An observational study in Analgesia and Sensation, Hyperalgesic, sponsored by IRCCS Azienda Ospedaliero-Universitaria di Bologna. Recruiting at 1 site in Italy. Per ClinicalTrials.gov, last updated 2025-01-27.
Sponsored by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Observational
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.
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.
166 studies on the registry are indexed under Hyperalgesia; 14 are open to participants now.
This study's planned enrollment of 700 is above the median of 87 across 18 observational studies indexed under Hyperalgesia.
Browse Hyperalgesia studies →IRCCS Azienda Ospedaliero-Universitaria di Bologna is the lead sponsor of 511 studies on the registry; 287 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Parents of children between the ages of 2 months and 14 years who are afferent to the withdrawal clinic of the U.O. Urgent Pediatrician, Emergency Department and Short and Intensive Observation of IRCCS - Azienda Ospedaliero Universitaria di Bologna Policlinico di Sant'Orsola.
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Exclusion Criteria:
Identify the parent's degree of agreement/disagreement with pediatric procedural analgosedation practices and factors that may influence it
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
Time frame: through study completion, an average of 1 year
Started Dec 2024 (actual). Primary completion is estimated for Dec 2025, 12 months after the start.
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Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.
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