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Clinical Trials/NCT07269522
NCT07269522
Completed
Not Applicable

Functional Outcomes of Arthroscopic Anterior Cruciate Ligament Reconstruction by Hamstring Graft With and Without Platelet-Rich Plasma

Muhammad Aamir Latif1 site in 1 country60 target enrollmentStarted: January 15, 2022Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
Muhammad Aamir Latif
Enrollment
60
Locations
1
Primary Endpoint
Anterior Drawer's test

Overview

Brief Summary

No local data exists regarding the outcomes of anterior cruciate ligament reconstruction by hamstring graft with and without platelet-rich plasma. This study aimed to compare the functional outcomes of arthroscopic anterior cruciate ligament reconstruction by hamstring graft with and without platelet-rich plasma.

Detailed Description

In animal studies, platelet-rich plasma has shown excellent results in accelerating the healing of the anterior cruciate ligament, but studies on human have shown varying clinical outcomes when investigating platelet-rich plasma for its effects on anterior cruciate ligament reconstruction. The findings of this study could provide important insights about the possible role of platelet-rich plasma in arthroscopic anterior cruciate ligament reconstruction by hamstring graft. to enhance early graft healing and reduce early complications, though its long-term effectiveness remains inconsistent. Studies suggest PRP may improve short-to-medium term outcomes like reduced pain and enhanced knee function,

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Any gender
  • Aged 18-40 years
  • With clinically and radiologically confirmed arthroscopic evidence of ACL injury

Exclusion Criteria

  • With comprised bilateral ACL tears
  • Lack of fitness due to associated comorbidity
  • Fractures of lower limb bones and/or spine/neurovascular injuries
  • Injuries to other knee ligaments
  • Significant knee joint arthritis
  • Local skin infections

Outcomes

Primary Outcomes

Anterior Drawer's test

Time Frame: 12 weeks

Number of patients having grade-1 on the Anterior Drawer's test

Lachman's test

Time Frame: 12 weeks

Number of patients having grade-1 on the Lysholm knee score

Lysholm knee score

Time Frame: 12 weeks

A higher Lysholm knee score was labeled as effectiveness of the treatment.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Muhammad Aamir Latif
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Muhammad Aamir Latif

Research Consultant

RESnTEC, Institute of Research

Study Sites (1)

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