A clinical trial to study the effect of changes in the strength of pulse to predict the onset of caudal block which is a method of giving pain relief in childre
Not Applicable
- Conditions
- Health Condition 1: N430- Encysted hydroceleHealth Condition 2: N433- Hydrocele, unspecifiedHealth Condition 3: O- Medical and SurgicalHealth Condition 4: N472- ParaphimosisHealth Condition 5: N471- Phimosis
- Registration Number
- CTRI/2021/06/034021
- Lead Sponsor
- Institute of Anaesthesiology and Critical care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To monitor perfusion index after caudal block at regular time intervals at T0,T3,T5,T10,T15,T20,T30Timepoint: Baseline,3min,5min,10min,15min,20min,30min and hourly till 6 hours in the recovery room
- Secondary Outcome Measures
Name Time Method Patient Hemodynamic parametersTimepoint: Perioperative period