A cohort study evaluating upper extremity dysfunction after percutaneous coronary intervention using the radial artery as access route

Completed

• Conditions: complaints of hand; upper extremity dysfunction; wrist and arm; 10011082; 10023213; 10034606

• Registration Number: NL-OMON38780
• Lead Sponsor: Albert Schweitzer Ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 11 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 490

Inclusion Criteria

-Presenting for TransRadial Percutaneous Coronary Intervention (TR-PCI) at the study centre.
-The radial artery can be palpated and Doppler ultrasound examination of the radial artery shows non-occlusive flow.

Exclusion Criteria

-Currently enrolled in another study that clinically interferes with the current study and that has not passed the primary endpoint.
-The presenting condition prohibits or hinders informed consent and/or baseline examinations, such as a subconscious or semiconscious state, cardiogenic shock or cardiopulmonary resuscitation.
-Co-morbid condition(s) that could limit the subject*s ability to participate in the study or to comply with follow-up requirements, or impact the scientific integrity of the study, e.g. loss of voluntary motor control of the studies extremities

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified