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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03294993
Other study ID # 20170711
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date October 1, 2017
Est. completion date September 30, 2022

Study information

Verified date November 2021
Source China Medical University, China
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators designed a study to assess whether there were any blood flow indexes change before and after radial artery puncture with doppler ultrasonography


Description:

The investigators designed a study to assess whether there were any blood flow indexes change before and after radial artery puncture with doppler ultrasonography.The indexes include Arterial Diameter,Peak Systolic Velocity,End Diastolic Velocity,Resistive Index,Pulsatility Index,Systolic/End Diastolic Ratio,Time AverageMean Velocity and Blood Flow.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date September 30, 2022
Est. primary completion date September 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Patients were included in the study if they were ethnic Chinese, between 18 and 65 years old, American Society of Anesthesiologists (ASA) physical status I or II,candidates for general anesthesia undergoing thoracic surgery Exclusion Criteria: - Patients were excluded if they do not want to cooperate with the test, had a history of upper extremity arteriosclerosis obliterans or thromboangitis obliterans,had a history of radial artery puncture or coronary artery bypass grafting,had acute vessel trauma,or had been diagnosed with Raynaud' disease,had suffered from mental or neurological disorders

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Ultrasound assess
The investigators designed a study to assess whether there were any blood flow indexes change before and after radial artery puncture with doppler ultrasonography

Locations

Country Name City State
China the First Hospital of China Medical University Shenyang Liaoning

Sponsors (1)

Lead Sponsor Collaborator
China Medical University, China

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The Change of Peak Systolic Velocity The Change of Peak Systolic Velocity before and after surgery baseline and 30 minutes after surgery
Secondary the change of modified Allen test the change of modified Allen test before and after surgery baseline and 30 minutes after surgery