Clinical trial
Doppler-Guided Uterine Artery Occlusion (DUAO) Device for Fibroid Related…
NCT00496080 · Ethicon, Inc., Industry · Terminated
Key facts
| NCT number | NCT00496080 |
|---|---|
| Title | Doppler-Guided Uterine Artery Occlusion (DUAO) Device for Fibroid Related Bleeding |
| Official title | A Pivotal Study of Doppler Guided Uterine Artery Occlusion as Treatment for the Reduction of Fibroid Associated Bleeding |
| Acronym | DUAO |
| Lead sponsor | Ethicon, Inc., Industry |
| Status | Terminated |
| Study type | Interventional |
| Conditions | Menorrhagia, Uterine Fibroids |
| Intervention type | Device |
| Interventions | Doppler-Guided Uterine Artery Occlusion Device (DUAO) |
| Enrollment | 87 |
| Start date | Jun 1, 2007 |
| Primary completion | Sep 1, 2010 |
| Completion | Oct 1, 2010 |
| First posted | Jul 4, 2007 |
| Last update posted | Sep 10, 2012 |
| Countries | Canada, Mexico, United States |
At a glance
- 10–99 Study sites
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: