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Effects of electrical dry needling in addition to routine physiotherapy on pain, range of motion and functional disability in patients with moderate knee osteoarthritis

Effects of electrical dry needling in addition to routine physiotherapy on pain, range of motion and functional disability in patients with moderate knee osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210321050752N5
Enrollment
92
Registered
2023-12-19
Start date
2023-01-17
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Condition 1: Pain. Condition 2: Functional disability. Pain, not elsewhere classified Limitation of activities due to disability

Interventions

Intervention 1: Intervention group: Group (B) participants will receive Electrical Dry Needling with routine physical therapy exercises. Initially Routine physical therapy exercises will be performed

Sponsors

Self Supported
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age group 30-60 years. Patients with degenerated osteoarthritis. Unilaterally, most painful knee will be treated. Moderate osteoarthritis, Grade II and III. Radiologically diagnosed knee osteoarthritis. Chronic knee pain for a duration of more than three months. Less than half hour of morning stiffness.

Exclusion criteria

Exclusion criteria: Any previous trauma, fracture, subluxation, dislocation, surgery or bony abnormalities around knee joint in the past 6 months. Cancer or Suppression of immune system. Any neurological deficits in lower extremity. Pregnancy. Any dermatological issues. Unexplained weight loss/gain. Dysfunction of bladder OR Recent infection

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Pain, range of motion and functional disability will be assess at baseline, week 4 and follow up after 2 months. Method of measurement: Numeric Pain Rating Scale (NPRS).;Functional disability. Timepoint: Pain, range of motion and functional disability will be assess at baseline, week 4 and follow up after 2 months. Method of measurement: Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC).

Countries

Pakistan

Contacts

Public ContactMuhammad Waqas

The University of Lahore

drwaqasfayyaz@gmail.com+92 323 5043603

Outcome results

None listed

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