Actively Recruiting
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
Eligibility Criteria
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
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
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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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