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A clinical based study to find out the exact lowest possible dose of ketamine, a drug which takes care of the pain and also helps in maintaining the state of anaesthesia during surgery, in keeping the patient pain free in the period after Laparoscopic Cholecystectomy surgery.

A Parallel Group, Double-Blind, Randomized Controlled Trial to assess the optimum dose of ketamine infusion in management of early postoperative pain in Elective Laparoscopic Cholecystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/01/022983
Enrollment
140
Registered
2020-01-27
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

Health Condition 1: K802- Calculus of gallbladder without cholecystitis

Interventions

Intervention1: Patients undergoing elective laparoscopic cholecystectomy will be allotted into 3 subgroups with 35 patients each and will recieve 20 mcg/kg/min (Group K1), 30 mcg/kg/min (Group K2) & 4

Sponsors

Midnapore Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Age group between 18-65 years. 2) ASA grade I to II. 3) Patients posted for Elective laproscopic cholecystectomy under General

Exclusion criteria

Exclusion criteria: 1) Psychiatric disorders such as schizophrenia and acute psychoses. 2) Patients with features of raised IntraCranial Pressure 3) Penetrating Eye injury and increased IntraOcular Pressure. 4) Regular use of anti-inflammatory drugs (NSAIDs) 5) Chronic pain syndromes 6) Acute or chronic alcohol intoxication 7) Chronic kidney disease, Chronic Liver disease 8) Moderate to severe hypertension 9) Acute Porphyria 10) History of CErebroVascular accident 11) Intolerance or allergy to S(+)-ketamine 12) Any patients below 18 years old and above 65 years old 13) Any drug allergy. 14) Any emergency surgery.

Design outcomes

Primary

MeasureTime frame
1. To assess the effectiveness of different doses of intraoperative ketamine infusion for post operative analgesia in reducing the need for rescue analgesic requirement. 2.To assess the time of requirement of first rescue analgesic dose in each individual groups.Timepoint: During the period of next 24 hours following the surgery

Secondary

MeasureTime frame
observation of change in hemodyanamic profile in either groups upon administering of the test drugTimepoint: throughout the surgery duration

Countries

India

Contacts

Public ContactBani Parvati Magda Hembrom

Dept. of Anaesthesiology, Midnapore Medical College

banihembrom72@gmail.com9903207690

Outcome results

None listed

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