NL-OMON50481CompletedNot 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 enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 100
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18 to 99 (—)
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.
Investigators
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