Comparing pain intensity and range of motion after high tibial osteotomy

Phase 2

Recruiting

• Conditions: Proximal Tibial Osteotomy.; Subluxation and dislocation of knee; S83.1

• Registration Number: IRCT20231217060438N1
• Lead Sponsor: Applied Research Center, Deputy Behdad Police Command

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 January 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Patients undergoing proximal tibial osteotomy
Physically active people
Age range of 20 to 50 years

Exclusion Criteria

having pain and range of motion outside the study limit before the operation
Drug addiction
Having a history of drug sensitivity to ibuprofen, acetaminophen, and oxycodone
Patients with BMI higher than 40
Patients with a history of taking corticosteroid drugs
Patients with a history of osteoporosis
A patient who gets an infection after surgery
A patient who is hospitalized again within three months
A patient who receives a pain pump after surgery
Sedentary people (less than 2 hours of physical activity per day) or with high activity such as runners (more than 10 hours of physical activity per day)
Having a disorder in the knee ligaments
Having severe DJD

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Intensity of pain. Timepoint: 1, 2, 7, 30, 90 days after surgery. Method of measurement: Visual Analogue Scale (VAS).;Range of motion. Timepoint: 1? 2? 7? 30? 90 days after surgery. Method of measurement: Orthopedic gonia.