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NCT00610740 · ClinicalTrials.gov registry record · Phase 2

CerviPrep for Applying Topical Gemcitabine to the Cervix in Treating Patients With Primary Endometrial, Cervical, or Ovarian Epithelial Cancer

A Phase 2 study of Ovarian Cancer and Endometrial Cancer, sponsored by Masonic Cancer Center, University of Minnesota.

Completed
Registry status
Phase 2
Development phase
18
Enrollment target
1
Study location

NCT00610740 is a Phase 2 study of Ovarian Cancer and Endometrial Cancer that has completed, run by Masonic Cancer Center, University of Minnesota. The registered enrollment target is 18 participants, below the 729-participant average among 322 other Ovarian Cancer trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00610740, a Phase 2 study of Ovarian Cancer and Endometrial Cancer, has completed, sponsored by Masonic Cancer Center, University of Minnesota.

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

Study Summary

RATIONALE: Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Using the CerviPrep™ drug delivery device to apply topical gemcitabine to the cervix may be an effective way to kill more tumor cells. PURPOSE: This phase II trial is studying how well CerviPrep™ works in applying topical gemcitabine to the cervix in treating patients with primary endometrial cancer, cervical cancer, or ovarian epithelial cancer.

Interventions

  • PROCEDURE therapeutic conventional surgery
  • DRUG topical gemcitabine hydrochloride

Study Locations (1)

Minnesota

  • University of Minnesota Cancer Center - Minneapolis

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2006-07
Est. Completion 2008-04
Phase Phase 2

What the Registry Record Tells You About NCT00610740

The ClinicalTrials.gov registry entry for NCT00610740 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 18 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 (98% lower). The listed sponsor is Masonic Cancer Center, University of Minnesota, which has 249 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Ovarian Cancer appearing as the primary indexed condition, and to 2 interventions - of which therapeutic conventional surgery is the first listed.

NCT00610740 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.

Frequently Asked Questions

What is clinical trial NCT00610740 about?

NCT00610740 is a clinical study titled "CerviPrep for Applying Topical Gemcitabine to the Cervix in Treating Patients With Primary Endometrial, Cervical, or Ovarian Epithelial Cancer". RATIONALE: Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Using the CerviPrep™ drug delivery device to apply topical gemcitabine to the cervix may be an effective way to kill mo...

What is the current status of trial NCT00610740?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 18 participants. The study started on 2006-07. Estimated completion is 2008-04.

What conditions does trial NCT00610740 study?

This clinical trial studies the following conditions: Ovarian Cancer, Endometrial Cancer, Cervical Cancer.

What interventions are being tested in trial NCT00610740?

The interventions under investigation include: therapeutic conventional surgery (PROCEDURE), topical gemcitabine hydrochloride (DRUG).

Who is sponsoring clinical trial NCT00610740?

This trial is sponsored by Masonic Cancer Center, University of Minnesota, which has 249 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00610740 being conducted?

This trial has 1 study location across Minnesota. 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.