compare the postoperative pain intensity between pethidine and paracetamol (Aptol) recipients with tibial fractures who underwent nailing surgery. pain, pethidine, paracetamol, fractures
Conditions
Interventions
(1 mg / kg body weight) were injected half an hour before 6, 12 and 24 hours after surgery under local anesthesia.,paracetamol group (15 mg / kg body weight) were injected half an hour before 6, 12 an
Experimental Drug,Active Comparator Drug
pethidine group ,paracetamol group
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: 1. Patients with tibial fracture over 18 years of age and under 50 years of age who were candidates for tibial nail surgery. 2. Patients with tibial fracture who were classified into 42a, 42b and 42c groups according to AO classification.
Exclusion criteria
Exclusion criteria: 1. Any contraindications to paracetamol include liver disease and allergies 2. Any contraindications to the use of pethidine, including respiratory and drug-sensitive diseases. 3. If it is not possible to use the tibial nailing (such as fractures at the end and beginning of the tibia bone that cannot be nailed, or the tibial canal diameter is less than 8mm and thus, the nail cannot pass, or the tibia physe is open where nailing is forbidden). 4. Lack of consent to participate in the research project 5. Age over 50 years 6. Opium consumption 7. History of substance abuse (addicts) 8. People who received analgesics for any reason.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| postoperative pain intensity 12 and 24 hours after surgery VAS scores | — |
Secondary
| Measure | Time frame |
|---|---|
| N/A N/A N/A | — |
Countries
Iran
Contacts
Public ContactFarzaneh Fazeli
Assistant Professor Of Intensive Care, North Khorasan University of Medical Sciences,Bojnord, Iran
Outcome results
None listed