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Effect of analgesia on postoperative delirium

Not Applicable
Conditions
Health Condition 1: I39- Endocarditis and heart valve disorders in diseases classified elsewhereHealth Condition 2: null- Paeditric patients who require surgery under general anaesthesia
Registration Number
CTRI/2018/07/014993
Lead Sponsor
Intramural funding by Research cell
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

undergoing elective infra-umbilical surgery over period of 6 months will be enrolled

Exclusion Criteria

Emergency surgery, patients with systemic illness, coagulation disorders, cognitive impairment or communication disorders, known allergy to any of the drugs used in the study protocol and concurrent treatment with analgesic or anticonvulsant drugs will be excluded from study.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Primary objective is to evaluate effect of quality of analgesia, measured as pain scores, on incidence of emergence delirium.Timepoint: during extubation and at 5 min, at 10 min, at 15min and at 20 min
Secondary Outcome Measures
NameTimeMethod
2.Secondary objective is to determine effect of postoperative caudal analgesia on incidence of ED.Timepoint: during extubation and at 5 min, at 10 min, at 15min and at 20 min
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