Health Condition 1: S529- Unspecified fracture of forearm Health Condition 2: S529- Unspecified fracture of forearm Health Condition 3: S529- Unspecified fracture of forearm Health Condition 4: O- Medical and Surgical
Conditions
Interventions
Intervention1: Group N patients will receive 25 ml of 0.5% bupivacaine with 100 µg.kg-1 of nalbuphine made as 1ml, making a total volume of 26ml.: Under strict aseptic precautions with the guidance
Sponsors
Sree Balaji Medical College and Hospital Chennai
Eligibility
Inclusion criteria
Inclusion criteria: Body weight : 50 -70 kg.
Exclusion criteria
Exclusion criteria: Patients not willing to participate. ASA 3 patients Patients with local anaesthetic allergy Patients with active infection at injection site. Patients with pre existing neurological deficit.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the efficacy in terms of duration of sensory block,onset of motor and sensory blocks.Timepoint: 1. The onset of sensory block will be assessed from the cessation of drug administration to Grade 2 level blockade. 2. The onset of motor block will be assessed from the cessation of drug administration from the cessation of drug administration to Grade 3 level blockade 3. The duration of sensory block shall be taken from the time of onset of sensory block until the pain reported first. 4. Patient’s numerical pain score will be recorded every 4 hours until upto 24 hours. | — |
Secondary
| Measure | Time frame |
|---|---|
| To record the time of first rescue analgesia and adverse adverse effects if any.Timepoint: Postoperatively,pain will be assessed every 4 hours upto 24 hours by Numerical Pain intensity scale(0 to 10). | — |
Countries
India
Contacts
Public ContactDr M Sathyasuba
Sree Balaji medical college and hospital
Outcome results
None listed