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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00204997
Other study ID # CO02702
Secondary ID 2002-255A532820S
Status Terminated
Phase N/A
First received
Last updated
Start date September 2002
Est. completion date February 2008

Study information

Verified date June 2008
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


Recruitment information / eligibility

Status Terminated
Enrollment 10
Est. completion date February 2008
Est. primary completion date September 2005
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility 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


Intervention

Procedure:
Laparoscopic ovarian transposition
Laparoscopic ovarian transposition

Locations

Country Name City State
United States University of Wisconsin Madison Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Menopause 6 months
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