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Comparison of 2 Hemostasis Techniques After Transradial Coronary

Effect of Two Compression Devices on the Occurrence of Artery Occlusion After Transradial Cardiac Catheterization: Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02873871
Enrollment
600
Registered
2016-08-22
Start date
2015-08-31
Completion date
2017-12-31
Last updated
2020-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease With Myocardial Infarction

Brief summary

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.

Detailed description

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

Interventions

DEVICEStandardized compressive dressing

Standardized compressive dressing

DEVICEHemostasis with TerumoBand®

Hemostasis with TerumoBand®

Sponsors

Hospital de Clinicas de Porto Alegre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Adult patients submitted to elective or urgent coronary catheterization who presented with a A, B or C curve on oximetry test before the procedure

Exclusion criteria

* Inability to understand the study and sign the informed consent form

Design outcomes

Primary

MeasureTime frameDescription
Radial artery occlusion evaluated using Barbeau's testup to 3 hourstest immediately after hemostasis compression device withdrawal

Secondary

MeasureTime frameDescription
Vascular complicationsup to 3 hoursClinical assesment
Radial access site painup to 3 hoursstandardized scale

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026