Actively Recruiting
Association Between Radial Artery Intervention and Development of Neuropathy in the Hand - A Prospective Study - The ACCESS IV Study
Led by Aarhus University Hospital Skejby · Updated on 2026-04-23
400
Participants Needed
1
Research Sites
39 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the possible nerve damage that may occur after radial artery catheterization (CAG) or percutaneous coronary intervention (PCI) in patients with ischemic heart disease. This prospective study aims to assess whether accessing the radial artery increases the risk of nerve injury, particularly affecting the median nerve at the carpal tunnel or the ulnar nerve at Guyon's canal. The study is conducted by Aarhus University Hospital Skejby and focuses on sensory and motor nerve function in the hands. Participants scheduled for radial CAG or PCI will have their sensory and motor nerve functions tested in both wrists and hands before the procedure. The study groups include patients with neurophysiological measurements taken on the same hand as the intervention (ipsilateral) and those measured on the opposite hand (contralateral). Patients will complete questionnaires about hand and arm symptoms, and their ability to perform certain activities will be assessed before and one month after the procedure using tools such as the Katz chart. During the study, participants will undergo neurophysiological nerve measurements lasting about one hour before and one month after the procedure. Researchers will also evaluate the severity of hand symptoms and dysfunction through short questionnaires. This study helps monitor hand function changes over time and aims to identify any increased nerve damage related to radial artery interventions. The total participation involves initial testing, the procedure, and follow-up assessments approximately one month later.
CONDITIONS
Brief Title
Association Between Radial Artery Intervention and Development of Neuropathy in the Hand - A Prospective Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- The patient must be able to give informed consent
You will not qualify if you...
- Pregnancy
- Negative Barbeau test
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 1 day
Participants undergo sensory and motor nerve examinations of both wrists before the radial artery procedure, including questionnaires about hand and arm symptoms and function.
1 visit (in-person)
Duration - 1 day
Participants undergo repeat nerve examinations and complete questionnaires about hand and arm symptoms and function approximately 1 month after the radial artery procedure.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Department of cardiology, Aarhus University Hospital in Skejby
Aarhus, Denmark, 8200
Actively Recruiting
Research Team
C
Christel G Aagren Nielsen
C
Christian J Terkelsen, Professor
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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