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Effect of Intravenous Low-Dose Ketamine Infusion With Intravenous Lignocaine Infusion on Post-Operative Pain in Patients Undergoing Laparoscopic Choleysystectomy Under General Anesthesia

Effect of Intravenous Low-Dose Ketamine Infusion With Intravenous Lignocaine Infusion on Post-Operative Pain in Patients Undergoing Laparoscopic Choleysystectomy Under General Anesthesia

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06964555
Enrollment
100
Registered
2025-05-09
Start date
2024-01-01
Completion date
2024-12-31
Last updated
2025-05-22

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

Conditions

Cholelithiases

Keywords

Cholelithiases, Cholecystectomy, Laparoscopy

Brief summary

Objective: To determine the effect of low-dose ketamine versus lignocaine on post-operative pain in patients undergoing LC under general anesthesia in a tertiary care hospital. Sample Selection: Patients of both the gender of age at least 18 years, planned for elective LC with ASA grade I-II were included. Patients with obesity, history of alcohol consumptions, drug abusers, uncontrolled hypertension and diabetics, with chronic pain, allergic to study drugs, having neurological disorders, unable to understand pain scoring system and converted to open LC were excluded.

Interventions

Ketamine group received ketamine at 0.2mg/kg bolus intravenously followed by ketamine infusion at rate of 0.2mg/kg/hr throughout the surgery.

IV Lignocaine was given at the rate of 1 mg/kg/hr.

Sponsors

Fazaia Ruth Pfau Medical College
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients of both the gender of age at least 18 years * Patients planned for elective LC * Patients with ASA grade I-II were included.

Exclusion criteria

* Patients with obesity, * Patients with history of alcohol consumptions, uncontrolled hypertension and diabetics, * Drug abusers * Patients with chronic pain * Patients allergic to study drugs * Patients having neurological disorders or unable to understand pain scoring system * Patients converted to open LC

Design outcomes

Primary

MeasureTime frameDescription
Post operative Pain24 hoursPain was assessed using Numeric Rating Scale which is a ten point scoring scale ranging from 0-10 for ranking pain where 0 means no and 10 means worst pain.

Secondary

MeasureTime frameDescription
Time to rescue analgesia24 hoursTime to rescue analgesia was defined as time point at which patient will be given first rescue analgesia for pain of score more 5 or above.
Wound ClosureEnd of SurgeryThe time between the incision and the wound's closure was used to define the length of the surgery.

Countries

Pakistan

Outcome results

None listed

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