Laparoscopic Sentinel Lymph Node Localization in Operable Cervix Cancer

NCT00205010 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2019-11-19

No results posted yet for this study

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

Conditions

Interventions

PROCEDURE

Lymphoscintigraphy

Sponsors & Collaborators

  • University of Wisconsin, Madison

    lead OTHER

Principal Investigators

  • David M Kushner, MD · University of Wisconsin, Madison

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-10-31
Primary Completion
2006-02-28
Completion
2006-06-30

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00205010 on ClinicalTrials.gov