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Effect of Yuanli acupuncture combined with Hegu acupuncture on patellofemoral pain syndrome: a randomized controlled trial.

Effect of Yuanli acupuncture combined with Hegu acupuncture on patellofemoral pain syndrome: a randomized controlled trial.

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052648
Enrollment
Unknown
Registered
2021-11-03
Start date
2021-12-01
Completion date
Unknown
Last updated
2022-08-08

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

Conditions

Patellofemoral pain syndrome

Interventions

control group:Regular family training
Experimental group:Round needle and valley thorn

Sponsors

Zhejiang Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. In activities such as sitting for a long time, squatting up, going up and down stairs, jumping, running, kneeling, etc., there are at least two activities that cause pain around the knee when the patient is finished; 2. Pain at the patella; 3. Pain when walking down a 25 cm step or squatting with both legs; 4. Symptoms persist for more than 1 month; 5. Visual analogue scale (VAS) >= 3 points; 6. No obvious trauma history, involuntary attack; 7. Aged < 40 years, with unilateral disease, in order to reduce the possibility of knee osteoarthritis; 8. All patients signed the informed consent form, and this study was carried out after being approved by the hospital ethics committee.

Exclusion criteria

Exclusion criteria: 1. Those who have a history of knee trauma, fracture, ligament reconstruction and other knee surgery in the past; 2. Severe deformity of the lower extremity, combined with other organ diseases and cannot tolerate the test; 3. Combined with severe lumbar disc herniation affecting walkers; 4. Those who fail to receive acupuncture and moxibustion continuously, such as fainting acupuncture and pregnant women; 5. Patients with other diseases that may affect the experimental evaluation (rheumatoid arthritis, gout, tumor and abnormal bone metabolism, etc.).

Design outcomes

Primary

MeasureTime frame
Electromyography;

Secondary

MeasureTime frame
visual analogue scale;Lysholm knee function score ;Response evaluation;

Countries

China

Contacts

Public ContactTan Tongcai

Zhejiang Provincial People's Hospital

29ttc@sina.com+86 13588067448

Outcome results

None listed

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