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Clinical study of myofascial trigger point dry needling on pain relief of knee osteoarthritis

Clinical study of myofascial trigger point dry needling on pain relief of knee osteoarthritis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042134
Enrollment
Unknown
Registered
2021-01-14
Start date
2021-02-01
Completion date
Unknown
Last updated
2021-04-12

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

Conditions

knee osteoarthritis

Interventions

experimental group:Myofascial trigger point dry needle

Sponsors

The First People's Hospital of Changde City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Aged 50-75 years, unilateral or bilateral compliance with KOA standards, unilateral or bilateral myofascial trigger points in these muscles such as quadriceps, adductors, hamstring muscle, popliteus, tibialis anterior muscles, no history of other treatment (drugs, joint injections, acupuncture, etc.) within 1 month, signed informed consent.

Exclusion criteria

Exclusion criteria: Coagulation dysfunction or taking antiplatelet drugs; severe joint inflammation with obvious redness, swelling, heat and terness; patients with severe cardiopulmonary disease, high blood pressure, mental illness, etc.; patients with rheumatism, gout and other knee joint pain diseases; cognitive dysfunction or inability to cooperate; peripheral or central nervous system injury.

Design outcomes

Primary

MeasureTime frame
NRS;

Secondary

MeasureTime frame
Western Ontario and McMaster University osteoarthritis index;

Countries

China

Contacts

Public ContactSun Wen-Qin

The First People's Hospital of Changde City

15873666967@163.com+86 15873666967

Outcome results

None listed

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