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The effect of dry needling on pain and disability in total knee arthroplasty patients.

The effect of dry needling on pain and disability in total knee arthroplasty patients with active trigger points in knee muscles: a clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180716040489N1
Enrollment
25
Registered
2019-01-15
Start date
2018-08-04
Completion date
Unknown
Last updated
2019-01-29

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

Conditions

Total knee arthroplasty.

Interventions

Intervention group: Active trigger points were explored in Muscles surrounding the knee. Patients with active trigger points who fullfilled inclusion/exclusion criteria underwent one dry needling sess

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to 80 Years

Inclusion criteria

Inclusion criteria: Having total knee athroplasty Having Active Trigger Point in Knee Muscles such as Quadriceps , Hamstring,Gastrosoleus Having visual analogue scale (VAS) > 40 Age between 55 to 80 years old Having knee full extension The ability to read and write

Exclusion criteria

Exclusion criteria: Having radicular pain or neuropathy Having fibromyalgia, hypothyroedism, meralgia parethesia Having systemic disease or myopathy or malignancy Fear of needling Taking anticoagulants Taking NSAIDs Total hip arthroplasty in the same side Painful total knee arthroplasty in opposite side less than 6 month ago

Design outcomes

Primary

MeasureTime frame
Pain score. Timepoint: one week and one month after treatment. Method of measurement: pain is investigated by Visual Analoge Scale .;Function score by Knee injury and Osteoarthritis Outcome Score(KOOS). Timepoint: one week and one month after treatment. Method of measurement: .FUNCTION IS Investigated by Knee injury and Osteoarthritis Outcome Score(KOOS).

Secondary

MeasureTime frame
Knee diability. Timepoint: Before the intervention, one week and one month after treatment. Method of measurement: Knee injury and Osteoarthritis Outcome Score.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Bagher Mashaheri Fard

Esfahan University of Medical Sciences

momashaheri@rehab.mui.ac.ir+98 31 3228 9115

Outcome results

None listed

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