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Clinical Trials/NCT07584603
NCT07584603Not yet recruitingNot Applicable

The Role of High-intensity Laser Therapy on Femoral Cartilage Thickness in Patients With Knee Osteoarthritis

University of Lahore1 site in 1 country58 target enrollmentStarted: July 1, 2026Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
58
Locations
1

Study Overview

Brief Summary

This clinical trial will evaluate the effects of High-Intensity Laser Therapy (HILT) on femoral cartilage thickness and other clinical outcomes in people with knee osteoarthritis. Participants aged 40 to 60 years with grade II or III knee osteoarthritis will be randomly assigned to receive either HILT plus conventional physiotherapy or conventional physiotherapy alone. Both groups will receive 12 treatment sessions on alternate days for 4 weeks. The study will assess changes in cartilage thickness using ultrasound, as well as improvements in pain, knee movement, muscle strength, and daily function. Findings from this research may help improve physiotherapy treatment strategies for patients with knee osteoarthritis.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Masking Description

This is a single-blind study. The outcome assessor will be blinded to group allocation, while the participants and treating physiotherapist will be aware of the intervention assigned

Eligibility Criteria

Ages
40 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Male and female participants aged 40-60 years.
  • Diagnosed with knee osteoarthritis (Kellgren-Lawrence grade II or III).
  • Knee pain for at least 3 months.
  • Visual Analogue Scale (VAS) score ≥
  • Willing to provide written informed consent and comply with treatment and follow-up schedule.

Exclusion Criteria

  • History of knee surgery or traumatic knee injury.
  • Inflammatory arthritis (e.g., gout, psoriatic arthritis).
  • History of cancer or psychiatric illness.
  • Cognitive disorders (e.g., Parkinson's disease, Alzheimer's disease).
  • Severe comorbidities limiting exercise (e.g., severe COPD, heart failure, cerebrovascular event).
  • Hip or ankle joint disability.
  • Intra-articular knee injection within the past 3 months.

Investigators

Sponsor
University of Lahore
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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