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Completed Phase 2 Interventional Results available

Gemcitabine in Treating Patients With Recurrent or Persistent Endometrial Cancer

ClinicalTrials.gov ID: NCT00820898

Public ClinicalTrials.gov record NCT00820898. 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 Jul 21, 2026, 4:17 AM EDT

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

Official title

A Phase II Evaluation of Gemcitabine (Gemzar®, LY188011) in the Treatment of Recurrent or Persistent Endometrial Carcinoma

Study identification

NCT ID
NCT00820898
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gynecologic Oncology Group
Network
Enrollment
24 participants

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
Jan 31, 2009
Primary completion
Dec 31, 2010
Completion
Not listed
Last update posted
Dec 28, 2017

Started 2009

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
Hartford Hospital Hartford Connecticut 06102
Rush University Medical Center Chicago Illinois 60612
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637
Decatur Memorial Hospital Decatur Illinois 62526
Memorial Medical Center Springfield Illinois 62781-0001
Saint Vincent Hospital and Health Services Indianapolis Indiana 46260
University of Iowa/Holden Comprehensive Cancer Center Iowa City Iowa 52242
Maine Medical Center-Bramhall Campus Portland Maine 04102
Cooper Hospital University Medical Center Camden New Jersey 08103
Carolinas Medical Center Charlotte North Carolina 28203
MetroHealth Medical Center Cleveland Ohio 44109
Riverside Methodist Hospital Columbus Ohio 43214
Lake University Ireland Cancer Center Mentor Ohio 44060
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104
Tulsa Cancer Institute Tulsa Oklahoma 74146
Abington Memorial Hospital Abington Pennsylvania 19001
Gynecologic Oncology Group Philadelphia Pennsylvania 19103
Women and Infants Hospital Providence Rhode Island 02905
Zale Lipshy University Hospital Dallas Texas 75235
University of Wisconsin Hospital and Clinics Madison Wisconsin 53792

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 NCT00820898, 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 Dec 28, 2017 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00820898 live on ClinicalTrials.gov.

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