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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01019330
Other study ID # 09-15552
Secondary ID
Status Completed
Phase N/A
First received November 20, 2009
Last updated November 27, 2015
Start date June 2010
Est. completion date August 2015

Study information

Verified date November 2015
Source Creighton University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Cardiac catheterization has traditionally been performed via access to the arterial circulation from the femoral artery located in the groin. As an alternative to this approach, the radial artery, located in the arm, is gaining wider use in clinical practice. Multiple studies have demonstrated that cardiac catheterization via the radial approach has a very low complication rate, in the short term. This study is intended to determine if there are any differences in the long term complication rate between radial artery cardiac catheterization as compared with femoral artery cardiac catheterization.


Recruitment information / eligibility

Status Completed
Enrollment 243
Est. completion date August 2015
Est. primary completion date August 2015
Accepts healthy volunteers No
Gender Both
Age group 19 Years and older
Eligibility Inclusion Criteria:

- Male or Female

- 19 years old or older

- candidate for radial or femoral cardiac catheterization

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
Allen's test
The Allen's test checks to make sure that radial and ulnar arteries that supply blood to the hand are not blocked. A pulse oximeter is placed on the index finger of the hand. The subject is asked to make a fist for 10 seconds.At this time, pressure is applied over the ulnar and radial arteries as to occlude (block) both of them. The pulse oximeter reading will begin to fall. Radial arterial pressure is then released. If the artery is patent (working), the pulse oximeter reading will begin to rise.
Distal pulses
Practitioner will check that the dorsalis pedis and posterior tibialis are palpable.

Locations

Country Name City State
United States Creighton University Medical Center Omaha Nebraska
United States The Cardiac Center at Creighton University Omaha Nebraska

Sponsors (1)

Lead Sponsor Collaborator
Creighton University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To determine if there is a difference in complication rate measured at 30 days between radial and femoral catheterization 30 days Yes
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