Actively Recruiting

All Genders
ID06797921

Analysis of the Hospital Node in the Management of Acute Events in Pediatric Palliative Care Patients

Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2025-01-29

350

Participants Needed

7

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to understand how hospital care affects children under pediatric palliative care during urgent health events. Children in pediatric palliative care often face repeated hospital stays, which tend to be longer and sometimes exceed 100 days. Hospitalizations for cancer patients usually involve treatment and diagnostic procedures, while non-cancer patients are often admitted due to complications affecting various organs. The number of children needing this care is rising due to advances that have increased survival rates in severe illnesses. The study will observe hospital admissions and emergency room visits of pediatric patients eligible for palliative care, focusing on how these acute events are managed. No specific treatments are given, as this is an observational study examining existing hospital practices and patient experiences. The study will collect data over about one year to evaluate the role of hospital care in managing these urgent health situations. Participants will be children under 18 years who qualify for pediatric palliative care based on established criteria. Researchers will track hospital and emergency room admissions to understand patterns and outcomes. This includes gathering information about hospitalization frequency and duration. The study aims to provide insights that could improve coordination and care for children with complex medical needs, ensuring their treatment goals and family communication are well supported.

CONDITIONS

Brief Title

Analysis of the Hospital Node in the Management of Acute Events of Patients Referred to Pediatric Palliative Care

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Living patients younger than 18 years at the time of the event
  • Patients with conditions eligible for pediatric palliative care as defined by the Association for Children's Palliative Care and the Royal College of Pediatrics and Child Health
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

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

Duration - Approximately 1 year

Participants who are eligible for pediatric palliative care are observed to quantify emergency room and hospital admissions over time.

Visits occur as needed based on acute events and hospital admissions

Trial Site Locations

Total: 7 locations

1

IRCCS Azienda Ospedaliero - Universitaria di Bologna, U.O. Cardiologia Pediatrica

Bologna, Bologna, Italy, 40138

Not Yet Recruiting

2

IRCCS Azienda Ospedaliero - Universitaria di Bologna, U.O. Neonatologia e Terapia Intensiva Neonatale

Bologna, Bologna, Italy, 40138

Actively Recruiting

3

IRCCS Azienda Ospedaliero - Universitaria di Bologna, U.O. Oncoematologia Pediatrica

Bologna, Bologna, Italy, 40138

Actively Recruiting

4

IRCCS Azienda Ospedaliero - Universitaria di Bologna, U.O. Pediatria d'Urgenza, Pronto Soccorso e Osservazione Breve ed Intensiva

Bologna, Bologna, Italy, 40138

Actively Recruiting

5

IRCCS Azienda Ospedaliero - Universitaria di Bologna, U.O. Pediatria

Bologna, Bologna, Italy, 40138

Actively Recruiting

6

IRCCS Azienda Ospedaliero - Universitaria di Bologna, U.O. Rianimazione Pediatrica

Bologna, Bologna, Italy, 40138

Actively Recruiting

7

IRCCS Istituto delle Scienze Neurologiche di Bologna, U.O.C. Neuropsichiatria dell'età pediatria

Bologna, Bologna, Italy, 40138

Actively Recruiting

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Research Team

D

Daniele Zama, 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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