Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00399321 · ClinicalTrials.gov registry record

A Pilot Study of Bone Mineral Density in Postmenopausal Women After Treatment for Breast Cancer

A clinical trial of Breast Cancer and Postmenopausal Bone Loss, sponsored by University of Michigan Rogel Cancer Center.

Completed
Registry status
9
Enrollment target
1
Study location

NCT00399321: Completed study of Breast Cancer and Postmenopausal Bone Loss, sponsored by University of Michigan Rogel Cancer Center.

NCT00399321 is a study of Breast Cancer and Postmenopausal Bone Loss that has completed, run by University of Michigan Rogel Cancer Center. The registered enrollment target is 9 participants, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00399321, a study of Breast Cancer and Postmenopausal Bone Loss, has completed, sponsored by University of Michigan Rogel Cancer Center.

COMPLETED
Registry status
9 participants
Enrollment target
1
Study location

Study Summary

The main purpose of this study is to see what levels of Bone Mineral Density post-menopausal women with breast cancer have, and to see if the level of Bone Mineral Density changes during a women's treatment after her surgery. This trial studies changes in Bone Mineral Density and markers of of bone activity in post-menopausal women receiving treatment for early stage breast cancer.

Study Locations (1)

Michigan

  • University of Michigan Comprehensive Cancer Center - Ann Arbor

Trial Details

FieldValue
Enrollment Target 9 participants
Start Date 2006-04
Est. Completion 2010-09

What the finished NCT00399321 record still lists

NCT00399321 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 9 participants, a relatively small participant target, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (100% lower).

The record links to 2 conditions, with Breast Cancer appearing as the primary indexed condition, and to 0 interventions.

NCT00399321 reports a single indexed study location in Michigan.

Frequently Asked Questions

What is clinical trial NCT00399321 about?

NCT00399321 is a clinical study titled "A Pilot Study of Bone Mineral Density in Postmenopausal Women After Treatment for Breast Cancer". The main purpose of this study is to see what levels of Bone Mineral Density post-menopausal women with breast cancer have, and to see if the level of Bone Mineral Density changes during a women's treatment after her surgery. This trial studies changes in Bone Mineral Density and markers of of bone...

What is the current status of trial NCT00399321?

This trial is currently completed. The enrollment target is 9 participants. The study started on 2006-04. Estimated completion is 2010-09.

What conditions does trial NCT00399321 study?

This clinical trial studies the following conditions: Breast Cancer, Postmenopausal Bone Loss.

Who is sponsoring clinical trial NCT00399321?

This trial is sponsored by University of Michigan Rogel Cancer Center, which has 292 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00399321 being conducted?

This trial has 1 study location across Michigan. 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 NCT00399321's enrollment target sits among peer trials

9 1190th of 1224 higher than 30 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00399321, the US trial registry maintained by the National Library of Medicine. NCT00399321 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.