Clinical trial
Study Tests Whether a Standardized LVR Performed With the Blue Egg Device…
NCT00326690 · BioVentrix, Industry · Withdrawn
Key facts
| NCT number | NCT00326690 |
|---|---|
| Title | Study Tests Whether a Standardized LVR Performed With the Blue Egg Device Improves Cardiopulmonary Exercise Capacity |
| Official title | A Prospective, Randomized Trial Using a reproduciBLe volUmE-Measurement stratEGy in the surGical Reconstruction of the Ischemic Cardiomyopathic Heart |
| Lead sponsor | BioVentrix, Industry |
| Status | Withdrawn |
| Study type | Interventional |
| Conditions | Congestive Heart Failure, Ischemic Cardiomyopathy, Coronary Artery Disease, Myocardial Diseases |
| Intervention type | Device |
| Interventions | Blue Egg Device |
| Enrollment | 0 |
| Start date | Nov 1, 2005 |
| Primary completion | Dec 1, 2008 |
| Completion | Dec 1, 2008 |
| First posted | May 17, 2006 |
| Last update posted | Jan 26, 2023 |
| Countries | Germany, United States |
At a glance
- 10–99 Study sites
- No 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: