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Study on the therapeutic effect and kinematic characteristics of acupotomy combined with platelet-rich plasma in patients after meniscus injury

Study on the therapeutic effect and kinematic characteristics of acupotomy combined with platelet-rich plasma in patients after meniscus injury

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073365
Enrollment
Unknown
Registered
2023-07-07
Start date
2023-07-07
Completion date
Unknown
Last updated
2023-07-10

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

Conditions

Patients after meniscus arthroscopy

Interventions

group A:Acupotomy combined with PRP
group B:PRP

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged from 15 to 60 years old; 2. Meniscus injury was diagnosed, indicating arthroscopic surgery; 3. Sign subject informed consent; 4. Not included in other clinical studies.

Exclusion criteria

Exclusion criteria: 1. Patients with severe knee deformity, congenital dysplasia of meniscus, knee tumor, etc.; 2. Patients with cruciate ligament fracture, femoral condyle fracture, tibial fracture and other injuries; 3. Patients with severe osteoporosis; 4. Patients with serious life-threatening primary diseases such as cardiovascular and cerebrovascular, liver, kidney, hematopoietic system, endocrine system and mental illness; 5. Women who are breastfeeding, pregnant or planning to become pregnant, allergic or allergic to PRP; 6. Patients with rejection or adverse reactions to small needle knives; 7. Failure to provide informed consent documents or regular follow-up visits.

Design outcomes

Primary

MeasureTime frame
Lysholm score;

Secondary

MeasureTime frame
VAS score;Barthel;Clinical efficacy;

Countries

China

Contacts

Public ContactLin Zhong Hua

Fujian Provincial Hospital

doctor_lzh71@163.com+86 137 7451 1377

Outcome results

None listed

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