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NCT00882089 · ClinicalTrials.gov registry record · Phase 4
Use of the Contura™ Catheter in Intermediate-Risk, Pathological Stage 0, I, or II (Up to 3.0 cm) Breast Cancer Patients
A Phase 4 study, sponsored by Cancer Center of Irvine.
- Completed
- Registry status
- Phase 4
- Development phase
- 13
- Enrollment target
NCT00882089: Completed Phase 4 study, sponsored by Cancer Center of Irvine.
NCT00882089 is a Phase 4 study that has completed, run by Cancer Center of Irvine. The registered enrollment target is 13 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00882089, a Phase 4 study, has completed, sponsored by Cancer Center of Irvine.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 13 participants
- Enrollment target
Study Summary
The purpose of this study is to determine if a Contura catheter can avoid a radiation "hot spot" in the skin and improve tissue-balloon conformance in early-stage breast cancer patients undergoing accelerated partial breast irradiation.
Interventions
- DEVICE Contura catheter
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 13 participants |
| Start Date | 2007-10 |
| Est. Completion | 2009-12 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00882089
The ClinicalTrials.gov registry entry for NCT00882089 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 13 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cancer Center of Irvine, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Contura catheter is the first listed.
NCT00882089 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00882089 about?
NCT00882089 is a clinical study titled "Use of the Contura™ Catheter in Intermediate-Risk, Pathological Stage 0, I, or II (Up to 3.0 cm) Breast Cancer Patients". The purpose of this study is to determine if a Contura catheter can avoid a radiation "hot spot" in the skin and improve tissue-balloon conformance in early-stage breast cancer patients undergoing accelerated partial breast irradiation.
What is the current status of trial NCT00882089?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 13 participants. The study started on 2007-10. Estimated completion is 2009-12.
What interventions are being tested in trial NCT00882089?
The interventions under investigation include: Contura catheter (DEVICE).
Who is sponsoring clinical trial NCT00882089?
This trial is sponsored by Cancer Center of Irvine, which has 3 total clinical trials registered on ClinicalTrials.gov.
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Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.