NL-OMON50481
Completed
Not Applicable
A cohort study evaluating upper extremity function after slender transradial percutaneous coronary intervention - Upper extremity dysfunction post slender radial PCI
Amphia Ziekenhuis0 sites100 target enrollmentTBD
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- complaints of hand
- Sponsor
- Amphia Ziekenhuis
- Enrollment
- 100
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- Presenting for elective slender TRPCI using \*5F catheters and a stent on the
- •wire or RX DES Stent at one of the study centres
- •\- 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 clinical condition prohibits or hinders informed consent and/or baseline
- •examinations. E.g. cardiogenic shock and cardiopulmonary resuscitation or
- •subconscious and semiconscious state,
- •\- 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 studied
- •extremities.
- •\- Previous attempts of TRA (transradial approach) were unsuccessful.
Outcomes
Primary Outcomes
Not specified
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