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Effect of Intranasal Midazolam Versus Ketamine Midazolam Combination as a Premedication on the Occurrence of Postoperative Respiratory Adverse Events

Phase 3
Completed
Conditions
Tonsillectomy
Adenoidectomy
Drug-Related Side Effects and Adverse Reaction
Interventions
Registration Number
NCT06122948
Lead Sponsor
Kasr El Aini Hospital
Brief Summary

The aim of this study is to investigate the effect of addition of intranasal ketamine to midazolam compared to midazolam alone as a premedication on the occurrence of PRAEs

Detailed Description

Perioperative respiratory adverse events (PRAEs) are the most common complication during pediatric anesthesia furthermore, most children presenting for AT have sleep-disordered breathing and obstructive sleep apnea syndrome (OSAS) caused by tonsillar hypertrophy which could aggravate the PRAEs specially with the use of the conventional sedatives as a premedication. A recent randomized controlled trial has shown that more than 50% of children premedicated with midazolam had experienced PRAEs . Midazolam and ketamine are commonly used as preoperative sedative drugs for pediatric populations. Ketamine is a safe and widely used sedative and analgesic in the pediatric emergency department (ED) with less profound effects on the upper airway and respiratory muscles. Intranasal ketamine administration is well tolerated and without serious adverse effects. The addition of ketamine to midazolam as a preoperative sedation to reduce the occurrence of PRAEs was not investigated before in children undergoing AT. The authors hypothesize that combination of ketamine to midazolam could offer optimum sedation condition while reducing the occurrence of PRAEs in children undergoing AT.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
200
Inclusion Criteria
  • Children both sexes male and female.
  • Age from 3 to 12 years old.
  • ASA grade I, II.
  • undergoing elective AT procedures.
Exclusion Criteria
  • Congenital heart diseases (cyanotic and a cyanotic).
  • Congenital syndromes affecting airway anatomy such as Pierre-Robin syndrome and Down syndrome.
  • Severe lung diseases affecting either lung tissue such as pulmonary cystic fibrosis and idiopathic pulmonary fibrosis or affecting lung circulation such as pulmonary hypertension with marked limitation of Physical activity or inability to carry out any physical activity according to NHYA classification.
  • Recent upper respiratory tract infection (less than two weeks).
  • Neuromuscular diseases including cerebral palsy and epilepsy.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
(Group M)The midazolam groupThe midazolam group will receive intranasal midazolam (0.1 mg/kg)
(Group MK)The midazolam ketamine groupMidazolam ketamine group will receive intranasal midazolam (0.1mg/kg) and ketamine (3mg/kg)
Primary Outcome Measures
NameTimeMethod
The incidence of any perioperative respiratory adverse events (PRAEs)8 hours

the incidence of any PRAEs (Perioperative respiratory adverse events (PRAEs) which are manifested as minor (oxygen desaturation (SaO2 less than 95% for 10 seconds) or coughing) and major as (bronchospasm, laryngospasm, airway obstruction, stridor or hypoxia (oxygen desaturation less than 90%)) among midazolam versus midazolam ketamine groups.

Secondary Outcome Measures
NameTimeMethod
Postoperative pain score8 hours

• Postoperative pain score using (Wong-Baker Pain Scale)

Sedation success rate8 hours

• Sedation success rate (score of 3 or 4 is considered successful sedation) using Funk score

Postoperative emergence delirium8 hours

• Postoperative emergence delirium, a total Postoperative emergence delirium PAED score≥ 10 will be considered indicative of the presence of ED using (PAED scale

Trial Locations

Locations (1)

Cairo university hospitals, kasralainy

🇪🇬

Cairo, Egypt

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