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Effects of Platelet-Rich Fibrin in Patients With Anterior Cruciate Ligament Reconstruction

H

Hacettepe University

Status and phase

Completed
Phase 4

Conditions

Effects of Platelet-Rich Fibrin on Knee Stability and Knee Function

Treatments

Other: Standard ACL reconstruction surgery
Biological: Platelet-Rich Fibrin during Standard ACL reconstruction surgery

Study type

Interventional

Funder types

Other

Identifiers

NCT05904158
E-18-2060

Details and patient eligibility

About

The study was conducted to investigate the effects of platelet-rich fibrin on knee stability, knee muscle strength and knee function in patients with ACL reconstruction. Thirty patients with ACL reconstruction were included to the study and randomly divided into two groups. Patients were assessed preoperative and at the postoperative 1-year.

Full description

The study was conducted yo investigate the effects of platelet-rich fibrin (PRF) on the knee stability and function in patients with anterior cruciate ligament (ACL) reconstruction. Thirty patients with ACL reconstruction were included to the study and randomly divided into two groups (PRF group and control group). Hamstring tendon autograft was used in all patients for the reconstruction of the teared ACL. A standardized postoperative rehabilitation program was applied to all patients. Patients' knee stability, knee muscle strength and knee function were assessed preoperatively and one-year postoperatively. Knee stability was assessed using KT-2000 Knee Arthrometer. Quadriceps femoris and hamstring muscle strength measurements were conducted with an isokinetic dynamometer at 60˚/sec and 180˚/sec angular velocities. One Leg Hop (OLH) and Y-Balance tests, and International Knee Documentation Committee (IKDC) were used to evaluate the knee function.

Enrollment

30 patients

Sex

All

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Being isolated ACL reconstruction,
  • Being between the ages of 18-45 years,
  • Performing sports recreationally or professionally

Exclusion criteria

  • Having previous knee surgery,
  • Having systematic disease,
  • Having multiple ligament injury on the knee or additional cartilage injuries

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

PRF Group
Experimental group
Description:
Patients in this group, received PRF application during the standard ACL reconstruction surgery
Treatment:
Biological: Platelet-Rich Fibrin during Standard ACL reconstruction surgery
Control Group
Active Comparator group
Description:
Patients in this group received a standard ACL reconstruction surgery without any other intervention.
Treatment:
Other: Standard ACL reconstruction surgery

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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