Skip to content

Comparison of Intraperitoneal Bupivacaine Alone or With Dexmedetomidine

Comparison Between Mean Duration of Post-operative Analgesia of Intraperitoneal Bupivacaine Alone or With Dexmedetomidine Following Laparoscopic Cholecystectomy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06560892
Enrollment
68
Registered
2024-08-19
Start date
2024-01-01
Completion date
2024-06-30
Last updated
2024-08-21

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

Conditions

LAPAROSCOPIC CHOLECYSTECTOMY

Brief summary

For patients with symptomatic cholelithiasis, laparoscopic cholecystectomy (LC) is a customary procedure for treatment these days. After LC, patients may experience considerable pain. This study was performed with the objective of comparing the mean duration of analgesia of intraperitoneal bupivacaine with dexmedetomidine to intraperitoneal bupivacaine alone in patients undergoing laparoscopic cholecystectomy.

Interventions

DRUGBupivacaine injection

patients received intraperitoneal bupivacaine 50 ml 0.25% + 5 ml normal saline.

DRUGDexmedetomidine injection

Patients were given intraperitoneal bupivacaine 50 ml 0.25% + dexmedetomidine 1 μg/kg with normal saline 5 ml.

Sponsors

Bahawal Victoria Hospital
CollaboratorUNKNOWN
RESnTEC, Institute of Research
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients of either gender * Aged between 20 and 70 years * ASA (American Society of Anesthesiologists Classification) physical status I and II * Undergoing Laparoscopic Cholecystectomy under general anesthesia

Exclusion criteria

* Patients sensitive to local anesthetics * Patients with acute cholecystitis, choledocholithiasis, or ascending cholangitis (temperature≥38.6°C, serum bilirubin≥1.2mg/dl, and ultrasound showing common bile duct diameter of ≥1cm). * Patients with uncontrolled diabetes (FBS≥110 mg/dl) * Uncontrolled blood pressure (SBP≥140 mmHg) * Ischemic heart disease (EF≤40%) * Pulmonary dysfunction (FEV≤70 percent of normal)

Design outcomes

Primary

MeasureTime frameDescription
Duration of analgesia24 hoursThe duration of postoperative analgesia was calculated as the time in minutes starting after the dressing of the patient in the operation room until the patient had a VAS≥3.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026