Health Condition 1: S622- Fracture of first metacarpal bone Health Condition 2: S622- Fracture of first metacarpal bone Health Condition 3: S424- Fracture of lower end of humerus Health Condition 4: S525- Fracture of lower end of radius Health Condition 5: S526- Fracture of lower end of ulna Health Condition 6: S620- Fracture of navicular [scaphoid] bone of wrist Health Condition 7: S621- Fracture of other and unspecifiedcarpal bone(s) Health Condition 8: S626- Fracture of other and unspecifiedf
Conditions
Interventions
Intervention1: Opioid Free Analgesia: opioid free analgesics
1)Diclofenac sodium oral- 50mg per dose twice daily i/v- 75mg per dose twice daily
( max dose of 150mg per day)
Sponsors
Katikareddy Sai Abhiram Reddy
Eligibility
Inclusion criteria
Inclusion criteria: 1. Age above 18 years. 2. Scheduled for unilateral upper limb bony orthopedic surgery. 3. Provision of informed consent to participate in the study.
Exclusion criteria
Exclusion criteria: 1.Patients undergoing revision surgery. 2.Patients requiring bone grafting from site other than operative limb 3.Patients with open fractures. 4.Polytrauma patients.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.To assess the difference in pain level using NPRS at 6 hours,12 hours, 24hours after upper limb bony orthopedic surgery in patients receiving opioid based versus opioid free analgesia.Timepoint: 6hours, 12 hours,24 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To assess the patient satisfaction with post operative pain control at 2 weeks using numeric rating scale 2. To assess the incidence of various adverse drug reactions of analgesics Timepoint: 2 weeks | — |
Countries
India
Contacts
Public ContactDrJohn A Santoshi
All india institute of medical sciences,Bhopal
Outcome results
None listed