Status
Conditions
Treatments
About
This clinical study aims to explore whether a non-invasive treatment known as Low-Level Laser Therapy (LLLT) can help people with a partial tear of the anterior cruciate ligament (ACL) in their knee. The ACL is one of the major ligaments that helps stabilize the knee joint. When partially torn, it can cause knee pain, weakness, and trouble walking or doing daily activities.
Traditional physiotherapy is often used to treat ACL injuries without surgery. In this study, researchers are testing whether adding LLLT to standard physiotherapy improves outcomes more than physiotherapy alone. LLLT, also called photobiomodulation, is a painless treatment that uses low-energy laser light to reduce swelling and promote tissue healing.
The study includes 72 patients, aged 20 to 40, who have been diagnosed with a partial ACL tear. All participants will receive standard physiotherapy exercises and shortwave diathermy (a type of deep heat therapy). Half of the participants will also receive LLLT, while the other half will not.
The main goals are to see if LLLT can:
Reduce knee pain
Improve knee strength
Help patients perform daily activities more easily
Each participant will be monitored over 6 weeks, with assessments at the beginning, the 3rd week, and the 6th week. Pain levels, muscle strength, and ability to perform daily activities will be measured using standard tools.
Full description
Background & Rationale:
Partial ACL tears are a common orthopedic injury that can cause pain, instability, reduced strength, and functional disability. These injuries are frequently seen in young adults who engage in sports involving pivoting and sudden direction changes. While complete ACL tears often require surgical intervention, partial tears are typically managed conservatively through physiotherapy and other non-surgical interventions.
Low-Level Laser Therapy (LLLT), also known as photobiomodulation, has emerged as a promising treatment to enhance tissue repair, reduce inflammation, and relieve pain. It works by applying low-energy laser light to injured tissue, which stimulates cellular processes and promotes healing. Despite positive results in treating other musculoskeletal conditions, evidence specifically addressing the efficacy of LLLT for partial ACL tears remains limited.
Study Design and Methodology:
This single-blinded, randomized controlled trial includes 72 participants with MRI-confirmed partial ACL tears. Participants are between 20 and 40 years of age, and both genders are included. After screening and consent, eligible participants are randomly assigned to two groups (n=36 each):
Group A (Intervention group): Receives Low-Level Laser Therapy (LLLT) + Standard Physiotherapy + Shortwave Diathermy
Group B (Control group): Receives only Standard Physiotherapy + Shortwave Diathermy
LLLT Parameters:
Wavelength: 830 nm
Power Output: 150 mW
Power Density: 5 W/cm²
Frequency: 2-3 sessions/week for 6 weeks
Probe contact time: 3-4 minutes per site (multiple areas around knee joint)
Standard Therapy (both groups):
Exercises: Heel slides, partial knee bends, quad sets, step-ups
Frequency: 2 sets of 10 reps, rest interval 3-5 seconds
Shortwave Diathermy: 2-3 sessions, 20-30 minutes, 27.12 MHz
Outcome Measures:
Assessments will be done at baseline, 3rd week, and 6th week using the following tools:
Pain: McGill Pain Questionnaire
Strength: Handheld dynamometer for quadriceps/hamstrings
Functional Disability: KOOS (Knee injury and Osteoarthritis Outcome Score)
Blinding & Randomization:
Participants are randomized using computer software
The study is single-blinded; assessors will not know the group assignments
Ethical Considerations:
Approved by the University of Lahore Ethical Committee
Informed written consent obtained
Confidentiality, voluntary participation, and withdrawal rights ensured
Expected Impact:
This study will provide evidence on the clinical value of LLLT as an adjunct to standard rehabilitation for patients with partial ACL tears. It has the potential to guide best practices in conservative management and offer an effective, non-invasive option for improving patient outcomes without surgery.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
72 participants in 2 patient groups
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal