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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT02583854 |
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Date of registration:
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21/10/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Comparison Study of Compression Devices Used in Transradial Coronary Angiography
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Scientific title:
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Date of first enrolment:
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September 2015 |
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Target sample size:
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499 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02583854 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Supportive Care. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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Norway
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients undergoing coronary angiograms via the transradial route
Exclusion Criteria:
- Patients who have a long way to travel for the follow up, ultrasound scan
- Patients that do not understand Norwegian
- Patients presenting with acute ST segment elevation myocardial infarction (STEMI)
Age minimum:
N/A
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Hemostasis
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Peripheral Artery Occlusion
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Injury of Radial Artery
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Intervention(s)
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Device: RY-STOP hemostasis device
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Device: TR-Band, Terumo
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Primary Outcome(s)
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Radial artery occlusion
[Time Frame: 90-120 days]
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Secondary Outcome(s)
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Patient experience
[Time Frame: 1-4 hours]
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Device complications
[Time Frame: 1-4 hours]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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