Reduction of pain due to propofol by ondansetron or lignocaine - a comparative study

Phase 4

• Conditions: Health Condition 1: null- Pain due to propofol administration

• Registration Number: CTRI/2018/05/013827
• Lead Sponsor: Sri Devaraj Urs Academy of Higher Education and Research

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1.Patients of either gender aged between 21- 50 years

2.Patients with body weight of 50-80 Kg

3.Patients undergoing elective surgeryunder general anesthesia

4.Patients belonging to American Society of Anesthesiology (ASA) physical status I and II

Exclusion Criteria

1.History of allergy to study drugs

2.Pregnant and lactating women

3.Patients receiving analgesics 48 hours before surgery

4.Patients with pain posted for elective surgery

Study & Design

• Study Type: Interventional
• Study Design: Not specified