Trials / Completed
CompletedNCT01001663
Comparison of the FemoSeal® Arterial Closure Device to Manual Compression After Coronary Angiography
Comparison of the FemoSeal® Arterial Closure Device to Manual Compression After Coronary Angiography: the CLOSE-UP I Randomized Trial
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 1,005 (actual)
- Sponsor
- Aarhus University Hospital Skejby · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Is the FemoSeal® closure device safer and more comfortable than manual compression for femoral artery access closure after coronary angiography?
Detailed description
Access site complication after coronary angiography is still a challenge in everyday practice. The FemoSeal® closure device has proven very safe as shown in the swedish SCAAR registry. This study is aimed to investigate, in a randomized design, if the FemoSeal® has an advantage in safety and efficacy over manual compression.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | FemoSeal® | Closure device for femoral artery access closure |
| OTHER | Manual compression | Conventional manual compression |
Timeline
- Start date
- 2009-09-01
- Primary completion
- 2010-09-01
- Completion
- 2010-09-01
- First posted
- 2009-10-26
- Last updated
- 2026-01-02
Locations
1 site across 1 country: Denmark
Source: ClinicalTrials.gov record NCT01001663. Inclusion in this directory is not an endorsement.