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Clinical Trials/NCT04704622
NCT04704622
Completed
Phase 2

Comparative Evaluation of Intranasal Midazolam, Dexmedetomidine, Ketamine for Their Sedative Effect and the Ability to Facilitate Venous Cannulation in Pediatric Patients: a Prospective Randomized Study.

Ain Shams University1 site in 1 country150 target enrollmentJanuary 1, 2021

Overview

Phase
Phase 2
Intervention
Dexmedetomidine
Conditions
Cannula Site Pain
Sponsor
Ain Shams University
Enrollment
150
Locations
1
Primary Endpoint
the change of Modified Observer Assessment of Alertness and Sedation scale(MOAA/S) at different time intervals
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Background and Objectives: Surgery and hospitalization present a very stressful period for children and their parents. The induction of anesthesia and cannula insertion may be the only bad experience a child can remember during his procedure. Pediatric intravenous cannulation is technically difficult and moreover may cause psychological problems. Sedative Premedication has a great role in pediatric anesthesia to overcome fear and anxiety and to facilitate easy separation from their parents. Intranasal approach is safe and painless and well tolerated by children in addition to a comparable onset of action with the intravenous approach. Midazolam, dexmedetomidine and ketamine have proved their effectiveness as a sedative premedication. The objective of the current study was to compare the effectiveness of administration of intranasal midazolam, dexmedetomidine and ketamine as sedatives to facilitate and decrease the discomfort of intravenous cannulation before surgery in children undergoing various surgical procedures. Methods: the patients agreed to participate in the research were classified into 3 groups. Dexmedetomidine, Midazolam and Ketamine group; each group received the intranasal drug 30 min before the procedure. Pulse, MAP, oxygen saturation and sedation score (MOAA/S) baseline and every 10 min. Easiness of venipuncture, parental separation and any complication encountered were recorded.

Detailed Description

Background and Objectives: Surgery and hospitalization present a very stressful period for children and their parents. The induction of anesthesia and cannula insertion may be the only bad experience a child can remember during his procedure. Pediatric intravenous cannulation is technically difficult and moreover may cause psychological problems. Sedative Premedication has a great role in pediatric anesthesia to overcome fear and anxiety and to facilitate easy separation from their parents. Intranasal approach is safe and painless and well tolerated by children in addition to a comparable onset of action with the intravenous approach. Midazolam, dexmedetomidine and ketamine have proved their effectiveness as a sedative premedication. We assumed that intranasal midazolam, dexmedetomidine and ketamine would help anesthetics to carry out venous cannulation easily; in addition to their sedative premedication effect. The objective of the current study was to compare the effectiveness of administration of intranasal midazolam, dexmedetomidine and ketamine as sedatives to facilitate and decrease the discomfort of intravenous cannulation before surgery in children undergoing various surgical procedures. Study design: 150 patients agreed to participate in the research after written informed consent. patients were classified into 3 groups. Dexmedetomidine, Midazolam and Ketamine group; each group received the intranasal drug 30 min before the procedure. Pulse, MAP, oxygen saturation and sedation score (MOAA/S) baseline and every 10 min. Easiness of venipuncture, parental separation and any complication encountered were recorded. Group assignment, preparation and administration of drugs will be performed by a junior anesthetist who is neither involved nor interested by any means in the study.

Registry
clinicaltrials.gov
Start Date
January 1, 2021
End Date
February 15, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Rasha Gamal Abusinna

lecturer of anesthesia and intensive care, Principal Investigator

Ain Shams University

Eligibility Criteria

Inclusion Criteria

  • all the following must be included
  • child aged between 2-9 years scheduled for minor elective surgical procedures (last 1-2 hours) at pediatric surgery department.
  • Patients were ASA I or II.
  • within normal range of weight.
  • refusing venous cannulation

Exclusion Criteria

  • any of the following
  • parents' refusal
  • with nasal deformity or pathology
  • any known case of allergy to the study drugs
  • obese patients
  • suspected difficult airway or venous cannulation.
  • maxillofacial malformations
  • gastroesophageal reflux
  • patients with renal, liver, endocrine or cardiac pathology
  • patients with increased intracranial or intraocular pressure

Arms & Interventions

dexmedetomidine group

dexmedetomidine intranasal injection,1 μg/kg, once, 30 min preoperative

Intervention: Dexmedetomidine

ketamine

ketamine intranasal injection,2 mg/kg, once, 30 min preoperative

Intervention: Ketamine

midazolam

midazolam intranasal injection,0.2 mg/kg, once, 30 min preoperative

Intervention: Midazolam

Outcomes

Primary Outcomes

the change of Modified Observer Assessment of Alertness and Sedation scale(MOAA/S) at different time intervals

Time Frame: measuring the Modified Observer Assessment of Alertness and Sedation scale every 10 minutes preoperative till induction of anesthesia up to 30 minutes

scale measuring level of sedation from 1-6 points. 1 is referring to no sedation and 6 is the maximum sedation. reaching score of 4 is the sedation level needed to insert the cannula.

Secondary Outcomes

  • the change in measuring pulse rate/ minutes at different time intervals(the recorded score at baseline and every 10 minutes preoperative till induction of anesthesia and intraoperative in a surgery 1-2 hours)
  • the change in Mean Arterial Pressure at different time intervals(the recorded score at baseline and every 10 minutes preoperative till induction of anesthesia and intraoperative in a surgery 1-2 hours)
  • the change in oxygen saturation at different time intervals(the recorded score at baseline and every 10 minutes preoperative till induction of anesthesia and intraoperative in a surgery 1-2 hours)
  • the ease of venipuncture score(done by the anesthetist immediately after the cannula insertion)

Study Sites (1)

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