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Evaluation of outcomes after tibial ostotomy, Clinical trial study

Clinical outcomes after proximal tibial ostotomy (HTO) surgery: Clinical trial study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240425061571N5
Enrollment
154
Registered
2025-04-10
Start date
2025-04-21
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Knee osteoarthritis. Osteoarthritis, unspecified site

Interventions

Intervention group: Osteotomy technique A 6 to 8 cm longitudinal skin incision was made in the anteromedial and proximal tibia from the infrapatella to the distal. After dissection of the subcutaneous

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age under 60 years Age over 14 years old Definitive diagnosis of knee osteoarthritis, as diagnosed by an orthopedic physician and grade 3 and above (moderate and severe) according to the Kellgren and Lawrence osteoarthritis classification system (4) Knee pain and disability due to osteoarthritis that significantly interferes with employment or active recreation Failure to respond to non-invasive treatments such as physical therapy and medication for 3 months

Exclusion criteria

Exclusion criteria: Narrowing of the lateral compartment cartilage space Lateral tibial subluxation of more than 1 cm Loss of bone in the inner side of the tibia of more than 2 or 3 mm Flexion contracture greater than 15 degrees Knee bending less than 90 degrees More than 20 degrees of correction required Inflammatory arthritis Significant peripheral vascular disease Pregnancy Opioid addiction Diabetes

Design outcomes

Primary

MeasureTime frame
Knee Injury and Osteoarthritis Outcome Score (KOOS). Timepoint: Twice, intervention and 6 months later. Method of measurement: Knee Injury and Osteoarthritis Outcome Score (KOOS) Questionnaire.;Hip-knee-ankle (HKA) angle. Timepoint: Twice, intervention and 6 months later. Method of measurement: Using Marco Pacs software.;Time to recovery. Timepoint: Every month after the intervention. Method of measurement: When the patient is able to walk and perform daily activities independently, without the aid of a cane or walker.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactYasin Sharifzadeh

Babol University of Medical Sciences

dryasinsharifzadeh@gmail.com+98 11 3225 2071

Outcome results

None listed

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