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Functional and Radiologic Outcome After Posterior Medial Meniscus Root Repair : A Randomized Controlled Trial Comparing Leukocyte-Rich Platelet Rich Plasma, Bone Marrow Aspiration Concentration And Conventional Repair

Functional and Radiologic Outcome After Posterior Medial Meniscus Root Repair : A Randomized Controlled Trial Comparing Leukocyte-Rich Platelet Rich Plasma, Bone Marrow Aspiration Concentration And Conventional Repair

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260220007
Enrollment
72
Registered
2026-02-20
Start date
2026-02-25
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Patient aged 18-70 years old that get Medial meniscus root injury Posterior Medial Meniscus root repair with Biologic augmentation

Interventions

Standard treatment in posterior medial meniscus root repair and augmentation by Platelet rich plasma ,Standard treatment in posterior medial meniscus root repair and augmentation by bone marrow aspira
Platelet Rich plasma with posterior medial meniscus root repair ,Bone marrow aspirate concentrate with posterior medial meniscus root repair ,posterior medial meniscus root repair by soft suture tech

Sponsors

Faculty of Medicine Chulalongkorn University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: age 18-70 Diagnosis Isolated Posterior Medial Meniscus root injury

Exclusion criteria

Exclusion criteria: 1Body Mass Index more than 30 kg/m2 2Knee osteoarthritis severity grade 3 and4 according to the Kellgren Lawrence grading system 3Varus malalignment with an angle greater than 5 degrees measured from a long film scanogram Ligamentous knee injury requiring ligament reconstruction surgery Lateral meniscus injury History of ipsilateral knee surgery involving the same knee with medial meniscus root injury Inability to comply with scheduled follow up visits meaning the participant cannot attend the required follow up appointments at 6 week 3 months 6 months and 12 months

Design outcomes

Primary

MeasureTime frame
healing rate 1 year percent ,Osteoarthritis progression 1 year grading 1,2,3,4

Secondary

MeasureTime frame
IKDC Lysholm KOOS score 6 week , 3 month , 6 month , 1 year out of 100

Countries

Thailand

Contacts

Public ContactSIWAT WANICHWIRIYAKIT

Faculty of Chulalongkorn University

siwat.wan@gmail.com0639878555

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026