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checking the effect of fentanyl after giving two doses of injection dexmedetomidine before surgery in patients undergoing laparoscopic cholecystectomy

comparison of total intraoperative rescue fentanyl consumption after two different doses of preoperative intravenous dexmedetomidine in laparoscopic cholecystectomy - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061310
Enrollment
75
Registered
2024-01-09
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: K800- Calculus of gallbladder with acutecholecystitis Health Condition 2: K802- Calculus of gallbladder without cholecystitis

Interventions

Intervention1: Administration of two diiferent doses of dexmedetomidine intervenously: preoperative administration of two different doses intravenous dexmedetomidine for patients undergoing laparoscop

Sponsors

Department of Anaesthesia and Intensive Care
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA physical status I and II of either sex 2. Age between 18 to 65 years 3. BMI =20 to=35 kg m2 4. Scheduled for laparoscopic cholecystectomy surgery

Exclusion criteria

Exclusion criteria: 1. Refusal by the patient 2. Patient with coagulopathy and bleeding disorder 3. Pregnant or lactating women 4. Contraindications or allergy to dexmedetomidine and fentanyl 5. Patient having hemodynamic instability. 6. Patients having pain in any area other than surgery site

Design outcomes

Primary

MeasureTime frame
Total intraoperative rescue dose of fentanyl consumed.Timepoint: 0, 5, 15mins before induction, at the time of intubation and every 10 minutes after intubation till the end of surgery

Secondary

MeasureTime frame
1. Haemodynamic response at 0, 5, 15mins before induction, at the time of intubation and every 10 minutes after intubation till the end of surgery. 2. Total induction dose of propofol consumed. 3. Post-operative VAS score at patient arrival at PACU, 5, 10, 15, 30 minutes 1, 3, 6, 12 and 24 hours. 4. Time to first rescue analgesia postoperatively. 5. Adverse effects if any. Timepoint: 0 minutes, 5 minutes, 10 minutes, 15 minutes, 30 minutes, 1 hour, 3 hours, 6 hours, 12 hours, 24 hours

Countries

India

Contacts

Public ContactDr Deepak Thapa

Government Medical College and Hospital

dpkthapa@gmail.com9646121524

Outcome results

None listed

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