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Impact of Anaesthesiology Management on Paediatric Emergence Delirium Incidence

Anaesthesiology Management and the Impact on Emergenece Delirium Incidence in Paediatric Patients Undergoing Adenoidectomy or Adenoidectomy With Frenulum Dicsision a/or Microotoscopy: Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04291820
Acronym
AnaPed
Enrollment
300
Registered
2020-03-02
Start date
2023-09-01
Completion date
2023-12-31
Last updated
2023-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emergence Delirium

Keywords

Delirium, Emergence delirium, Paediatric patient, Anaesthesia

Brief summary

Postoperative emergence delirium (ED) is a severe postoperative complication in paediatric anaesthesia. ED is defined as a state with psychomotor disturbance, perception disorder and state of excitation and anxiety. The incidence of ED in paediatric patients can be up to 80%. ED is associated with the increased morbidity of paediatric patients in the postoperative period. One of the potential triggers of ED is sevoflurane. Currently, there are only limited data about comparing the influence of anesthesiologic management on the ED incidence. The possible ED reduction could lead to reduced stay in a post-anaesthesia care unit (PACU), postoperative nausea and vomiting (PONV) incidence and the overall reduction of the postoperative adverse events incidence together with the higher satisfaction and the patients and the legal guardians.

Detailed description

This prospective randomized interventional single-blind study aims to compare the influence of the anaesthesiology management no the incidence of ED in the postoperative period in paediatric patients. Elective paediatric patients (2-10 years) scheduled for the planned adenoidectomy or adenoidectomy + micro-otoscopy/adenoidectomy + frenulum linguae discission will be included in the trial after signed informed consent form the legal guardian. In all patients, the 2 Eutectic Mixture of Local Anesthetics (EMLA) patch will be applied on the predefined skin area ( visible vein for venepuncture) between 45 minutes to 60 minutes before anaesthesia. The patients will be randomized at the operating theatre (allocation 1:1) into the experimental group (intravenous induction with propofol + opioid and anaesthesia maintenance according to this set bispectral index value with desflurane) and the control group (inhalation induction with sevoflurane mixed with air and oxygen and anaesthesia maintenance with sevoflurane). The primary aim of the study will be the incidence of ED defined by The Pediatric Anesthesia Emergence Delirium (PAED) scale, which will be measured at the , at the admission to PACU and in the 5th, 10th, 15th, 30th minute and at the moment of dismission from PACU. The secondary aim will be the time to oral intake (from the end of the surgery), the incidence of adverse events (PONV, bradycardia, hypotension), the need for concomitant medication (analgesic medication, sedative medication, antiemetic medication).

Interventions

PROCEDUREIntravenous induction and desflurane anaesthesia maintenance

Anaesthesia will be inducted with intravenous propofol + opioid and maintained with desflurane according to the BIS levels

PROCEDUREInhalation induction with sevoflurane and anaesthesia maintenance with sevoflurane

Anaesthesia will be inducted with sevoflurane and maintained with sevoflurane according to the BIS levels

Sponsors

Brno University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Masking description

The participants will be blinded by the arm inclusion. The outcomes will be measured by the blinded nurse in the PACU

Intervention model description

A prospective interventional single-blind randomized trial

Eligibility

Sex/Gender
ALL
Age
2 Years to 10 Years
Healthy volunteers
No

Inclusion criteria

* age between 2-10 years * signed informed consent * paediatric patient for elective adenoidectomy, or adenoidectomy with micro-otoscopy and/or frenulum discission

Exclusion criteria

* allergy and hypersensitivity on local anaesthetics in EMLA patch, general anaesthetics, or soya beans or peanuts * venepuncture refusal · neuromuscular disorder with the contraindication of inhalation anaesthetics

Design outcomes

Primary

MeasureTime frameDescription
Emergence delirium incidencepostoperative period, up to 1 hour postoperativelyThe incidence of emergence delirium based on PAED score

Secondary

MeasureTime frameDescription
Time to first oral intakepostoperative period, up to 1 hour postoperativelyThe interval between the end of surgery and first oral intake will be measured
Adverse events incidencepostoperative period, up to 1 hour postoperativelyThe adverse events in the postoperative period will be evaluated - postoperative nausea and vomiting, bradycardia, hypotension, anxiety
The need for concomitant medication in PACUpostoperative period, up to 1 hour postoperativelyThe need for concomitant medication in PACU - analgesic, sedative, antiemetic medication

Countries

Czechia

Contacts

Primary ContactPetr Stourac, assoc.Prof.MD.Ph.D
stourac.petr@fnbrno.cz5 3223 4261
Backup ContactJozef Klučka, MD
Klucka.jozef@fnbrno.cz532234696

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026