Skip to content

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

Efficacy of ultrasound guided erector spinae plane block with or without dexmedetomidine on the postoperative analgesia in patients undergoing laparoscopic cholecystectomy -A comparative study - Nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064503
Enrollment
60
Registered
2024-03-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Administration of erector spinae plane block with 19ml 0.375 percent ropivacaine plus 1ml (0.5 microgram per kg ) dexmedetomidine bilaterally: Study population group B will receive bila

Sponsors

Dr Brahmacharimayum Diparani Devi
Lead Sponsor

Eligibility

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
1.Duration of analgesia (hours) 2.Time to first rescue analgesic 3.Total dose of rescue analgesics consumed in first 24 hours 4.Pain score using Visual analogue scale (VAS) at 0,6,12, 24 hours (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

MeasureTime frame
1.Hemodynamic profile- pulse rate, systolic blood pressure (SBP), diastolic blood pressure (DBP), mean arterial pressure (MAP) 2.Complications (postoperative): a.Hypotension and Bradycardia b.Shivering c.Nausea & vomitingTimepoint: All outcomes will be continously recorded for every 0,6,12 and 24 hours

Countries

India

Contacts

Public ContactDr Brahmacharimayum Diparani Devi

Regional Institute of Medical Sciences Imphal West

drnratansingh@gmail.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026