- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06975566
- Original Trial
Long-term Effects of Radial Artery Cannulation on Vessel Diameter, Blood Flow and Fine Motor Skills
September 13, 2026 updated by: AKIN BİLİR, Kartal City Hospital
This observational study examined changes in blood vessel diameter, blood flow, and fine motor performance after ultrasound-guided radial artery cannulation in adults undergoing elective cardiac surgery.
Ultrasound measurements of the radial and ulnar arteries and Purdue Pegboard tests of hand performance were obtained before cannulation and during follow-up for three months.
Measurements were compared over time within each participant and between the relevant arteries or hands.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This single-centre prospective longitudinal observational study was conducted in the Department of Cardiovascular Surgery at Pamukkale University Faculty of Medicine.
Adults aged 18-80 years with American Society of Anesthesiologists physical status I-III who required radial arterial monitoring during elective cardiac surgery were recruited consecutively from 22 July to 2 September 2016.
Baseline assessments were performed in all 103 enrolled participants.
Radial and ulnar artery internal diameter, peak systolic velocity, end-diastolic velocity, resistive index, pulsatility index, and mean volume flow were assessed before cannulation and at seven subsequent time points over three months.
Purdue Pegboard performance was assessed before cannulation, 10 days after baseline, and three months after baseline.
Comparisons were made within participants over time, between the radial and ulnar arteries of the cannulated arm, and between the cannulated left and non-cannulated right hands; bimanual performance was assessed separately.
Fifty participants completed all reported assessments and were included in the complete-case analysis.
The other 53 participants did not complete follow-up because of death (7), severe postoperative morbidity (13), incomplete follow-up attendance (22), or technical or organizational reasons (11).
Individual-level partial records for these 53 participants were unavailable for reanalysis.
The study received ethics committee approval on 19 July 2016, and written informed consent was obtained before study procedures.
The investigation originated as a medical specialty thesis completed in 2017 and was retrospectively registered in 2025.
Study Type
Observational
Enrollment (Actual)
103
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Adults aged 18-80 years with American Society of Anesthesiologists physical status I-III who were scheduled for elective cardiac surgery and required radial arterial monitoring at Pamukkale University Faculty of Medicine, Department of Cardiovascular Surgery.
Eligible patients were recruited consecutively from 22 July to 2 September 2016.
Description
Inclusion Criteria:
- Age 18-80 years.
- American Society of Anesthesiologists physical status I-III.
- Scheduled for elective cardiac surgery, including coronary artery bypass grafting, valve surgery, the Bentall procedure, or atrial septal defect repair.
- Requirement for radial arterial monitoring.
Exclusion Criteria:
- Emergency surgery.
- Haemodynamic instability.
- Planned femoral arterial cannulation.
- Body mass index >35 kg/m².
- Peripheral vascular disease.
- Infection at the puncture site.
- An abnormal pulse-oximetry-assisted modified Allen screening result.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in radial and ulnar artery diameter and Doppler parameters over three months
Time Frame: Before cannulation (T0); 1 minute after anesthesia induction (T1); 30 minutes after cannulation (T2); postoperative day 1 (T3); 3 days after cannulation (T4); 10 days (T5), 1 month (T6), and 3 months (T7) after T0.
|
Internal anteroposterior diameter (mm), peak systolic velocity (cm/s), end-diastolic velocity (cm/s), resistive index (unitless), pulsatility index (unitless), and mean volume flow (mL/min) of the radial and ulnar arteries in the cannulated arm were measured by ultrasound.
Each value was the mean of three independent acquisitions.
Each parameter was analysed separately for changes from baseline and differences between arteries.
T1 was 1 minute after anesthesia induction following cannulation; T2 was 30 minutes after cannulation; T3 was postoperative day 1; T4 was 3 days after cannulation; T5, T6 and T7 were 10 days, 1 month and 3 months after baseline, respectively.
|
Before cannulation (T0); 1 minute after anesthesia induction (T1); 30 minutes after cannulation (T2); postoperative day 1 (T3); 3 days after cannulation (T4); 10 days (T5), 1 month (T6), and 3 months (T7) after T0.
|
|
Changes in Purdue Pegboard fine motor performance over three months
Time Frame: Before cannulation (T0), 10 days after T0 (T5), and 3 months after T0 (T7).
|
Fine motor performance was assessed using the Purdue Pegboard Test (Model 32020).
The right hand, left hand, and both hands together were tested in separate 30-second subtests.
Unilateral scores counted successfully inserted pins; bimanual scores counted completed pin pairs, with one pin placed by each hand.
Each subtest was repeated three times and the mean score was analysed.
Higher scores indicate better performance.
The left hand was the cannulated hand and the right hand was the non-cannulated hand.
Unilateral performance was compared between hands and over time; bimanual performance was analysed separately over time.
The 60-second assembly subtest was not performed.
|
Before cannulation (T0), 10 days after T0 (T5), and 3 months after T0 (T7).
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Numaguchi A, Adachi YU, Aoki Y, Ishii Y, Suzuki K, Obata Y, Sato S, Nishiwaki K, Matsuda N. Radial artery cannulation decreases the distal arterial blood flow measured by power Doppler ultrasound. J Clin Monit Comput. 2015 Oct;29(5):653-7. doi: 10.1007/s10877-014-9648-5. Epub 2014 Dec 16.
- Desrosiers J, Hebert R, Bravo G, Rochette A. Age-related changes in upper extremity performance of elderly people: a longitudinal study. Exp Gerontol. 1999 Jun;34(3):393-405. doi: 10.1016/s0531-5565(99)00018-2.
- Taneja K, Jain R, Sawhney S, Rajani M. Occlusive arterial disease of the upper extremity: colour Doppler as a screening technique and for assessment of distal circulation. Australas Radiol. 1996 Aug;40(3):226-9. doi: 10.1111/j.1440-1673.1996.tb00391.x.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 22, 2016
Primary Completion (Actual)
December 2, 2016
Study Completion (Actual)
December 2, 2016
Study Registration Dates
First Submitted
May 1, 2025
First Submitted That Met QC Criteria
May 15, 2025
First Posted (Actual)
May 16, 2025
Study Record Updates
Last Update Posted (Actual)
September 16, 2026
Last Update Submitted That Met QC Criteria
September 13, 2026
Last Verified
September 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- radial artery study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.