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Clinical evaluation of of osteochondral regeneration using silk fibroin and collagen scaffolds

Clinical evaluation of osteochondral regeneration using autologous chondrocytes seeded in bilayered

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017062434731N1
Enrollment
15
Registered
2017-07-27
Start date
2017-07-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Osteochondral defects.

Interventions

Evaluation of the safety and effectiveness of the autologous chondrocytes seeded in bilayered scaffolds based on silk fibroin and collagen in presence of growth factors in the treatment of osteochondr
Treatment - Surgery

Sponsors

Avicenna Research Institute
Lead Sponsor
scientific and technological department of presidential office
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: female or male; within the age range of 18 to 65 years; symptomatic osteochondral lesion of the medial or lateral femoral condyles with ICRS grade 3-4 lesion. Exclusion Criteria: meniscus removal with surgical treatment; knee non corrected instability; diagnosis with metastatic diseases or malignant diseases; pregnancy or breast feeding, history of neurological disease; history of endocrinological disorders such as diabetes; history of pulmonary heart diseases; infectious diseases such as hepatitis B and C, HIV and history of allergic diseases.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Radiological and Clinical Studies. Timepoint: Before intervention and 6 months and 1 year after intervention. Method of measurement: Radiographic images.;MRI studies. Timepoint: Before intervention and 6 months and 1 year after intervention. Method of measurement: MRI results.

Secondary

MeasureTime frame
Pain in the surgical area. Timepoint: after intervention. Method of measurement: Based on available evidence.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Somaieh Kazemnejadi

Avicenna Research Institute

kazemnejad_s@yahoo.com+98 21 2243 2020

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026