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comparative study between ketofol and propofol as an induction agent;a hemodynamic study profile in patients undergoing laparoscopic surgery under general anesthesia

COMPARATIVE STUDY BETWEEN PROPOFOL AND KETOFOL(KETAMINE +PROPOFOL)AS AN INDUCTION AGENT- A STUDY OF HEMODYNAMIC PROFILE IN PATIENTS UNDERGOING LAPAROSCOPIC SURGERY UNDER GENERAL ANAESTHESIA - CPKH

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/10/021607
Enrollment
80
Registered
2019-10-11
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: ketofol: better hemodynamic stability Control Intervention1: propofol: hemodynamic instability

Sponsors

pondicherry institute of medical sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. All patients between 18-50 yrs of age undergoing laparoscopic surgeries 2.â??ASAI(American Society of Anaesthesiologists I ) or ASA II (American Society of Anaesthesiologists II ) of either sex

Exclusion criteria

Exclusion criteria: 1.Any known contra indication or a allergy to the study drug 2.Emergency surgeries 3.History of alcoholic abuse, patients with psychiatric illness 4.Patients who are known hypertensive 5.Uncontrolled diabetic mellitus, cardiac disorders 6.Pregnant patients 6.Obese Patients (BMI >30kg/m2)

Design outcomes

Primary

MeasureTime frame
TO COMPARE THE EFFECT OF PROPOFOL AND KETOFOL AS AN INDUCTION AGENT A HEMODYNAMIC PROFILE IN PATIENT UNDERGOING LAPROSCOPIC SURGERYTimepoint: FROM INDUCTION TO PNEUMO-PERITONEUM—

Secondary

MeasureTime frame
1To study and compare the recovery profile from the anaesthesia between the two groups (from the time of stopping inhalation agents to eye opening ) 2.To study the incidence of post operative nausea and vomiting between two groups 3. To study the Incidence of post operative shivering between two groups 4.To record the occurrence of complications like hallucination ,vivid dreams and confusion, if any post operatively Timepoint: 1To study and compare the recovery profile from the anaesthesia between the two groups (from the time of stopping inhalation agents to eye opening ) 2.To study the incidence of post operative nausea and vomiting between two groups 3. To study the Incidence of post operative shivering between two groups 4.To record the occurrence of complications like hallucination ,vivid dreams and confusion, if any post operatively—

Countries

India

Contacts

Public ContactVIKASINI

pondicherry institute of medical sciences

koshysm@yahoo.com9443287707

Outcome results

None listed

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