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Renal Function During Pediatric Anesthesia

Phase 1
Completed
Conditions
Renal Failure
Anesthesia
Interventions
Registration Number
NCT02571426
Lead Sponsor
Uppsala University
Brief Summary

It is known that volatile anesthesia, such as sevoflurane, retain water and that this appears more pronounced in children. However, the mechanisms for this effect is unknown and it is not clear if the commonly used anesthetic propofol does the same. In this study the investigators want to compare the fluid and electrolyte conserving effects of sevoflurane and propofol in a pediatric setting and also investigate humoral changes induced by these anesthetics.

Detailed Description

Prior studies by the investigators research group have shown water and sodium retention in experimental animals undergoing sevoflurane anesthesia. Preliminary data suggest that this is not as obvious with propofol anesthesia. The investigators aim to study if this difference is present in children.

Subjects are collected from ordinary routine operations of hypospadia. By routine, all boys undergoing this surgery get a sacral blockade and a urine catheter. The children are randomized to either sevoflurane or propofol anesthesia. Before or immediately after induction of anesthesia baseline blood samples are collected for analysis of sodium, potassium, creatinine, osmolality, angiotensin II, arginine-vasopressin and aldosterone. Perioperative fluids are started, a balanced glucose infusion with 132mmol sodium content, covering basal fluid need + 20%. This infusion is continued until the end of the protocol at the ward. At the induction of anesthesia the investigators start measuring urine output every 20th minute. The same blood samples as above are collected again during mid-operation. At the end of anesthesia the investigators collect all the urine and send a sample for urine analysis of sodium, potassium, osmolality and creatinine.

In the postoperative ward the investigators again start collecting urine every 20 minutes for 120 minutes. All urine after 120 minutes are collected, and a sample sent for analysis. After 60 minutes at the postoperative ward, blood samples are again collected for analysis.

In the childrens ward the protocol for the postoperative ward is repeated, with urine collection and sample, as well as blood samples. After 120 minutes the protocol ends.

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
24
Inclusion Criteria
  • Eligible for hypospadia surgery.
Exclusion Criteria
  • American Association of Anesthesiology class above 2
  • Weight above 50 kg or below 10 kg
  • Hypersensitivity towards the anesthetic agents (difficult peanut or soy allergy)
  • Inability for parent to understand study information

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PropofolpropofolContinuous infusion during surgery. Individual dosage.
sevofluraneSevofluraneInhalational anesthetic during surgery. Individual dosage
Primary Outcome Measures
NameTimeMethod
urine output during anesthesia2 hours
Secondary Outcome Measures
NameTimeMethod
urine output postoperatively4 hours
Sodium excretion during anesthesia2 hours
sodium excretion postoperatively4 hours
Changes in aldosterone, angiotensin II, arginine-vasopressin during surgery2 hours

Comparison of blood samples of fluid balance regulatory hormones collected at baseline, during surgery and 1 hour + 3 hours postoperatively

Changes in aldosterone, angiotensin II, arginine-vasopressin postoperatively4 hours

Comparison of blood samples of fluid balance regulatory hormones collected at baseline, during surgery and 1 hour + 3 hours postoperatively

Trial Locations

Locations (1)

Akademiska university hospital

πŸ‡ΈπŸ‡ͺ

Uppsala, Sweden

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