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Data Collection of Demographics and Perioperative Care of Patients Undergoing Laparoscopic Surgery

M.D. Anderson Cancer Center logo

M.D. Anderson Cancer Center

Status

Terminated

Conditions

Laparoscopy

Treatments

Other: Laparoscopic Surgery Data Collection

Study type

Observational

Funder types

Other

Identifiers

NCT00490126
2006-0170

Details and patient eligibility

About

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.

Full 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.

Enrollment

31 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  1. 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: None

Trial design

31 participants in 1 patient group

Laparoscopic Surgery Database
Treatment:
Other: Laparoscopic Surgery Data Collection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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