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Comparison of efficacy of local application of local anesthetic drug with additives for pain relief after laparoscopic cholecystectomy surgery.

Comparison of efficacy of intraperitoneal instillation of Ropivacaine with Dexmedetomidine vs Ropivacaine with Dexamethasone for pain relief after laparoscopic cholecystectomy; a prospective randomized, double blind study. - Intraperitoneal infiltration

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065825
Enrollment
120
Registered
2024-04-16
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Interventions

Intervention1: Ropivacaine with Dexamethasone: After the completion of surgery, 40 ml of 0.2% Ropivacaine and 1 mcg/kg Dexmedetomidine will be instilled via trocar in the gallbladder fossa. Post-insti

Sponsors

Department of Anesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 and 2 patients Age: 18 - 59 years Patients undergoing elective laparoscopic cholecystectomy surgery Patients who are able to interpret Numerical rating scale scoring

Exclusion criteria

Exclusion criteria: Presence of acute cholecystitis, and choledocholithiasis. Patients on steroids Pregnant and lactating women Patients who have undergone previous abdominal surgery. Laparoscopy getting converted to open surgeries History of allergies to medications Patient on beta blockers Duration of surgery: more than 3 hours

Design outcomes

Primary

MeasureTime frame
To access the postoperative analgesia using NRS score in patients undergoing laparoscopic cholecystectomy using intraperitoneal instillation of ropivacaine and dexmedetomidine vs ropivacaine and dexamethasoneTimepoint: Using NRS, the post-operative pain intensity will be measured for each patient at rest and during movement at 20 mins, 30mins, 1 hour, 2, 4, 6, 12, and 24 hours from the time of extubation.

Secondary

MeasureTime frame
To assess incidence of Postoperative nausea and vomiting and Sedation scoreTimepoint: Patient will be assessed at 20, 30 mins, 1,2,4,6,12,24 hours;To assess the time required for the first rescue analgesia And the total dose of rescue analgesia over 24 hours Timepoint: NRS scoring will be recorded 1,2,4,6,12,24 hours post operaatively.

Countries

India

Contacts

Public ContactDr Johnson P Abraham

St Johns medical College Hospital, Bangalore

drshilpa.josh@gmail.com9901405136

Outcome results

None listed

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