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Comparing the effects of intravenous Lignocaine and Ketamine on postoperative pain after Ear, Nose and Throat surgeries.

Phase 3
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/08/055969
Lead Sponsor
Dr Megha M Rao
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

ASA class I and II

Exclusion Criteria

Patients requiring postoperative mechanical ventilation or regional analgesia

Patients on perioperative gabapentin, magnesium

Pregnant or breastfeeding mothers

BMI more or equal to 35kh/sq meter

Allergy or contraindications to study medications.

Patients with cardiac, renal or hepatic disease.

Patients with seizure or other neurological disorder.

Patients with chronic preoperative opioid use or substance abuse and history of chronic pain.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain assessed post operativelyTimepoint: Assessment of pain immediately post op, <br/ ><br>1hour, <br/ ><br>6hour, <br/ ><br>12hour and <br/ ><br>24hour.
Secondary Outcome Measures
NameTimeMethod
First & total rescue analgesia (paracetamol) consumedTimepoint: 24 hours post-operatively.
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