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feasibility of ultrasound guided superficial cervical plexus block for managing shoulder pain during laprascopic surgery under spinal anaesthesia

Phase 2
Completed
Conditions
Health Condition 1: null- Shoulder pain in Gynaecological Laprascopic surgeries under spinal anaesthesia
Registration Number
CTRI/2018/02/011666
Lead Sponsor
Anaesthesia Department
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

1. ASA physical status I and II

2. Gynaecological Laparascopic surgeries under 2hours

Exclusion Criteria

1. Contraindication for spinal anaesthesia

2. Infection in the skin of the neck

3. Height less than 145cms

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
intra operative opiod requirementTimepoint: 2 hours
Secondary Outcome Measures
NameTimeMethod
Conversion to GA <br/ ><br>Timepoint: 2 hours;Diaphragmatic function Assessment by Lloydâ??s methodTimepoint: 30 minutes;Patient satisfaction <br/ ><br>Timepoint: 3 hours
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