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Effects of 9 Points Electrical Dry Needling in Knee Osteoarthritis

This trial has no sites in United States.

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Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 40 and 60 years old?

Source: NCT07403448, who can take part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

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Trial details

Who runs it
Riphah International University
Trial code
NCT07403448
Record updated
11 February 2026
Original description
The study will be conducted to compare effects of 9 points electrical dry needling along with standard physical therapy and standard physical therapy alone in knee osteoarthritis patients.Read full original descriptionShow less

Effects of 9 Points Electrical Dry Needling on Pain, Range of Motion, Function and Quality of Life in Patients With Knee Osteoarthritis

The study will be conducted to compare effects of 9 points electrical dry needling along with standard physical therapy and standard physical therapy alone in knee osteoarthritis patients.

Inclusion: participants age group from 40-60 years; Both male and female genders; Knee osteoarthritis (OA) confirmed by radiographic evidence (Kellgren- Lawrence grade 3); Numerical Pain Rating Scale (NPRS) ≥ 4/10; Able to stand and bear weight on affected knee; WOMAC score > 25 moderate level of difficulty performing ADL; Participant with restricted range of motion; Pain while walking and ascending stairs; Patients volunteered to participate in the study and signed informed consent.

Exclusion: Recent knee surgery or injection (<6 months); Patient with needle phobia and with history of abnormal reaction to needles; Diagnosed psychological disorders; Mild to severe knee osteoarthritis (Kellgren-Lawrence grade 2 or 4); Knee instability and ligamentous injury; Pregnancy and breastfeeding; Anticoagulant patient, tumors and hematomas; All acute emergencies and acute systematic fevers; Pacemakers and implantable cardioverter defibrillators.

ClinicalTrials.gov NCT07403448