ClinicalTrials.Veeva

Menu

Effects of Subcutaneously Infiltrated Nicardipine on the Success Rate of Radial Artety Cannulation

M

Mahidol University

Status

Invitation-only

Conditions

Radial Artery Cannulation

Treatments

Other: Normal saline
Drug: Nicardipine

Study type

Interventional

Funder types

Other

Identifiers

NCT05920538
764/2565(IRB3)

Details and patient eligibility

About

The goal of this study is to compare the success rate of subcutaneously infiltrated nicardipine to normal saline in radial artery cannulation

Enrollment

190 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age 18-75 years
  • the patient who need to arterial line

Exclusion criteria

  • allergy to nicardipine
  • history of peripheral artery disease
  • BMI > 40 kg/m2
  • unwilling to participate or denial of informed consent

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

190 participants in 2 patient groups, including a placebo group

Nicardipine
Experimental group
Description:
Using nicardipine 0.5 mg(0.5ml) subcutaneously infiltrated by ultrasound before redial artery cannulation.
Treatment:
Drug: Nicardipine
Normal saline
Placebo Comparator group
Description:
Using normal saline 0.5ml subcutaneously infiltrated by ultrasound before redial artery cannulation
Treatment:
Other: Normal saline

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems