Skip to main content
OpenTrials
Completed

NCT Number: NCT03220880

Intranasal Dexmedetomidine Sedation in Children for Non-painful Procedures

Specific Aim 1: To describe the adequacy of sedation associated with different regimens of IN DEX in children undergoing non-painful procedures. This aim will test the working hypothesis that IN DEX regimens are effective for producing sedation adequate for completion of non-painful procedures in children.

Specific Aim 2: To describe the temporal characteristics associated with varied regimens of IN DEX in children undergoing non-painful procedures, such as time to onset of adequate sedation; time to procedure start; and time from procedure end to meeting discharge criteria. This aim will test the working hypothesis that IN DEX regimens have temporal characteristics that are favourable for sedating children for non-painful procedures.

Specific Aim 3: To describe the adverse events associated with varied regimens of IN DEX in children undergoing non-painful procedures. This aim will test the working hypothesis that IN DEX regimens have a low incidence of adverse events.

Completed

Looking for future studies?

Notify Me

Key information

Age range

2 month–17 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Santa Clara Valley Medical Center, San Jose, California, United States

Loading trial locations.

About this study

Dexmedetomidine (DEX) is an alpha-2 receptor agonist with sedative, anxiolytic, and analgesics properties. DEX has been used extensively for sedation in children to facilitate different non-painful procedures, such magnetic resonance imaging (MRI), auditory brainstem response (ABR) tests, and computed tomography (CT) scans. In particular, DEX can be administered by the intranasal (IN) route. Intranasal administration has the benefits of being both effective and needle-free, of which the latter makes it less distressing to children compared to sedatives administered by the intravenous (IV) route. There is a gap of knowledge, however, regarding the ideal regimen of IN DEX for providing optimal procedural sedation in children undergoing non-painful procedures. There is a large variation in practice using IN DEX, both regarding the dose and the use of adjunct medications. It is also unknown whether regimens should vary based on patient factors such as age. There is no clear evidence to define best practice when using IN DEX to provide sedation in this population to achieve the desired outcomes most relevant to clinicians. The rationale of the proposed investigation is that by conducting an exploratory study to measure clinical outcomes associated with IN DEX, the investigators can begin to identify trends and differences that will lay the foundation for randomized clinical trials to identify the ideal regimen for IN DEX when providing sedation for non-painful procedures. This will then allow the investigators to compare IN DEX, at its best, to other sedatives so that the sedative and regimen associated with the best outcomes relevant to sedation of children undergoing non-painful procedures can be determined.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children 2 months to 17 years (i.e. before their 18th birthday)
  • Child will be receiving intranasal dexmedetomidine as part of their usual medical care
  • Child will be undergoing a non-painful medical procedure, which includes (but is not limited to): MRI, CT scans, ABR/BAER, echocardiograms, and EEGs.

Exclusion criteria

  • Known allergy to dexmedetomidine
  • Known abnormal renal or hepatic function
  • Known cardiac conduction abnormality or heart block
  • Current use of digoxin or beta-blockers

Treatment and study plan

Intranasal dexmedetomidine

Drug

Intranasal dexemedetomidine (100 mcg/mL), 0.5 to 4 mcg/kg

Primary outcomes

  1. Adequacy of sedation

    Time frame: 1 hour

    Pediatric Sedation State Scale

Secondary outcomes

  1. Time to onset of adequate sedation

    Time frame: 1 hour

    Time in minutes after administration of IN DEX to achieve a University of Michigan Sedation Scale (UMSS) score of 3 or more

  2. Time to discharge

    Time frame: 2 hours

    Time in minutes after procedure end to achieving Modified Aldrete Scoring System (MASS) score of 9 or greater, or baseline MASS score.

Other outcomes

  1. Adverse events

    Time frame: 3 hours

    Adverse events and/or required interventions (e.g. cardiovascular, airway) required

Sponsors and collaborators

Lead sponsor

Columbia University

Other

Collaborators

  • Baylor College of Medicine
  • Boston Children's Hospital
  • Children's Healthcare of Atlanta
  • Children's Hospital Medical Center, Cincinnati
  • HSHS St. John's Hospital
  • Santa Clara Valley Medical Center
  • UNC Children's Hospital
  • University of Pittsburgh

Registry information

Official study title

Clinical Characteristics of Intranasal Dexmedetomidine for Sedation in Children Undergoing Non-painful Procedures

Important dates

Study start
2018
Primary completion
2020
Study completion
2020
First posted
Jul 18, 2017
Registry last updated
Sep 10, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.