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Comparision of ondansetron and lignocaine for reduction of pain during propofol intravenous injection in adult patient undergoing laparoscopic cholecystectomy.

Comparision of lignocaine and ondansetron for attenuation of propofol induced pain in adult patient undergoing laparoscopic cholecystectomy.

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/08/020559
Enrollment
100
Registered
2019-08-05
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: K80- Cholelithiasis

Interventions

Control Intervention1: Injection Lignocaine 20% intravenous: administrated 1 minute prior to propofol injection under venous statis at the site of injection of 30-40 mmofHg. Control Intervention2: Inj

Sponsors

PGIMER and Dr RML Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA Grade I and II patients. 2.Patients of either sex, aged 18yrs and above. 3.Patient scheduled for various elective surgical procedures under general anesthesia.

Exclusion criteria

Exclusion criteria: 1.Patients belonging to ASA 3 and 4. 2.Patients with known cardiac disorders, other systemic disorders of lungs and liver. 3.Pregnant patients. 4.Patients for emergency procedures. 5.Patient allergic to propofol, lignocaine or ondansetron. 6.Patient with history of motion sickness, history of PONV, on nasogastric tube and patients with difficult airway.

Design outcomes

Primary

MeasureTime frame
Attenuation of Propofol induced pain by lignocaine and ondansetron in adult patient undergoing laparoscopic cholecystectomy.Timepoint: with in 20 seconds of propofol injection

Secondary

MeasureTime frame
Post- operative incidence of nausea and vomiting in two groupsTimepoint: up-till 2 hours post-surgery

Countries

India

Contacts

Public ContactAkash Kanojia

PGIMER and Dr R.M.L Hospital

drsoodrajesh@gmail.com9810218916

Outcome results

None listed

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