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Comparing pain intensity and range of motion after high tibial osteotomy

Comparing pain intensity and range of motion after using combination of NSAID and Acetaminophen with opioid analgesic protocol after high tibial osteotomy

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20231217060438N1
Enrollment
30
Registered
2024-01-06
Start date
2024-01-15
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Proximal Tibial Osteotomy. Subluxation and dislocation of knee

Interventions

Intervention 1: Intervention group 1: Patients assigned to the first group will receive NSAID analgesic protocol (ibuprofen) and acetaminophen. In this group, they will take 3 tablets of ibuprofen (60

Sponsors

Applied Research Center, Deputy Behdad Police Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Nima Taheri

Applied Research Center, Deputy Behdad Police Command

nimat92@yahoo.com+98 21 8123 5481

Outcome results

None listed

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