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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05920538
Other study ID # 764/2565(IRB3)
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date March 13, 2023
Est. completion date January 2024

Study information

Verified date June 2023
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 190
Est. completion date January 2024
Est. primary completion date December 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Nicardipine
Subcutaneous infiltrate drug at puncture site by ultrasound-guided
Other:
Normal saline
Subcutaneous infiltrate NSS at puncture site by ultrasound-guided

Locations

Country Name City State
Thailand Anesthesiology Department Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Success rate of radial artery cannulation since first skin puncture Success rate of radial artery cannulation since first skin puncture 10 minute from puncture at skin
Secondary radial artery diameter Pre-induction radial artery diameter, post-induction radial artery diameter, radial artery diameter after subcutaneous infiltration at 0,1,2 and 3 minute Pre-induction to 3 minute after subcutaneous infiltration
Secondary Time from first skin puncture to success cannulation Time from first skin puncture to present of arterial wave form, assessed less than 10 minutes 10 minutes
See also
  Status Clinical Trial Phase
Terminated NCT02557828 - Target Sign vs Palpation for Radial Arterial Line Placement N/A
Recruiting NCT03042663 - Effect of Stellate Ganglion Block on Blood Flow in the Cannulated Radial Artery N/A
Recruiting NCT05459792 - Comparative Study Between the Effect of Ultrasound Guided Median Nerve Block , Radial Nerve Block and Local Infiltration on Feasibility of Radial Artery Cannulation N/A
Completed NCT04617106 - Radial Artery Cannulation Using Two Different Methods. N/A