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Clinical Trials/NL-OMON50481
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

Sponsor
Amphia Ziekenhuis

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