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The Effect of Postoperative injection of platelet-rich plasma on knee edema and adhesion, and graft revascularization

The Effect of Postoperative injection of platelet-rich plasma on knee edema and adhesion, and graft revascularization

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040262
Enrollment
Unknown
Registered
2020-11-26
Start date
2020-12-01
Completion date
Unknown
Last updated
2022-03-07

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

Conditions

Knee anterior cruciate ligament injury

Interventions

PRP group:PRP injection 4w, 8w & 12w after surgery
Control group:No postoperative PRP injection

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Patients with ACL injury confirmed by imaging and knee arthroscopy who are scheduled to undergo ACLR; 2. Aged 16-45 years old, femoral and tibial epiphyses are closed; 3. The range of motion of the knee joint is basically restored before the operation (reach nearly full extension and bent over 120 degree); 4. Volunteer to participate in the research and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Multiple ligament injuries caused by severe trauma (combined with posterior cruciate ligament injury, posterolateral structural injury, medial patellofemoral ligament injury, and medial collateral ligament injury of degree II or higher); 2. Bilateral ACL injury or contralateral knee dysfunction; 3. Combined with tibial plateau fracture, severe cartilage damage, meniscus repair, and osteoarthritis; 4. Past surgery history of the knee joint (ipsilateral and contralateral); 5. Combined with other system diseases, such as malignant tumors, blood system, rheumatism and endocrine and metabolic diseases; 6. History of infectious diseases transmitted through blood, such as HIV, HBV, HCV, syphilis infection, etc.; 7. Children under 16 years old, pregnant and lactating women; 8. History of drug and alcohol abuse, cognitive dysfunction and history of mental illness; 9. Other situations that cannot cooperate with postoperative medication and rehabilitation and completion of follow-up.

Design outcomes

Primary

MeasureTime frame
KOOS4 (symptoms, pain, sports and recreation, quality of life);

Secondary

MeasureTime frame
GROC (-7~+7);KOOS (5 subscales);Knee ROM;Knee circumference;MRI indicators (i.e. SNQ);P4 (VAS at 4 timepoints);PROs (Tegner, Lysholm, IKDC scores);Objective tests (ADT, Lachman, PST, KT-1000);

Countries

China

Contacts

Public ContactZhao Jinzhong

Shanghai Sixth People's Hospital

jzzhao@sjtu.edu.cn+86 18930177160

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026