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NCT00774267 · ClinicalTrials.gov registry record

Study Evaluating Changes In Mammographic Breast Density

A clinical trial, sponsored by Pfizer.

Completed
Registry status
507
Enrollment target

NCT00774267: Completed study, sponsored by Pfizer.

NCT00774267 is a clinical trial that has completed, run by Pfizer. The registered enrollment target is 507 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00774267 has completed, sponsored by Pfizer.

COMPLETED
Registry status
507 participants
Enrollment target

Study Summary

The objective of the study is to evaluate quantitative changes in mammographic breast density from baseline to 24 months in postmenopausal women receiving daily doses of either BZA 20 mg/CE 0.45 mg, BZA 20 mg/CE 0.625 mg, Raloxifene or placebo. The primary endpoint in this study is the change in mammographic breast density between baseline and month 24 for each group.

Primary Outcome

The digitized mammogram pairs were analyzed by a single trained radiologist who determined the density of the breast using software. The only left craniocaudal view was used for assessing breast density.

Interventions

  • DRUG Placebo
  • DRUG BZA 20 mg/CE 0.45 mg
  • DRUG BZA 20 mg/CE 0.625 mg
  • DRUG Raloxifene 60 mg

Trial Details

FieldValue
Enrollment Target 507 participants
Start Date 2009-01
Est. Completion 2010-04
Pfizer

1,845 total trials

What the finished NCT00774267 record still lists

NCT00774267 is an observational study that tracks outcomes without assigning an intervention. The registered 507 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.

NCT00774267 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00774267 about?

NCT00774267 is a clinical study titled "Study Evaluating Changes In Mammographic Breast Density". The objective of the study is to evaluate quantitative changes in mammographic breast density from baseline to 24 months in postmenopausal women receiving daily doses of either BZA 20 mg/CE 0.45 mg, BZA 20 mg/CE 0.625 mg, Raloxifene or placebo. The primary endpoint in this study is the change in mam...

What is the current status of trial NCT00774267?

This trial is currently completed. The enrollment target is 507 participants. The study started on 2009-01. Estimated completion is 2010-04.

What interventions are being tested in trial NCT00774267?

The interventions under investigation include: Placebo (DRUG), BZA 20 mg/CE 0.45 mg (DRUG), BZA 20 mg/CE 0.625 mg (DRUG), Raloxifene 60 mg (DRUG).

Who is sponsoring clinical trial NCT00774267?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT00774267, the US trial registry maintained by the National Library of Medicine. NCT00774267 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.