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Calcium Channel Blocker
Verapamil Dilution for Peripheral Vasospasm
Phase < 1
Recruiting
Led By Khalil Ibrahim, MD
Research Sponsored by University of Illinois at Chicago
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up approximately 30 minutes
Awards & highlights
Study Summary
This trial will compare the efficacy and safety of IA Verapamil diluted with normal saline to undiluted IA Nicardipine during a common heart procedure. Patients will be randomly assigned to one of two groups.
Eligible Conditions
- Burning Pain
- Peripheral Vasospasm
- Pain
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ approximately 30 minutes
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~approximately 30 minutes
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Pain After Intra-arterial Calcium Channel Blocker Administration
Pain Prior to Intra-arterial Calcium Channel Blocker Administration
Radial Artery Spasm
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: VerapamilActive Control1 Intervention
Intra-arterial Verapamil 5 mg (2mL) diluted with 8 mL of normal saline
Group II: NicardipinePlacebo Group1 Intervention
Intra-arterial Nicardipine 400 mcg undiluted (8mL)
Find a Location
Who is running the clinical trial?
University of Illinois at ChicagoLead Sponsor
614 Previous Clinical Trials
1,562,251 Total Patients Enrolled
Khalil Ibrahim, MDPrincipal InvestigatorUniversity of Illinois at Chicago
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You recently had a procedure called cardiac catheterization.
Research Study Groups:
This trial has the following groups:- Group 1: Verapamil
- Group 2: Nicardipine
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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