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NCT00088972 · ClinicalTrials.gov registry record · Phase 2

S0300, Celecoxib in Preventing Breast Cancer in Premenopausal Women

A Phase 2 study, sponsored by SWOG Cancer Research Network.

Terminated
Registry status
Phase 2
Development phase
8
Enrollment target

NCT00088972: Clinical Trial Phase 2 study, sponsored by SWOG Cancer Research Network.

NCT00088972 is a Phase 2 study that was terminated before completion, run by SWOG Cancer Research Network. The registered enrollment target is 8 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00088972, a Phase 2 study, was terminated before completion, sponsored by SWOG Cancer Research Network.

TERMINATED
Registry status
Phase 2
Development phase
8 participants
Enrollment target

Study Summary

RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development or recurrence of cancer. The use of celecoxib may be effective in preventing breast cancer. PURPOSE: This randomized phase II trial is studying how well celecoxib works in preventing breast cancer in premenopausal women who are at risk for developing the disease.

Primary Outcome

The primary outcome measure is change in mammographic density. The null hypothesis is that there is no difference between the arms in change in mammographic density over one year versus the alternative that the treatment arm reduces mammographic density by 10 points (percent of pixels highlighted) or more over one year compared to the change in the placebo arm.

Interventions

  • OTHER placebo
  • DRUG celecoxib

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2004-11
Est. Completion 2009-07
Phase Phase 2
SWOG Cancer Research Network

270 total trials

Why NCT00088972 stopped before completion

NCT00088972 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (94% lower).

The record links to 0 conditions, and to 2 interventions - of which placebo is the first listed.

NCT00088972 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00088972 about?

NCT00088972 is a clinical study titled "S0300, Celecoxib in Preventing Breast Cancer in Premenopausal Women". RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development or recurrence of cancer. The use of celecoxib may be effective in preventing breast cancer. PURPOSE: This randomized phase II trial is studying how well celecoxib works in preventing breast cancer in pr...

What is the current status of trial NCT00088972?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 8 participants. The study started on 2004-11. Estimated completion is 2009-07.

What interventions are being tested in trial NCT00088972?

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

Who is sponsoring clinical trial NCT00088972?

This trial is sponsored by SWOG Cancer Research Network, which has 270 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00088972's enrollment target sits among peer trials

8 1990th of 2000 higher than 5 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00088972, the US trial registry maintained by the National Library of Medicine. NCT00088972 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.