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Completed Phase 2 Interventional

Laparoscopic Staging in Patients With Ovarian, Fallopian Tube, or Other Primary Abdominal Cancers

ClinicalTrials.gov ID: NCT00002538

Public ClinicalTrials.gov record NCT00002538. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 3, 2026, 7:47 PM EST

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

LAPAROSCOPIC STAGING IN PATIENTS WITH INCOMPLETELY STAGED CANCERS OF THE OVARY

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

RATIONALE: Laparoscopic staging may help doctors plan more effective treatment for ovarian, primary fallopian tube, and primary abdominal cancers. PURPOSE: Phase II trial to study the effectiveness of laparoscopic staging in patients with ovarian, primary fallopian tube, or primary abdominal cancers who have not undergone complete staging.

Study identification

NCT ID
NCT00002538
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gynecologic Oncology Group
Network
Enrollment
Not listed

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 1993 (Type not available)
Primary completion
Mar 2010 (Actual)
Completion
Not listed
Last update posted
Aug 20, 2013

Started 1993

United States locations

U.S. sites
11
U.S. states
7
U.S. cities
9
Facility City State ZIP Site status
USC/Norris Comprehensive Cancer Center Los Angeles California 90033-0800 —
Jonsson Comprehensive Cancer Center, UCLA Los Angeles California 90095-1781 —
Women's Cancer Center Palo Alto California 94304 —
Vincent T. Lombardi Cancer Research Center, Georgetown University Washington D.C. District of Columbia 20007 —
Walter Reed Army Medical Center Washington D.C. District of Columbia 20307-5000 —
Rush-Presbyterian-St. Luke's Medical Center Chicago Illinois 60612 —
University of Minnesota Cancer Center Minneapolis Minnesota 55455 —
Duke Comprehensive Cancer Center Durham North Carolina 27710 —
Comprehensive Cancer Center of Wake Forest University Baptist Medical Center Winston-Salem North Carolina 27157-1082 —
University of Oklahoma College of Medicine Oklahoma City Oklahoma 73190 —
Abington Memorial Hospital Abington Pennsylvania 19001 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00002538, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 20, 2013 · Synced Nov 3, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00002538 live on ClinicalTrials.gov.

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