Comparison of the analgesic effect of oxycodone, diclofenac, gabapenti

Phase 2

• Conditions: Tibial fracture.; Fracture of shaft of tibia; S82.2

• Registration Number: IRCT20230716058804N1
• Lead Sponsor: Directorate of Health, Rescue and Treatment of Police Headquarter of Islamic Republic of Iran

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 August 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 111

Inclusion Criteria

Candidate for tibial bone fracture repair surgery
Age: 17-65 years old
Both genders

Exclusion Criteria

The presence of coagulation disorders
Liver, kidney and heart disease
History of taking opioid drugs in the last 48 hours
Addiction to drugs and alcohol
Presence of sensitivity to the study drugs
Presence of plasma creatinine>1.5 mg/dl
Having a platelet count of less than 150,000
Having a family history of thromboembolism
The presence of severe hemodynamic instability
Reluctance to participate in the study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative pain. Timepoint: During the recovery time, 2, 4, 6, 12 and 24 hours after the operation. Method of measurement: Visual analog scale.;The amount of sedation. Timepoint: During the recovery time, 2, 4, 6, 12 and 24 hours after the operation. Method of measurement: Ramsay scale.