Clinical trial

Medroxyprogesterone in Treating Patients With Endometrioid Adenocarcinoma of the…

NCT00064025 · Gynecologic Oncology Group, Other · Completed

Key facts

NCT number NCT00064025
Title Medroxyprogesterone in Treating Patients With Endometrioid Adenocarcinoma of the Uterine Corpus
Official title A Phase II Pilot Investigation Of The Relationship Of Short Term Depo-Provera (Medroxyprogesterone Acetate) Exposure To The Morphologic , Biochemical, And Molecular Changes In Primary Endometroid Adenocarcinoma of the Uterine Corpus
Lead sponsor Gynecologic Oncology Group, Other
Collaborators National Cancer Institute (NCI) NIH
Status Completed
Phase Phase 2
Study type Interventional
Conditions Endometrial Adenocarcinoma, Endometrial Adenosquamous Carcinoma, Endometrial Endometrioid Adenocarcinoma, Variant With Squamous Differentiation, Recurrent Uterine Corpus Carcinoma, Stage I Uterine Corpus Cancer, Stage II Uterine Corpus Cancer, Stage III Uterine Corpus Cancer, Stage IV Uterine Corpus Cancer
Intervention type Drug, Other, Procedure
Interventions Laboratory Biomarker Analysis, Medroxyprogesterone, Therapeutic Conventional Surgery
Enrollment 75
Start date Apr 1, 2004
Primary completion Sep 1, 2010
First posted Jul 9, 2003
Last update posted Apr 11, 2016
Countries United States

At a glance

  • 1–9 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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