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Trial record 1 of 13 for:    cervical cancer and LOT
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Preservation of Ovarian Function Via LOT in Squamous Cell Carcinoma of the Cervix

This study has been terminated.
(slow accrual)
Sponsor:
ClinicalTrials.gov Identifier:
NCT00204997
First Posted: September 20, 2005
Last Update Posted: October 2, 2015
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.
Information provided by (Responsible Party):
University of Wisconsin, Madison
September 13, 2005
September 20, 2005
October 2, 2015
September 2002
September 2005   (Final data collection date for primary outcome measure)
Menopause [ Time Frame: 6 months ]
Not Provided
Complete list of historical versions of study NCT00204997 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
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Preservation of Ovarian Function Via LOT in Squamous Cell Carcinoma of the Cervix
Preservation of Ovarian Function Via Laparoscopic Transposition in Patients With Locally Advanced Squamous Cell Carcinoma of the Cervix
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
Not Provided
Interventional
Not Provided
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Cervical Cancer
Procedure: Laparoscopic ovarian transposition
Laparoscopic ovarian transposition
Experimental: 1
Laparoscopic Ovarian Transposition
Intervention: Procedure: Laparoscopic ovarian transposition
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
10
February 2008
September 2005   (Final data collection date for primary outcome measure)

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
Sexes Eligible for Study: Female
18 Years to 40 Years   (Adult)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00204997
CO 02702
2002-255
Yes
Not Provided
Not Provided
University of Wisconsin, Madison
University of Wisconsin, Madison
Not Provided
Principal Investigator: David M Kushner, MD University of Wisconsin, Madison
University of Wisconsin, Madison
June 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP