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NOT YET RECRUITING
NCT07815743
NA

Meniscal Repair Augmented With Leukocyte-Poor Platelet-Rich Plasma: A Prospective Comparative Clinical Study

Sponsor: Universidad Autonoma de Nuevo Leon

View on ClinicalTrials.gov

Summary

This prospective, randomized, comparative clinical study will evaluate the clinical and functional outcomes of meniscal repair augmented with intraoperative intralesional leukocyte-poor platelet-rich plasma (LP-PRP) compared with conventional meniscal repair without biological augmentation. A total of 62 participants aged 18 to 40 years undergoing meniscal repair will be assigned to either the LP-PRP group or the control group. Participants will be followed for 6 months after surgery. Clinical outcomes will include knee function assessed using the International Knee Documentation Committee (IKDC) questionnaire, pain intensity assessed using the Visual Analog Scale (VAS), time to return to usual activities, and adverse events or complications. Assessments will be performed preoperatively and during postoperative follow-up at 2 weeks, 1 month, 3 months, and 6 months.

Official title: Clinical Outcomes and Postoperative Recovery Following Meniscal Repair Augmented With Intraoperative Intralesional Leukocyte-Poor Platelet-Rich Plasma: A Prospective Comparative Clinical Study

Key Details

Gender

All

Age Range

18 Years - 40 Years

Study Type

INTERVENTIONAL

Enrollment

62

Start Date

2026-09

Completion Date

2027-10

Last Updated

2026-09-11

Healthy Volunteers

No

Conditions

Interventions

BIOLOGICAL

Leukocyte-poor platelet-rich plasma

Leukocyte-poor platelet-rich plasma (LP-PRP) will be prepared from approximately 60 mL of autologous venous blood using a standardized manual double-centrifugation technique. The LP-PRP will be activated with 10% calcium chloride and applied intraoperatively and intralesionally directly to the meniscal lesion between the sutured edges during meniscal repair.

PROCEDURE

Meniscal Repair

Participants will undergo meniscal repair using the surgical technique indicated according to the characteristics and location of the meniscal lesion. The same surgical and postoperative care principles will be applied to both study arms.

Locations (1)

Hospital Universitario "Dr. José Eleuterio González"

Monterrey, Nuevo León, Mexico