Groin Complications Post Percutaneous Coronary Intervention Using Either Manual Compression or PERCLOSE Device
Femoral Access Site Groin Complication Rates After 2517 Groin Punctures Undergoing Vascular Closure by Either Manual Compression or the Perclose Vascular Closure Device
Sponsor: Abbott Medical Devices
A observational or N/A phase clinical study on Vascular Closure, this trial is completed. The trial is conducted by Abbott Medical Devices and has accumulated 7 data snapshots since 2008. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
7 versions recorded-
Sep 2024 — Present [monthly]
Completed
-
Jul 2024 — Sep 2024 [monthly]
Completed
-
Jan 2021 — Jul 2024 [monthly]
Completed
-
Dec 2018 — Jan 2021 [monthly]
Completed
-
Jun 2018 — Dec 2018 [monthly]
Completed
▶ Show 2 earlier versions
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Apr 2018 — Jun 2018 [monthly]
Completed
Phase: NA → None
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Jan 2017 — Apr 2018 [monthly]
Completed NA
First recorded
Jun 2008
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Abbott Medical Devices
- Clinyx, LLC
For direct contact, visit the study record on ClinicalTrials.gov .