Actively Recruiting

All Genders
Healthy Volunteers
ID06794879

Survey of Parental Perception of Procedural Analgosedation in Children and Adolescents

Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2025-01-27

700

Participants Needed

1

Research Sites

55 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to understand parents' knowledge and feelings about procedural sedation used in children. It seeks to uncover any gaps in understanding and identify parents' expectations and concerns regarding sedation during medical procedures. The goal is to help improve communication between healthcare providers and parents and guide the development of training programs for healthcare personnel to better manage sedation and interactions with families. Parents or guardians of children aged 2 months to 14 years are asked to complete a survey about their perceptions of procedural sedation. No experimental treatments or changes to standard care are involved; all medical procedures will follow usual clinical practice in an outpatient setting. During the study, researchers will measure how much parents agree or disagree with current sedation practices and explore factors influencing their views. The survey results will be collected over about one year. This study involves only completing the survey alongside routine care, with no additional interventions or procedures for the child or parent.

CONDITIONS

Official Title

Survey for Parental Perception of Procedural Analgosedation in Pediatric Age.

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be a parent or guardian of a child between 2 months and 14 years old
  • The child is attending the withdrawal clinic
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

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Trial Site Locations

Total: 1 location

1

IRCCS Azienda Ospedaliero - Universitaria di Bologna

Bologna, Italy, Italy, 40138

Actively Recruiting

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Research Team

L

Laura Andreozzi, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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