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Clinical Trials in Egypt / NCT07787195
Starting soon Not applicable

Low-Level Laser Therapy Versus Isometric Handgrip Exercise On Arteriovenous Fistula Maturation in Hemodialysis Patients

NCT07787195 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-09
Last updated
2026-08-26

Condition(s) studied

Hemodialysis

Investigational drug(s) / intervention(s)

Low-level laser therapyIsometric handgrip exercisesStandard postoperative care

Low-level laser therapy: Patients in this group will receive low-level laser therapy using the BS-W11 semiconductor low-level laser device, which emitted a red laser at 650 nm with a power output of 5 mW per diode. The laser will be applied over the arteriovenous fistula site. Each session lasts 30 minutes and is administered three times a week for a total period of eight consecutive weeks. A trained therapist will perform all procedures, and patients were monitored for any potential adverse reactions during and after each session.

Isometric handgrip exercises: Patients will be instructed to perform daily isometric handgrip exercises using a standard squeeze ball. Patients will be positioned seated comfortably, with the forearm of the exercising limb resting on the ipsilateral thigh and the elbow maintained in slight flexion throughout the exercise, in order to minimize compensatory shoulder and elbow movement and ensure that the contraction remained isolated to the forearm muscles. The exercise protocol involves squeezing at a rate of approximately 20 squeezes per minute for a total of 30 minutes per day, at 30-40% of maximum voluntary contraction (MVC). To improve compliance, participants will be allowed to divide the daily session into two 15-minute intervals if required. The exercise program continued for 8 consecutive weeks, and patients will be instructed to maintain adherence by recording their daily sessions in a logbook

Standard postoperative care: It includes wound and dressing management (keeping the dressing dry for the initial 48-72 hours, followed by regular dressing changes and site hygiene), activity restriction (avoiding heavy lifting or direct pressure over the access site during the early postoperative period), patient education on self-palpation of the access thrill, and routine follow-up visits at approximately 1 week and 6 weeks postoperatively to assess wound healing and access patency.

Study summary

The purpose of this study is to evaluate the effectiveness of low-level laser therapy (LLLT) compared with isometric handgrip exercise and standard care in promoting vascular remodeling of arteriovenous fistulas (AVFs) among hemodialysis patients.

Eligibility

Sex
ALL
Min age
35 Years
Max age
50 Years
Healthy volunteers
No
Inclusion Criteria: * Patients of both genders. * Patient age between 35 and 50 years. * Diagnosed with chronic kidney disease (CKD) Stage 4 or 5 with a newly created radiocephalic arteriovenous fistula (RC-AVF), including both pre-dialysis patients and those temporarily receiving hemodialysis via central venous catheter pending fistula maturation. * Distal forearm cephalic vein diameter ≥ 2.5 mm in the non-dominant hand Exclusion Criteria: * History of prior vascular access surgery on the same limb. * Physical or mental disability limiting the ability to perform exercises. * Positive Allen's test. * Absent or thrombosed distal forearm cephalic vein. * Already undergoing regular exercise (including manual workers). * History of hemophilia or known coagulation disorder. * Personal or family history of cancer. * Severe cardiac disease (congestive heart failure with ejection fraction ≤ 20%). * Known central venous stenosis \> 50% on the side of planned arteriovenous fistula creation.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Cairo university Cairo Egypt

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07787195 on ClinicalTrials.gov ↗ ← All trials in Egypt