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NCT00222430 · ClinicalTrials.gov registry record · NA
Fluoroscopy Guided Femoral Arterial Access
A NA study, sponsored by University of Oklahoma.
- Completed
- Registry status
- NA
- Development phase
- 990
- Enrollment target
NCT00222430 is a NA study that has completed, run by University of Oklahoma. The registered enrollment target is 990 participants.
The verdict
NCT00222430, a NA study, has completed, sponsored by University of Oklahoma.
- COMPLETED
- Registry status
- NA
- Development phase
- 990 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the use of fluoroscopic guidance, (a commonly used X-ray technique), with the traditional approach, (where the doctors feel for the strongest pulse), to obtain access to the blood vessel in the groin. These two methods are being compared to assess which is faster, safer and more often allows your physician to use an "arterial closure device," a small suture or plug applied at the end of the angiogram where the needle enters your blood vessel if he/she chooses.
Interventions
- PROCEDURE Fluoroscopy
- PROCEDURE Active Comparator
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 990 participants |
| Start Date | 2005-03 |
| Est. Completion | 2006-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00222430
The ClinicalTrials.gov registry entry for NCT00222430 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 990 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Oklahoma, which has 358 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Fluoroscopy is the first listed.
NCT00222430 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00222430 about?
NCT00222430 is a clinical study titled "Fluoroscopy Guided Femoral Arterial Access". The purpose of this study is to compare the use of fluoroscopic guidance, (a commonly used X-ray technique), with the traditional approach, (where the doctors feel for the strongest pulse), to obtain access to the blood vessel in the groin. These two methods are being compared to assess which is fas...
What is the current status of trial NCT00222430?
This trial is currently completed. It is a NA study. The enrollment target is 990 participants. The study started on 2005-03. Estimated completion is 2006-07.
What interventions are being tested in trial NCT00222430?
The interventions under investigation include: Fluoroscopy (PROCEDURE), Active Comparator (PROCEDURE).
Who is sponsoring clinical trial NCT00222430?
This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.
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