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Study the safety of fentanyl+propofol vs Dexmedetomidine and Ketamine+Propofol as a including agent in general anesthesia for laproscopic cholecystectomy:Randomized clinical study

Study the safety of fentanyl + propofol Vs Dexmedetomidine and Ketamine + propofol as a inducing agent in general anesthesia for laparoscopic cholecystectomy Randomized clinical study - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/098252
Enrollment
34
Registered
2025-12-01
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

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: Dexmedetomidine and ketamine + propofol a inducing agent: Dexmedetomidine maintaince as per kg ketamine 0.3 mg/kg propofol 2mg/kg Intervention2: safety of fentanyl + propofol: fentanyl-

Sponsors

D Y Patil University School of Medicine and Hospital Nerul Navi Mumbai
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: INCLUSION CRITERIA a. All patients undergoing elective laproscopic cholecystectomy b. (BMI) of 18-35 kg/m2 c. ASA grade I and II. d. Age group 18-60 years

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
To compare incidence of post operative nausea vomiting in first 12 hours in both groupsTimepoint: To compare incidence of post operative nausea vomiting in first 12 hours in both groups

Secondary

MeasureTime frame
To compare Hemodynamic response at the time of induction to pneumoperitoneum that is 5-10 MINS in both groupsTimepoint: 5-10 MINS

Countries

India

Contacts

Public ContactDr Mona Jadhav

padmashree d y patil school of medicine navi mumbai

monajadhav601@hotmail.com09763847148

Outcome results

None listed

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