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NCT00998023 · ClinicalTrials.gov registry record · NA
Patient Comfort With Vascular Closure
A NA study, sponsored by University of Florida.
- Completed
- Registry status
- NA
- Development phase
- 64
- Enrollment target
NCT00998023: Completed NA study, sponsored by University of Florida.
NCT00998023 is a NA study that has completed, run by University of Florida. The registered enrollment target is 64 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00998023, a NA study, has completed, sponsored by University of Florida.
- COMPLETED
- Registry status
- NA
- Development phase
- 64 participants
- Enrollment target
Study Summary
The purpose of this research study is to collect information on the amount of discomfort patients experience with one of two different vascular blood vessel closure devices, the MynxM5 Vascular Closure Device and the Angio-Seal Evolution Vascular Closure Device.
Primary Outcome
The Visual Analogue Scale measures the severity of pain on a continuous scale from 0 (no pain) to 10 (worst possible pain).
Interventions
- DEVICE Mynx Vascular Closure Device
- DEVICE AngioSeal Vascular Closure Device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 64 participants |
| Start Date | 2009-10 |
| Est. Completion | 2010-08 |
| Phase | NA |
What the finished NCT00998023 record still lists
NCT00998023 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).
The record links to 0 conditions, and to 2 interventions - of which Mynx Vascular Closure Device is the first listed.
NCT00998023 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00998023 about?
NCT00998023 is a clinical study titled "Patient Comfort With Vascular Closure". The purpose of this research study is to collect information on the amount of discomfort patients experience with one of two different vascular blood vessel closure devices, the MynxM5 Vascular Closure Device and the Angio-Seal Evolution Vascular Closure Device.
What is the current status of trial NCT00998023?
This trial is currently completed. It is a NA study. The enrollment target is 64 participants. The study started on 2009-10. Estimated completion is 2010-08.
What interventions are being tested in trial NCT00998023?
The interventions under investigation include: Mynx Vascular Closure Device (DEVICE), AngioSeal Vascular Closure Device (DEVICE).
Who is sponsoring clinical trial NCT00998023?
This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00998023's enrollment target sits among peer trials
64 1147th of 2000 higher than 844 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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