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