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NCT00081263 · ClinicalTrials.gov registry record · Phase 2

Celecoxib in Treating Patients With Cervical Intraepithelial Neoplasia

A Phase 2 study of Cervical Carcinoma and Stage 0 Cervical Cancer, sponsored by Gynecologic Oncology Group.

Completed
Registry status
Phase 2
Development phase
130
Enrollment target
20
Study locations

NCT00081263 is a Phase 2 study of Cervical Carcinoma and Stage 0 Cervical Cancer that has completed, run by Gynecologic Oncology Group. The registered enrollment target is 130 participants, below the 530-participant average among 25 other Cervical Carcinoma trials with a reported enrollment target (75% lower). The trial reports 20 study locations across 7 states.

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The verdict

NCT00081263, a Phase 2 study of Cervical Carcinoma and Stage 0 Cervical Cancer, has completed, sponsored by Gynecologic Oncology Group.

COMPLETED
Registry status
Phase 2
Development phase
130 participants
Enrollment target
20
Study locations

Study Summary

This randomized phase II trial studies how well celecoxib works in treating patients with cervical intraepithelial neoplasia, a precancerous lesion of the cervix which can develop into cervical cancer. Celecoxib may be effective in preventing the development of cervical cancer in patients who have cervical intraepithelial neoplasia.

Interventions

  • OTHER Placebo
  • OTHER Laboratory Biomarker Analysis
  • DRUG Celecoxib

Study Locations (20)

Indiana

  • Elkhart Clinic - Elkhart
  • Michiana Hematology Oncology PC-Elkhart - Elkhart
  • Elkhart General Hospital - Elkhart
  • Community Howard Regional Health - Kokomo
  • IU Health La Porte Hospital - La Porte
  • Michiana Hematology Oncology PC-Mishawaka - Mishawaka
  • Saint Joseph Regional Medical Center-Mishawaka - Mishawaka
  • Michiana Hematology Oncology PC-Plymouth - Plymouth
  • Memorial Hospital of South Bend - South Bend
  • Michiana Hematology Oncology PC-South Bend - South Bend
  • Northern Indiana Cancer Research Consortium - South Bend
  • Michiana Hematology Oncology PC-Westville - Westville

Delaware

  • Beebe Medical Center - Lewes
  • Christiana Care Health System-Christiana Hospital - Newark

Michigan

  • Borgess Medical Center - Kalamazoo
  • Bronson Methodist Hospital - Kalamazoo

Arizona

  • University of Arizona Cancer Center-North Campus - Tucson

Arkansas

  • University of Arkansas for Medical Sciences - Little Rock

Illinois

  • Carle Clinic-Urbana Main - Urbana

Maryland

  • Union Hospital of Cecil County - Elkton

Trial Details

FieldValue
Enrollment Target 130 participants
Start Date 2005-06
Phase Phase 2

Sponsor

Gynecologic Oncology Group

154 total trials

What the Registry Record Tells You About NCT00081263

The ClinicalTrials.gov registry entry for NCT00081263 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 130 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 530-participant average among 25 other Cervical Carcinoma trials with a reported enrollment target (75% lower). The listed sponsor is Gynecologic Oncology Group, which has 154 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Cervical Carcinoma appearing as the primary indexed condition, and to 3 interventions - of which Placebo is the first listed.

NCT00081263 reports 20 study locations spanning 7 distinct geographic areas - top geographies include Indiana, Delaware, Michigan.

Frequently Asked Questions

What is clinical trial NCT00081263 about?

NCT00081263 is a clinical study titled "Celecoxib in Treating Patients With Cervical Intraepithelial Neoplasia". This randomized phase II trial studies how well celecoxib works in treating patients with cervical intraepithelial neoplasia, a precancerous lesion of the cervix which can develop into cervical cancer. Celecoxib may be effective in preventing the development of cervical cancer in patients who have c...

What is the current status of trial NCT00081263?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 130 participants. The study started on 2005-06.

What conditions does trial NCT00081263 study?

This clinical trial studies the following conditions: Cervical Carcinoma, Stage 0 Cervical Cancer, Cervical Intraepithelial Neoplasia Grade 2/3.

What interventions are being tested in trial NCT00081263?

The interventions under investigation include: Placebo (OTHER), Laboratory Biomarker Analysis (OTHER), Celecoxib (DRUG).

Who is sponsoring clinical trial NCT00081263?

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

Where is trial NCT00081263 being conducted?

This trial has 20 study locations across Arizona, Arkansas, Delaware, Illinois, Indiana. 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.