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Clinical Trials/NCT00490126
NCT00490126
Terminated
N/A

Data Collection of Demographics and Perioperative Care of Patients Undergoing Laparoscopic Surgery in the Department of Gynecologic Oncology

M.D. Anderson Cancer Center1 site in 1 country31 target enrollmentJune 15, 2006
ConditionsLaparoscopy

Overview

Phase
N/A
Intervention
Not specified
Conditions
Laparoscopy
Sponsor
M.D. Anderson Cancer Center
Enrollment
31
Locations
1
Primary Endpoint
Collect, both prospectively and retrospectively, data on demographics, perioperative care, and patient outcomes in patients undergoing laparoscopic surgery.
Status
Terminated
Last Updated
7 years ago

Overview

Brief Summary

The goal of this clinical research study is to collect information on patients who had or are going to have laparoscopy performed at M. D. Anderson. Researchers want to use this information to learn the effects of laparoscopic surgery on patients over time.

Detailed Description

If you agree to take part in this study, your demographic information (such as your age, race, medical and surgical history, and type of cancer) will be collected. Information about the type of surgical procedure performed on you, your care during and after your surgery, any problems related to your surgery, and details about your follow-up care will be entered into a research database. This information will be collected from patients seen at M. D. Anderson since January 1, 1990. It will be used for future research studies. The research database will be updated, after about 1 year, to include information on your disease outcome, treatment, and/or follow-up care. This information will be collected from your medical record, if possible. If it is not in your medical record, you may again be contacted so that researchers can learn this information. Your participation in this study will continue up to 5 years after your laparoscopic procedure. This is an investigational study. Up to 1,000 patients will take part in this study. All will be enrolled at M. D. Anderson.

Registry
clinicaltrials.gov
Start Date
June 15, 2006
End Date
September 18, 2018
Last Updated
7 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All patients who had or will have laparoscopic surgery in the Department of Gynecologic Oncology (Gynecologic Oncology and General Gynecology) since January 1, 1990 forward.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Collect, both prospectively and retrospectively, data on demographics, perioperative care, and patient outcomes in patients undergoing laparoscopic surgery.

Time Frame: 21 Years

Secondary Outcomes

  • Organize clinical information, patient characteristics, treatment, and laparoscopic outcome data into a single data repository, maintained in a secure platform that will provide an archive for future research.(21 Years)

Study Sites (1)

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