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NCT00023621 · ClinicalTrials.gov registry record · Phase 2

Celecoxib in Preventing Basal Cell Carcinoma in Patients With Basal Cell Nevus Syndrome

A Phase 2 study of Non-melanomatous Skin Cancer, sponsored by University of California, San Francisco.

Completed
Registry status
Phase 2
Development phase
60
Enrollment target
2
Study locations

NCT00023621 is a Phase 2 study of Non-melanomatous Skin Cancer that has completed, run by University of California, San Francisco. The registered enrollment target is 60 participants. The trial reports 2 study locations across 2 states.

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The verdict

NCT00023621, a Phase 2 study of Non-melanomatous Skin Cancer, has completed, sponsored by University of California, San Francisco.

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

Study Summary

RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development of cancer. The use of celecoxib may be an effective way to prevent the development of basal cell carcinoma. PURPOSE: Randomized phase II trial to determine the effectiveness of celecoxib in preventing basal cell carcinoma in patients who have basal cell nevus syndrome.

Interventions

  • DRUG celecoxib

Study Locations (2)

California

  • UCSF Comprehensive Cancer Center - San Francisco

New York

  • Herbert Irving Comprehensive Cancer Center at Columbia University Medical Center - New York

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2001-02
Est. Completion 2007-07
Phase Phase 2

What the Registry Record Tells You About NCT00023621

The ClinicalTrials.gov registry entry for NCT00023621 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Non-melanomatous Skin Cancer appearing as the primary indexed condition, and to 1 intervention - of which celecoxib is the first listed.

NCT00023621 reports 2 study locations spanning 2 distinct geographic areas - top geographies include California, New York.

Frequently Asked Questions

What is clinical trial NCT00023621 about?

NCT00023621 is a clinical study titled "Celecoxib in Preventing Basal Cell Carcinoma in Patients With Basal Cell Nevus Syndrome". RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development of cancer. The use of celecoxib may be an effective way to prevent the development of basal cell carcinoma. PURPOSE: Randomized phase II trial to determine the effectiveness of celecoxib in preventing b...

What is the current status of trial NCT00023621?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 60 participants. The study started on 2001-02. Estimated completion is 2007-07.

What conditions does trial NCT00023621 study?

This clinical trial studies the following conditions: Non-melanomatous Skin Cancer.

What interventions are being tested in trial NCT00023621?

The interventions under investigation include: celecoxib (DRUG).

Who is sponsoring clinical trial NCT00023621?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00023621 being conducted?

This trial has 2 study locations across California, New York. 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.