Skip to content

Evaluation of ketamine in managing post operative pain following laproscopic cholecystectomy

Efficacy of ketamine for acute and chronic post operative analgesia in laproscopic cholecystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/10/037604
Enrollment
50
Registered
2021-10-27
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: Ketamine: 0.5ml/kg diluted to 2 ml with normal saline given intravenous 15 minutes prior to surgical incision Control Intervention1: Normal saline: 2 ml normal saline given intravenous

Sponsors

SMSR Sharda University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I and II patients of either sex, between 20-60 yrs of age, undergoing elective laparoscopic cholecystectomy under general anesthesia,

Exclusion criteria

Exclusion criteria: The patients unable to understand NRS, allergic to local anesthetics, had chronic pain disease other than gall stone disease, choledocholithiasis, acute pancreatitis, or were pregnant, were excluded from the study. Whenever surgical procedure necessitated the conversion of laproscopic cholysectomy to open procedure, such patients was also excluded from the study.

Design outcomes

Primary

MeasureTime frame
The length of time between extubation and the first request for pain medication was recorded. Chronic pain (NRS score)will be asked from the patient every 15 days on telephone till 6 months.Timepoint: The length of time between extubation and the first request for pain medication was recorded. Chronic pain will be asked from the patient every 15 days on telephone till 6 months post surgery.

Secondary

MeasureTime frame
shoulder pain, nausea, vomiting were also recorded.Timepoint: 24 hours;The total and cumulative consumption of analgesics (tramadol) will be recorded after 24 hours.Timepoint: 24 hours

Countries

India

Contacts

Public ContactShruti Jain

School of Medical Sciences and Research

shruti.anaesth@gmail.com01204570424

Outcome results

None listed

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