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Comparing the effectiveness of dry needling and ischemic pressure on trigger points in knee osteoarthritis patients

Comparing the effectiveness of dry needling and ischemic compression on the trigger points of the lower half muscles behind the knee on pain and disability and muscle and joint stiffness in knee osteoarthritis patients: randomized clinical trial single-blind

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170715035097N2
Enrollment
60
Registered
2023-04-13
Start date
2023-05-01
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Knee osteoarthritis. Bilateral primary osteoarthritis of knee

Interventions

Intervention 1: First intervention group: 3 sessions of dry needling twice a week on trigger points plus10 daily routine physiotherapy sessions (Includes 20 minutes of conventional TENS with a frequen

Sponsors

University of social welfare and rehabilitation sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 70 Years

Inclusion criteria

Inclusion criteria: Mild to moderate severity of osteoarthritis (grade I-III in the Kellgren-Lawrence scale) The presence of at least one trigger point (latent or active) in the gastrocnemius and popliteus muscles based on the criteria of Travell and Simons, which can be detected by touch. Age between 50-70 years The pain level of knee osteoarthritis patients should be higher than 30 mm and less than 80 mm on the VAS scale and at least 3 months have passed since its onset. Morning joint stiffness less than 30 minutes

Exclusion criteria

Exclusion criteria: Severe inflammation/swelling of the knee Any previous fracture or surgery of the lower limb Systemic disease (such as rheumatoid arthritis or diabetes) Contraindications to using dry needling, including pregnancy, malignancy, fear of needles, bleeding disorders (such as hemophilia or thalassemia), taking antiplatelet and anticoagulant drugs Complete replacement of the knee joint on the affected side Injection of opioid analgesics or corticosteroids in the last 30 days Fibromyalgia syndrome Physical therapy or dry needling in the last 3 months Radiculopathy/myopathy

Design outcomes

Primary

MeasureTime frame
Pain Intensity. Timepoint: Before the intervention - immediately after the end of the intervention. Method of measurement: Visual Analog Scale.

Secondary

MeasureTime frame
Disability. Timepoint: Before the intervention - immediately after the end of the intervention. Method of measurement: Knee injury and Osteoartritis Outcome Score questionnaire.;Muscle stiffness. Timepoint: Before the intervention - immediately after the end of the intervention. Method of measurement: Shear wave elastosonography.;Joint stiffness. Timepoint: Before the intervention - immediately after the end of the intervention. Method of measurement: Electrogoniometer and pendulum test.;Pressure pain threshold. Timepoint: Before the intervention - immediately after the end of the intervention. Method of measurement: Algometer.;Rang Of Motion. Timepoint: Before the intervention - immediately after the end of the intervention. Method of measurement: Standard goniometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohsen Shams

University of social welfare and rehabilitation sciences

mohsenshams48@yahoo.com+98 21 7736 4525

Outcome results

None listed

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