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Thoracic epidural analgesia and ultrasound guided erector spinae plane block for pain control after Laparoscopic cholecystectomy

Comparision of thoracic epidural analgesia and ultrasound guided erector spinae plane block for post-operative pain control following laparoscopic cholecystectomy :A RANDOMIZED CLINICAL TRIAL - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/081249
Enrollment
80
Registered
2025-02-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: K802- Calculus of gallbladder without cholecystitis

Interventions

Intervention1: Administration of erector spinae plane block with 15ml 0.2 percent ropivacaine plus 0.75ml(7.5microgram) dexmedetomidine bilaterally immediately after intubation over a total period of

Sponsors

Lippi Lollen
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a. Patients of either sex b. Age group- 18 to 60 yrs. c. American society of anesthesiologists (ASA) Grade I or Grade II d. BMI: 18 to 30 kg/m2 e. Weight:40-70 kg

Exclusion criteria

Exclusion criteria: a. Patient refusal b. An allergy to local anaesthetics c. Contraindication to epidural anaesthesia (abnormal coagulation status, a local infection, preexisting neurological deficit of torso or lower limb, and spinal diseases) d. Pregnancy e. 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 24hours 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 and vomiting Timepoint: All outcomes will be continously recorded for every 0,6,12 and 24 hours.Data collected will be assessed at the end of one year

Countries

India

Contacts

Public ContactDr Laithangbam Pradipkumar Singh

Regional institute of medical sciences,Imphal West

drlaithangba@gmail.com7005238251

Outcome results

None listed

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