An interventional study of Standardized compressive dressing and Hemostasis with TerumoBand® in Coronary Artery Disease With Myocardial Infarction, sponsored by Hospital de Clinicas de Porto Alegre. Completed at 1 site in Brazil. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2020-08-12.
Sponsored by Hospital de Clinicas de Porto Alegre · Not applicable, Interventional, and Treatment
Randomized clinical trial to compare radial artery patency after transradial coronary catheterization using 2 different hemostasis techniques. Patients submitted to diagnostic or therapeutic coronary catheterization will be prospectively enrolled in this single-center trial and will be randomized to radial hemostasis with TerumoBand® or a standardized compressive dressing with gauze and elastic bandage.
Randomized clinical trial to compare radial artery patency after transradial coronary catheterization using 2 different hemostasis techniques. Patients submitted to diagnostic or therapeutic coronary catheterization will be prospectively enrolled in this single-center trial and will be randomized to radial hemostasis with TerumoBand® or a standardized compressive dressing with gauze and elastic bandage.
Interventions: Radial hemostasis with TerumoBand® and Radial hemostasis with a standardized compressive dressing
5,598 studies on the registry are indexed under Coronary Artery Disease; 957 are open to participants now.
This study's enrollment of 600 is above the median of 124 across 3,436 interventional studies indexed under Coronary Artery Disease.
Browse Coronary Artery Disease studies →Hospital de Clinicas de Porto Alegre is the lead sponsor of 450 studies on the registry; 61 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Standardized compressive dressing
Device: Standardized compressive dressing
Hemostasis with TerumoBand®
Device: Hemostasis with TerumoBand®
Standardized compressive dressing
Hemostasis with TerumoBand®
Radial artery occlusion evaluated using Barbeau's test
test immediately after hemostasis compression device withdrawal
Time frame: up to 3 hours
Vascular complications
Clinical assesment
Time frame: up to 3 hours
Radial access site pain
standardized scale
Time frame: up to 3 hours
Plan to share: Undecided
No publications or documents are linked to this record.
This study is completed, as verified in Aug 2020. You cannot join it, but the record below documents what was studied.
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Hospital de Clinicas de Porto Alegre