Comparative Study Between Autologous Adipose Tissue Graft Versus Microfracture for Treatment of Articular Cartilage Defects

Assiut University

Status: Not yet enrolling

Conditions: Knee Osteoarthritis

Treatments: Procedure: cartilage regeneration technique

Study type: Interventional

Funder types: Other

Identifiers

NCT05912998

MGMM

Details and patient eligibility

About

Knee arthroscopy using standard portals will be performed in three groups. Complete evaluation of all intra -articular structures will be performed followed by accurate localization of the cartilage defect and measurement of its dimensions. The cartilage lesion grading according to the International Cartilage Repair Society system (ICRS). The patients assigned for the first group will have Liposuction through a minor 1 cm incision on the abdomen to obtain adequate amount of emulsified adipose tissues (50 - 60 cc). Autologous adipose tissue will be mixed with autologous hyaline cartilage obtained from non-weight bearing areas of the knee in prepared mold. The graft will be mixed with fibrin glue and left to solidify a little. After obtaining the fashioned graft from the mold it will be fixed in to the defect site by fibrin glue through mini open approach and stability of the implant fitted in the site will evaluated by gentle cycling of the joint. During the graft preparation, a high tibial osteotomy will be performed. Patients assigned for the second group will have microfracture in association with open wedge high tibial osteotomy. Patients assigned for the third group will have open wedge high tibial osteotomy. Standard titanium T locked plate will be used to fix the open wedge osteotomy in the three groups.

Enrollment: 105 estimated patients

Sex: All

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Age group 18 to 60 years old.
• Cartilage defect size range 2-5 cm2.
• Outer Bridge classification II & III.
• Single full thickness symptomatic femoral condyles ulcer.
• Varus deformity of the affected knee 50 - 100.

Exclusion criteria

• Advanced knee osteoarthritis.
• Knee range of motion less than 1000.
• Ligamentous injury of the affected knee.
• Recent intra articular injection of any type with in last 6 months.
• Fracture around the knee.
• Inflammatory joints disorders.
• Tumors.
• Immunocompromised patients.
• Body mass index < 35
• Valgus deformed knee any degree
• Sever varus deformed knee < 10 0

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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105 participants in 3 patient groups, including a placebo group

cartilage regeneration

Active Comparator group

Description:

35 patient will have knee arthroscopy and cartilage regeneration technique and high tibial osteotomy

Treatment:

Procedure: cartilage regeneration technique

microfracture

Active Comparator group

Description:

35 patient will have knee arthroscopy and microfracture with high tibial osteotomy

Treatment:

Procedure: cartilage regeneration technique

high tibial osteotomy

Placebo Comparator group

Description:

35 patient will have knee arthroscopy and high tibial osteotomy

Treatment:

Procedure: cartilage regeneration technique