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se of Ultrasound to give pain relief will be tested in patients who are morbidly obese and are undergoing surgery

Not Applicable
Conditions
Health Condition 1: null- Morbidly Obese patients undergoing Bariatric Surgery
Registration Number
CTRI/2011/12/002267
Lead Sponsor
Max Super Speciality Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
100
Inclusion Criteria

BMI > 35 Kg/m2

Either Gender

Posted for Laparoscopic bariatric surgery

Under general anaesthesia

Exclusion Criteria

1.Any relevant drug allergy

2.Seizure disorder

3.Antidepressants

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Requirement of Tramazac hydrochloride in first 24 hours after surgeryTimepoint: Requirement of Tramazac hydrochloride in first 24 hours after surgery
Secondary Outcome Measures
NameTimeMethod
: VAS score, RASS ((Richmond Agitation - Sedation Scale; table 1), time to ambulate, adverse eventsTimepoint: First 24 hours from end of surgery
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