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NCT00291694 · ClinicalTrials.gov registry record · Phase 2

Protocol for Women at Increased Risk of Developing Breast Cancer

A Phase 2 study of Breast Cancer, sponsored by Carol Fabian, MD.

Completed
Registry status
Phase 2
Development phase
72
Enrollment target
1
Study location

NCT00291694: Completed Phase 2 study of Breast Cancer, sponsored by Carol Fabian, MD.

NCT00291694 is a Phase 2 study of Breast Cancer that has completed, run by Carol Fabian, MD. The registered enrollment target is 72 participants, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00291694, a Phase 2 study of Breast Cancer, has completed, sponsored by Carol Fabian, MD.

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

Study Summary

To assess the effects of twelve months of celecoxib administration by evaluating breast tissue needle aspirations, to determine if cell growth can be slowed.

Primary Outcome

Immunocytochemical staining of breast epithelial cells. Positive cells reflect proliferative activity.

Conditions Studied

Interventions

  • OTHER placebo
  • DRUG celecoxib

Study Locations (1)

Kansas

  • University of Kansas Medical Center - Kansas City

Trial Details

FieldValue
Enrollment Target 72 participants
Start Date 2003-04
Est. Completion 2009-12
Phase Phase 2
Carol Fabian, MD

14 total trials

What the finished NCT00291694 record still lists

NCT00291694 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 72 participants, a relatively small participant target, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (97% lower).

The record links to 1 condition, with Breast Cancer appearing as the primary indexed condition, and to 2 interventions - of which placebo is the first listed.

NCT00291694 reports a single indexed study location in Kansas.

Frequently Asked Questions

What is clinical trial NCT00291694 about?

NCT00291694 is a clinical study titled "Protocol for Women at Increased Risk of Developing Breast Cancer". To assess the effects of twelve months of celecoxib administration by evaluating breast tissue needle aspirations, to determine if cell growth can be slowed.

What is the current status of trial NCT00291694?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 72 participants. The study started on 2003-04. Estimated completion is 2009-12.

What conditions does trial NCT00291694 study?

This clinical trial studies the following conditions: Breast Cancer.

What interventions are being tested in trial NCT00291694?

The interventions under investigation include: placebo (OTHER), celecoxib (DRUG).

Who is sponsoring clinical trial NCT00291694?

This trial is sponsored by Carol Fabian, MD, which has 14 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00291694 being conducted?

This trial has 1 study location across Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Breast Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00291694's enrollment target sits among peer trials

72 685th of 1224 higher than 533 of 1,224 other Breast Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Breast Cancer trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00291694, the US trial registry maintained by the National Library of Medicine. NCT00291694 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.