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Clinical Study on Laser Therapy Combined with PNF Technique for Treating Pain in Knee Osteoarthritis

Clinical Study on Laser Therapy Combined with PNF Technique for Treating Pain in Knee Osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116167
Enrollment
Unknown
Registered
2026-01-06
Start date
2026-01-06
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Knee osteoarthritis

Interventions

Combined treatment group:Laser combined with PNF treatment
PNF treatment group:PNF treatment
Laser Therapy Group:Laser Therapy

Sponsors

The First Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age: 50-75 years old, gender not limited; 2. Meet the diagnostic criteria for knee osteoarthritis or the diagnosis of chronic soft tissue injury of the knee joint; 3. Visual Analogue Scale (VAS) score >=4 points, disease duration >=3 months; 4. Sign informed consent and be able to complete the rehabilitation assessment and training plan.

Exclusion criteria

Exclusion criteria: 1. Severe osteoporosis (T value <=-3.0) or joint deformity; 2. Received intra-articular injection treatment within 3 months; 3. Combined with severe cardiovascular and cerebrovascular diseases (NYHA grade ?-?); 4. Cognitive dysfunction (MMSE score <= 24 points); 5. Contraindications for photosensitivity or exercise therapy.

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale (VAS);WOMAC Osteoarthritis Index;

Secondary

MeasureTime frame
Range of Motion Measurement;Muscle strength assessment;10-meter walk test;Two-minute walking distance test;Detection of C-reactive protein (CPR) inflammatory factors;

Countries

China

Contacts

Public ContactZhu Weikai

The First Affiliated Hospital of Dalian Medical University

zhuwk1018@126.com+86 411 8363 5963

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026