CTRI/2020/10/028554Not yet recruitingNot Applicable
Does the addition of caudal analgesia warrant dextrose supplementation in pediatric abdominal surgery?
Amrita Institute of Medical Sciences1 site in 1 country50 target enrollmentStarted: October 30, 2020Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Enrollment
- 50
- Locations
- 1
- Primary Endpoint
- Blood sugars meausured half hourly during surgery with and without supplemental glucose in children receiving caudal analgesia undergoing abdominal surgery
Study Overview
Brief Summary
Regional anesthesia obtunds tress responses to surgery and anesthesia. We propose to evaluate the blood sugar profiles amongst children undergoing abdominal surgery with caudal analgesia with and without dextrose supplementation with a view to document the safety of withholding dextrose containing solutions in children undergoing surgery.
Study Design
- Study Type
- Interventional
- Allocation
- Random Number Table
- Masking
- Not Applicable
Eligibility Criteria
- Ages
- 6.00 Month(s) to 6.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •1.Age 6 months.
- •6 years 2.Surgery ≥ 1hour 3.Fasting for 6 hours for solid food and formula feeds, 4 hours for breast milk, 2 hours for glucose-containing fluids.
Exclusion Criteria
- •1.ASA physical status ≥2 2.Patients diagnosed with endocrine disorders/ on steroid supplementation.
Outcomes
Primary Outcomes
Blood sugars meausured half hourly during surgery with and without supplemental glucose in children receiving caudal analgesia undergoing abdominal surgery
Time Frame: 1. Baseline R0 | 2. 30 minutes R 30 | 3. 60 minutes R 60 | 4. 90 mintes R 90 | 5. End of surgery R final.
Secondary Outcomes
- Hemodynamic changes , hear rate and blood pressure at the same time points.(Opioid consumption during surgery)
Investigators
Study Sites (1)
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