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NCT00214149 · ClinicalTrials.gov registry record · Phase 2

Multi-catheter High Dose Rate (HDR) Breast Brachytherapy

A Phase 2 study, sponsored by University of Wisconsin, Madison.

Terminated
Registry status
Phase 2
Development phase
127
Enrollment target

NCT00214149: Clinical Trial Phase 2 study, sponsored by University of Wisconsin, Madison.

NCT00214149 is a Phase 2 study that was terminated before completion, run by University of Wisconsin, Madison. The registered enrollment target is 127 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00214149, a Phase 2 study, was terminated before completion, sponsored by University of Wisconsin, Madison.

TERMINATED
Registry status
Phase 2
Development phase
127 participants
Enrollment target

Study Summary

Breast conservation therapy (BCT) is now widely accepted as a treatment option for most women with Stage I and II invasive breast cancer and most patients with ductal carcinoma in situ (DCIS). Despite superior cosmetic outcome, BCT is more complex and requires a protracted treatment regimen comprised of 6 weeks of daily external beam radiation therapy to the whole breast. The purpose of this study is to determine if an acceptable outcome can be achieved with radiation delivered only to the region of the tumor bed. If this is true, partial breast irradiation may lend itself to much shorter treatment times (one week) and the toxicities to adjacent normal structures (heart, lung, chest wall) will be greatly reduced.

Interventions

  • RADIATION brachytherapy

Trial Details

FieldValue
Enrollment Target 127 participants
Start Date 2004-10
Est. Completion 2010-10
Phase Phase 2
University of Wisconsin, Madison

1,039 total trials

Why NCT00214149 stopped before completion

NCT00214149 is an interventional study that assigns participants to a tested intervention. The registered 127 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.

The record links to 0 conditions, and to 1 intervention - of which brachytherapy is the first listed.

NCT00214149 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00214149 about?

NCT00214149 is a clinical study titled "Multi-catheter High Dose Rate (HDR) Breast Brachytherapy". Breast conservation therapy (BCT) is now widely accepted as a treatment option for most women with Stage I and II invasive breast cancer and most patients with ductal carcinoma in situ (DCIS). Despite superior cosmetic outcome, BCT is more complex and requires a protracted treatment regimen comprise...

What is the current status of trial NCT00214149?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 127 participants. The study started on 2004-10. Estimated completion is 2010-10.

What interventions are being tested in trial NCT00214149?

The interventions under investigation include: brachytherapy (RADIATION).

Who is sponsoring clinical trial NCT00214149?

This trial is sponsored by University of Wisconsin, Madison, which has 1,039 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00214149's enrollment target sits among peer trials

127 555th of 2000 higher than 1,445 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 NCT00214149, the US trial registry maintained by the National Library of Medicine. NCT00214149 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.