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Observation of effect of dexmedetomidine when given intravenously to the pediatric patients undergoing levobupivacaine spinal anaesthesia.

Not Applicable
Completed
Conditions
Health Condition 1: null- good health.
Registration Number
CTRI/2017/12/010744
Lead Sponsor
Department of anaesthesia
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
70
Inclusion Criteria

1) class-1 and class-2 patients

2) lower abdominal surgery

3) 2 year to 12 year age

Exclusion Criteria

1) patients refusal.

2) contraindication for spinal anaesthesia

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Intravenous dexmedetomidine prolong the effect of bupivacaine spinal anaesthesiaTimepoint: end of clinical trial
Secondary Outcome Measures
NameTimeMethod
provide haemodynamic stability. <br/ ><br>provide good intraoperative sedation and pain free period during operation and postoperative periodTimepoint: end of clinical trial
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