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Far infrared therapy on preoperative vein dilatation in arteriovenous fistula creation. A single-centre randomised controlled trial.

Far infrared therapy on preoperative vein dilatation in arteriovenous fistula creation. A single-centre randomised controlled trial.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250704001
Enrollment
44
Registered
2025-07-04
Start date
2023-01-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic kidney disease Arteriovenous fistula creation Small vein diameter Far infrared therapy Arteriovenous fistula creation Isometric handgrip exercise

Interventions

For intervention group, patients were advised on the instruction of use for the far infrared-emitting portable device. Patients underwent FIR therapy for 3 times a week, 40 minutes each session and ad
Experimental Radiation,Active Comparator Other
Far infrared therapy,Control

Sponsors

Research Ethics Committee (REC)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Cephalic vein size 1.6 to 1.9 mm with no evidence of thrombosis on duplex ultrasonography 2. Artery size of at least 2.0 mm 3. Planning for brachiocephalic fistula.

Exclusion criteria

Exclusion criteria: 1. Any complex vascular procedure such as redo procedure, brachiobasilic fistula or arteriovenous graft procedure 2. History of large vessel thrombosis 3. Known cardiovascular dysfunction (hypotension SBP less than 90 mmHg, diagnosed myocardial infarction within last 6 months, LVEF less than 35%, obstructive cardiomyopathy, severe aortic stenosis where gradient more than 40 mmHg) 4. Patient on anticoagulant.

Design outcomes

Primary

MeasureTime frame
Change in cephalic vein diameter 1 month post intervention millimetre

Secondary

MeasureTime frame
Change in brachial artery diameter 1 month post intervention millimetre,Number of patients achieving 2 millimeter cephalic vein diameter 1 month post intervention Frequency,Maturation rate 6 weeks post-BCF creation Frequency

Countries

Malaysia

Contacts

Public ContactChoon Wei Ngo

Universiti Kebangsaan Malaysia

choonwei1991@gmail.com03 9145 5555

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026