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ltrasound guided erector spinae plane block with or without dexmedetomidine on the postoperative pain in patients undergoing laparoscopic gallbladder removal

Phase 3
Conditions
Health Condition 1: O- Medical and SurgicalHealth Condition 2: O- Medical and Surgical
Registration Number
CTRI/2024/03/064503
Lead Sponsor
Dr Brahmacharimayum Diparani Devi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

a.Patients of either gender,

b. American Society of Anaesthesiologists (ASA) physical status I or II ,

c. Age 18-60 years

d. BMI (Body mass index): 18-25kg/m

Exclusion Criteria

a.Patient refusal and allergic to study drugs (local anaesthetics)

b. Bleeding disorder-platelet count

less than 50,000/microlitre, prothrombin time more than 14 sec and International normalised ratio (INR) more than 1.5

c. Local site infection and with neurological deficits of lower limb and torso

d. Cardiac, respiratory diseases, kidney disorders, pregnancy and spinal deformity

and mental/cognitive impairment

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Duration of analgesia (hours) <br/ ><br> 2.Time to first rescue analgesic <br/ ><br> 3.Total dose of rescue analgesics consumed in first 24 hours <br/ ><br> 4.Pain score using Visual analogue scale (VAS) at 0,6,12, 24 hours <br/ ><br> (postoperative)Timepoint: Outcomes will be recorded at 0,6,12, and 24 hours. Data collected will be assessed at the end of one year
Secondary Outcome Measures
NameTimeMethod
1.Hemodynamic profile- pulse rate, systolic blood pressure (SBP), diastolic <br/ ><br> blood pressure (DBP), mean arterial pressure (MAP) <br/ ><br> <br/ ><br> 2.Complications (postoperative): <br/ ><br> a.Hypotension and Bradycardia <br/ ><br> b.Shivering <br/ ><br> c.Nausea & vomitingTimepoint: All outcomes will be continously recorded for every 0,6,12 and 24 hours
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