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NCT00227721 · ClinicalTrials.gov registry record · Phase 2

Gemcitabine and Docetaxel in Treating Patients With Relapsed or Refractory Ovarian Epithelial or Peritoneal Cancer

A Phase 2 study of Ovarian Cancer and Peritoneal Cavity Cancer, sponsored by Robert Morris.

Completed
Registry status
Phase 2
Development phase
30
Enrollment target
4
Study locations

NCT00227721 is a Phase 2 study of Ovarian Cancer and Peritoneal Cavity Cancer that has completed, run by Robert Morris. The registered enrollment target is 30 participants, below the 729-participant average among 322 other Ovarian Cancer trials with a reported enrollment target (96% lower). The trial reports 4 study locations across 3 states.

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The verdict

NCT00227721, a Phase 2 study of Ovarian Cancer and Peritoneal Cavity Cancer, has completed, sponsored by Robert Morris.

COMPLETED
Registry status
Phase 2
Development phase
30 participants
Enrollment target
4
Study locations

Study Summary

RATIONALE: Drugs used in chemotherapy, such as gemcitabine and docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving gemcitabine together with docetaxel works in treating patients with relapsed or refractory ovarian epithelial or peritoneal cancer.

Interventions

  • DRUG Docetaxel
  • DRUG Gemcitabine hydrochloride

Study Locations (4)

Michigan

  • Oakwood Cancer Center at Oakwood Hospital and Medical Center - Dearborn
  • Barbara Ann Karmanos Cancer Institute - Detroit

Ohio

  • Arthur G. James Cancer Hospital and Solove Research Institute at Ohio State University Medical Center - Columbus

Virginia

  • Northern Virginia Pelvic Surgery Assoc - Annandale

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2004-02
Est. Completion 2017-02
Phase Phase 2

Sponsor

Robert Morris

1 total trials

What the Registry Record Tells You About NCT00227721

The ClinicalTrials.gov registry entry for NCT00227721 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 729-participant average among 322 other Ovarian Cancer trials with a reported enrollment target (96% lower). The listed sponsor is Robert Morris, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Ovarian Cancer appearing as the primary indexed condition, and to 2 interventions - of which Docetaxel is the first listed.

NCT00227721 reports 4 study locations spanning 3 distinct geographic areas - top geographies include Michigan, Ohio, Virginia.

Frequently Asked Questions

What is clinical trial NCT00227721 about?

NCT00227721 is a clinical study titled "Gemcitabine and Docetaxel in Treating Patients With Relapsed or Refractory Ovarian Epithelial or Peritoneal Cancer". RATIONALE: Drugs used in chemotherapy, such as gemcitabine and docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. PURPOSE: This phase II t...

What is the current status of trial NCT00227721?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2004-02. Estimated completion is 2017-02.

What conditions does trial NCT00227721 study?

This clinical trial studies the following conditions: Ovarian Cancer, Peritoneal Cavity Cancer.

What interventions are being tested in trial NCT00227721?

The interventions under investigation include: Docetaxel (DRUG), Gemcitabine hydrochloride (DRUG).

Who is sponsoring clinical trial NCT00227721?

This trial is sponsored by Robert Morris, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00227721 being conducted?

This trial has 4 study locations across Michigan, Ohio, Virginia. 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

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.