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Clinical Trials/CTRI/2021/06/034021
CTRI/2021/06/034021
Not yet recruiting
Not Applicable

A Randomised controlled single blinded clinical trial to evaluate the effectiveness of Perfusion Index as a predictor of successful caudal block in children under 5 years

Institute of Anaesthesiology and Critical care1 site in 1 country60 target enrollmentStarted: October 6, 2021Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Institute of Anaesthesiology and Critical care
Enrollment
60
Locations
1
Primary Endpoint
To monitor perfusion index after caudal block at regular time intervals at T0,T3,T5,T10,T15,T20,T30

Overview

Brief Summary

This study is a randomised controlled single blinded clinical trial to evaluate the effectiveness of Perfusion Index as a predictor of successful caudal block in children under 5 years.Perfusion index is measured at baseline and after caudal block in one group and without caudal block in another group.More than 100% Increase in perfusion index will be considered as onset of successful caudal block

Study Design

Study Type
Interventional
Allocation
Computer generated randomization
Masking
Participant Blinded

Eligibility Criteria

Ages
1.00 Day(s) to 5.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Children under 5 years Elective infraumbilical surgeries ASA PS I.

Exclusion Criteria

  • Parents refusal Allergic to drug Severe cardiovascular, respiratory,renal, neurological, hepatic disease Local infection Bleeding diathesis.

Outcomes

Primary Outcomes

To monitor perfusion index after caudal block at regular time intervals at T0,T3,T5,T10,T15,T20,T30

Time Frame: Baseline,3min,5min,10min,15min,20min,30min and hourly till 6 hours in the recovery room

Secondary Outcomes

  • Patient Hemodynamic parameters(Perioperative period)

Investigators

Sponsor
Institute of Anaesthesiology and Critical care
Sponsor Class
Government medical college

Study Sites (1)

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