Survey for Parental Perception of Procedural Analgosedation in Pediatric Age.

NCT ID: NCT06794879

Last Updated: 2025-01-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

700 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-12-11

Study Completion Date

2025-12-31

Brief Summary

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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.

Detailed Description

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The study involves the completion of a survey by Parents/Guardians, the remaining interventions will be performed following the normal care procedure outpatient regimen, according to normal clinical practice.

Conditions

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Analgesia Sensation, Hyperalgesic

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Parents of children between the ages of 2 months and 14 years who are afferent to the withdrawal clinic

Exclusion Criteria

* None
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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IRCCS Azienda Ospedaliero-Universitaria di Bologna

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Laura Andreozzi, MD

Role: PRINCIPAL_INVESTIGATOR

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Locations

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IRCCS Azienda Ospedaliero - Universitaria di Bologna

Bologna, Italy, Italy

Site Status RECRUITING

Countries

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Italy

Central Contacts

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Laura Andreozzi, MD

Role: CONTACT

0512143012

Facility Contacts

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Laura Andreozzi, MD

Role: primary

0512143012

Other Identifiers

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ProSed-24

Identifier Type: -

Identifier Source: org_study_id

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