ew block technique for brachial block for upper limb surgery
Phase 1
- Conditions
- Health Condition 1: null- Inclusion criteria:Patients between 18 to 60 years ASA grades Iâ??III patientsExclusion criteria: Patient refusalKnown peripheral neuropathyHepatic or renal insufficiencyCoagulopathy
- Registration Number
- CTRI/2017/08/009483
- Lead Sponsor
- Department of AnaesthesiaESI Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients between 18 to 60 years of age
Patients belonging to ASA grades Iâ??III will be included.
Exclusion Criteria
Patient refusal
Known peripheral neuropathy
Known allergy to amide local anesthetic drugs.
Hepatic or renal insufficiency
Coagulopathy
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method : Duration of sensory block.Timepoint: Pinprick anesthesia to a 23-gauge needle will be assessed by an anesthetist for 30 minutes post drug injection . It will be done every 5 min for the first 30 minutes following injection of the drug,then half hourly till recovery of block
- Secondary Outcome Measures
Name Time Method 1.Block onset time <br/ ><br>2.Onset of sensory block <br/ ><br>3.Onset of motor block <br/ ><br>4.Block efficacy will be graded as : <br/ ><br>Gr 1 successful <br/ ><br>Gr 2 partially successful <br/ ><br>Gr 3 unsuccessful <br/ ><br> <br/ ><br>5.Block performance time 6.duration of motor block of all and of individual nerves <br/ ><br>7.duration of sensory block of individual nerves <br/ ><br>8.time to first request for postop analgesia <br/ ><br>9.Post block complication <br/ ><br>Timepoint: Pinprick anesthesia to a 23-gauge needle will be assessed by an anesthetist for 30 minutes post drug injection . It will be done every 5 min for the first 30 minutes following injection of the drug,then half hourly till recovery of block