Prospective randomized controlled trial of PRP for postoperative pain after anterior cruciate ligament fracture reconstruction

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300067737

Enrollment

Unknown

Registered

2023-01-19

Start date

2023-01-20

Completion date

Unknown

Last updated

2023-05-15

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

Conditions

Pain after anterior cruciate ligament reconstruction.

Interventions

Study group:Rehabilitation, PRP intraarticular injection

Control group:Rehabilitation

Eligibility

Sex/Gender

All

Age

18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Patients with symptomatic and MRI findings that met diagnostic criteria for ACL rupture; 2. Aged 18-50 years, male or female; 3. Informed consent for the study; 4. Knee arthroscopy during hospitalization.

Exclusion criteria

Exclusion criteria: 1. Women in pregnancy or lactation; 2. Severe fractures or stiffness of joints elsewhere; 3. Patients undergoing secondary surgery.

Design outcomes

Primary

Measure	Time frame
visual analogue scale;The Lysholm score;International Knee Documentation Committee (IKDC) score;MR;	—

Secondary

Measure	Time frame
C-reactive protein;Erythrocyte sedimentation rate;	—

Countries

China

Contacts

Public ContactMinghua Zhang

Longyan First Affiliated Hospital of Fujian Medical University

zmh86109@126.com+86 15280811355

Outcome results

None listed

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