome Measures
NameTimeMethod
Menopause6 months
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Wisconsin

🇺🇸

Madison, Wisconsin, United States

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