Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ASA 1 and 2 BMI less than 30
Exclusion criteria
Exclusion criteria: Patients unwilling to enroll for the study Change in the plan of anaesthesia. Patients with a history of allergy to the drugs used in the study Patients with infection at the site of injection. Duration of surgeries extending beyond 3hrs. Neuropathy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the analgesic efficacy in terms of onset of sensory blockade of ultrasound guided Intercostobrachial Nerve Block by three different approaches - distal approach versus proximal approach versus supra-axillary approach for patients undergoing proximal humerus surgeries done via delto-pectoral approach.Timepoint: The Sensory block onset will be assessed every 2 minutes for 15 minutes via pinprick testing over the anteromedial and posteromedial upper arm. | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the ease of technique in terms of duration of procedureTimepoint: Duration of the procedure will be recorded combining Landmark identification time (USG localization of target area) and Block execution time (from needle insertion to withdrawal after injecting the drug).;To assess the incidence of ICBN block failures.Timepoint: No sensory loss after 15 min after giving block will be noted;To assess analgesic efficacy post operatively using Visual analogue scale score.Timepoint: post operatively at at 0,2,4,6,12, and 24 hours;To assess incidence of complications like hematoma, nerve injury and pneumothorax.Timepoint: while administering the nerve block | — |
Countries
India
Contacts
Aarupadaiveedu Medical college and research institute