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Study of Post Operative Pain in Endometrial Cancer Robotic Versus Laparotomy

NCT00909896 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 142

Last updated 2018-04-02

No results posted yet for this study

Summary

This study is being done to evaluate the efficacy of robotic approach for staging of endometrial cancer as compared to an equivalent abdominal approach. The primary objective is to measure and compare postoperative pain at rest at several time points between two groups of patients undergoing either robotic or open laparotomy approach for staging of endometrial cancer.

Conditions

Sponsors & Collaborators

  • Ohio State University Comprehensive Cancer Center

    lead OTHER

Principal Investigators

  • David Cohn, MD · Ohio State University

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-04-08
Primary Completion
2013-01-29
Completion
2013-01-29

Countries

  • United States

Study Locations

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Entities

Diseases

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 NCT00909896 on ClinicalTrials.gov