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NCT00064025 · ClinicalTrials.gov registry record · Phase 2

Medroxyprogesterone in Treating Patients With Endometrioid Adenocarcinoma of the Uterine Corpus

A Phase 2 study of Endometrial Adenocarcinoma and Recurrent Uterine Corpus Carcinoma, sponsored by Gynecologic Oncology Group.

Completed
Registry status
Phase 2
Development phase
75
Enrollment target
1
Study location

NCT00064025 is a Phase 2 study of Endometrial Adenocarcinoma and Recurrent Uterine Corpus Carcinoma that has completed, run by Gynecologic Oncology Group. The registered enrollment target is 75 participants, below the 334-participant average among 13 other Endometrial Adenocarcinoma trials with a reported enrollment target (78% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00064025, a Phase 2 study of Endometrial Adenocarcinoma and Recurrent Uterine Corpus Carcinoma, has completed, sponsored by Gynecologic Oncology Group.

COMPLETED
Registry status
Phase 2
Development phase
75 participants
Enrollment target
1
Study location

Study Summary

This phase II trial is studying how well medroxyprogesterone works in treating patients with endometrioid adenocarcinoma (cancer) of the uterine corpus (the body of the uterus, not including the cervix). Hormone therapy using medroxyprogesterone may be effective in treating endometrioid cancer.

Interventions

  • OTHER Laboratory Biomarker Analysis
  • PROCEDURE Therapeutic Conventional Surgery
  • DRUG Medroxyprogesterone

Study Locations (1)

Pennsylvania

  • Gynecologic Oncology Group - Philadelphia

Trial Details

FieldValue
Enrollment Target 75 participants
Start Date 2004-04
Phase Phase 2

Sponsor

Gynecologic Oncology Group

154 total trials

What the Registry Record Tells You About NCT00064025

The ClinicalTrials.gov registry entry for NCT00064025 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 75 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 334-participant average among 13 other Endometrial Adenocarcinoma trials with a reported enrollment target (78% lower). The listed sponsor is Gynecologic Oncology Group, which has 154 total studies on file at ClinicalTrials.gov.

The record links to 8 conditions, with Endometrial Adenocarcinoma appearing as the primary indexed condition, and to 3 interventions - of which Laboratory Biomarker Analysis is the first listed.

NCT00064025 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT00064025 about?

NCT00064025 is a clinical study titled "Medroxyprogesterone in Treating Patients With Endometrioid Adenocarcinoma of the Uterine Corpus". This phase II trial is studying how well medroxyprogesterone works in treating patients with endometrioid adenocarcinoma (cancer) of the uterine corpus (the body of the uterus, not including the cervix). Hormone therapy using medroxyprogesterone may be effective in treating endometrioid cancer.

What is the current status of trial NCT00064025?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 75 participants. The study started on 2004-04.

What conditions does trial NCT00064025 study?

This clinical trial studies the following conditions: Endometrial Adenocarcinoma, Recurrent Uterine Corpus Carcinoma, Stage I Uterine Corpus Cancer, Stage II Uterine Corpus Cancer, Stage III Uterine Corpus Cancer.

What interventions are being tested in trial NCT00064025?

The interventions under investigation include: Laboratory Biomarker Analysis (OTHER), Therapeutic Conventional Surgery (PROCEDURE), Medroxyprogesterone (DRUG).

Who is sponsoring clinical trial NCT00064025?

This trial is sponsored by Gynecologic Oncology Group, which has 154 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00064025 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.