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Clinical Trials in Italy / NCT06794879
Recruiting Observational

Survey for Parental Perception of Procedural Analgosedation in Pediatric Age.

NCT06794879 · tracked via the Priya Life Science Italy tracker
Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Phase
Observational
Started
2024-12-11
Last updated
2025-01-27

Condition(s) studied

AnalgesiaSensation, Hyperalgesic

Study summary

The conduction of this study may provide useful information about how much parents know and understand about procedural sedation, helping to identify any gaps. In addition, expectations and concerns about procedural sedation may be highlighted so that strategies aimed at improving communication by health care personnel can be developed. The results may guide the development of training programs for health care personnel so as to improve the management of procedural sedation and interaction with parents.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Parents of children between the ages of 2 months and 14 years who are afferent to the withdrawal clinic Exclusion Criteria: * None

Primary outcome measure(s)

  • Identify the parent's degree of agreement/disagreement with pediatric procedural analgosedation practices and factors that may influence it — through study completion, an average of 1 year
    The parent's degree of agreement/disagreement with pediatric procedural analgosedation practices and the factors that may influence it will be analyzed by administering a survey

Trial sites (1)

FacilityCityRegionStatus
IRCCS Azienda Ospedaliero - Universitaria di Bologna Bologna Italy Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06794879 on ClinicalTrials.gov ↗ ← All trials in Italy