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NCT00545792 · ClinicalTrials.gov registry record · Phase 2

Safety Study Of Avastin And Pelvic Radiation In Women With Recurrent Gynecological Cancers

A Phase 2 study of Ovarian Cancer and Endometrial Cancer, sponsored by Dana-Farber Cancer Institute.

Completed
Registry status
Phase 2
Development phase
21
Enrollment target
1
Study location

NCT00545792 is a Phase 2 study of Ovarian Cancer and Endometrial Cancer that has completed, run by Dana-Farber Cancer Institute. The registered enrollment target is 21 participants, below the 729-participant average among 322 other Ovarian Cancer trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00545792, a Phase 2 study of Ovarian Cancer and Endometrial Cancer, has completed, sponsored by Dana-Farber Cancer Institute.

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

Study Summary

This research study is evaluating a drug called avastin in combination with standard radiation as a possible treatment for treatment for recurrent pelvic-confined gynecological cancer (i.e. endometrial, cervical, vulvar, ovarian or vaginal cancers).

Interventions

  • DRUG Avastin

Study Locations (1)

Massachusetts

  • Dana-Farber Cancer Institute - Boston

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2007-05
Est. Completion 2013-10
Phase Phase 2

Sponsor

Dana-Farber Cancer Institute

781 total trials

What the Registry Record Tells You About NCT00545792

The ClinicalTrials.gov registry entry for NCT00545792 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 21 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 (97% lower). The listed sponsor is Dana-Farber Cancer Institute, which has 781 total studies on file at ClinicalTrials.gov.

The record links to 5 conditions, with Ovarian Cancer appearing as the primary indexed condition, and to 1 intervention - of which Avastin is the first listed.

NCT00545792 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT00545792 about?

NCT00545792 is a clinical study titled "Safety Study Of Avastin And Pelvic Radiation In Women With Recurrent Gynecological Cancers". This research study is evaluating a drug called avastin in combination with standard radiation as a possible treatment for treatment for recurrent pelvic-confined gynecological cancer (i.e. endometrial, cervical, vulvar, ovarian or vaginal cancers).

What is the current status of trial NCT00545792?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 21 participants. The study started on 2007-05. Estimated completion is 2013-10.

What conditions does trial NCT00545792 study?

This clinical trial studies the following conditions: Ovarian Cancer, Endometrial Cancer, Cervical Cancer, Vaginal Cancer, Carcinoma of the Vulva.

What interventions are being tested in trial NCT00545792?

The interventions under investigation include: Avastin (DRUG).

Who is sponsoring clinical trial NCT00545792?

This trial is sponsored by Dana-Farber Cancer Institute, which has 781 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00545792 being conducted?

This trial has 1 study location across Massachusetts. 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.