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Verapamil vs Heparin in Transradial Procedures

Comparison of VERapamil vs. Heparin Therapy on Procedural sUccess During Transradial Coronary Procedures (VERMUT Study)

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02454491
Acronym
VERMUT
Enrollment
418
Registered
2015-05-27
Start date
2015-05-31
Completion date
2016-09-30
Last updated
2016-10-04

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

Conditions

Heart Disease, Ischemic

Keywords

percutaneous coronary interventions, radial artery access, access site complications, verapamil, heparin

Brief summary

Transradial approach (TRA) for cardiac catheterization and percutaneous coronary interventions (PCI) is increasingly being used worldwide. At the present is unknown the cocktail of agents necessary to minimize local access site complications. The investigators planned a prospective randomized clinical trial to test the superiority of verapamil vs. heparin in the reduction of access site related complications.

Detailed description

Transradial approach (TRA) for cardiac catheterization and percutaneous coronary interventions (PCI) is increasingly being used worldwide in both elective and emergency procedures because it reduces net adverse clinical events, through a reduction in major bleeding and all-cause mortality, when compared to transfemoral approach. However, radial artery occlusion (RAO) after the procedure (the incidence of which varies from 1% to 10%) remains one of the major limitations of TRA. The aim of the study is to assess the superiority of verapamil versus heparin in the access success during transradial percutaneous coronary interventions (PCI). METHODS Patients referred to the cath-lab of the Cardiovascular Institute of the University Hospital of Ferrara, Italy, for coronary angiography were randomized in 2 groups with a computer-generated random sequence. The study is double-blind. In the first group, patients received intravenous heparin (5000 UI) immediately after a 6 F sheath insertion. In the second group, patients received Verapamil (5 mg) immediately after a 6 F sheath insertion. If after the start of the procedure a radial artery spasm (RAS) occurs, the operators can choose to use bail-out a local vasodilator therapy. After sheath removal, hemostasis was obtained using a TR band (Terumo corporation, Tokyo, Japan) with a plethysmography-guided patent hemostasis technique. Radial artery patency was evaluated at 24 hours (early RAO) and 30 days after the procedure (late RAO) by ultrasound. The aim of the study is to demonstrate that verapamil administration is superior to heparin administration in the reduction of the combined endpoint (occurrence of radial artery occlusion (early RAO), access site complication, radial artery spasm (RAS) requiring local bailout use of vasodilatator) RAO will be assessed by ultrasonography by independent expert reviewer blinded to randomization The investigators defined access site complication the following items: * local haematoma superficial \<5 cm from access site; * haematoma with moderate muscle infiltration \<10 cm; * forearm haematoma and muscular infiltration below the elbow; * haematoma and muscular infiltration above the elbow; * ischemic threat (compartmental syndrome); * radial artery dissection during the procedure; The investigators defined radial artery spasm any spasm occurring during the procedure requiring the administration of local vasodilatators to allow the procedure

Interventions

DRUGHeparin

intraradial administration of heparin 5000 ui

DRUGVerapamil

intraradial administration of verapamil 5 mg

Sponsors

University Hospital of Ferrara
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

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

Inclusion criteria

Patients admitted to hospital with diagnosis of acute coronary syndrome and stable coronary artery disease according current European guidelines and with clinical indication to coronary artery angiography. * all patients receiving percutaneous coronary intervention by radial artery access as first attempt * procedures with 6F catheter

Exclusion criteria

* warfarin therapy * previous ipsilateral TRA * lack of consent * scleroderma * thrombocytopenia * or other contraindications to heparin

Design outcomes

Primary

MeasureTime frameDescription
number of participants with radial artery-related complications24 hoursoccurrence of early radial artery occlusion, access site complication, radial artery spasm (RAS) that requires the bailout use of vasodilatator

Secondary

MeasureTime frameDescription
patient's satisfaction24 hoursassessment with questionnaires of the pain and satisfaction of patients
long term patient's satisfaction30 daysassessment with questionnaires of the pain and satisfaction of patients
number of participants with each radial artery-related complication24 hoursoccurrence of each singular component of primary endpoint
late radial artery occlusion30 daysoccurrence of radial artery occlusion (late RAO)
reopening early RAO30 daysreopening of the closed radial at 24 hours.

Countries

Italy

Outcome results

None listed

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