Actively Recruiting

Age: 27Days - 17Years
All Genders
NCT07070258

Pediatric Intensive Care Transport Registry

Led by Philipps University Marburg · Updated on 2025-07-20

1000

Participants Needed

2

Research Sites

266 weeks

Total Duration

On this page

Sponsors

P

Philipps University Marburg

Lead Sponsor

D

Deutsche Interdisziplinäre Vereinigung für Intensiv- und Notfallmedizin

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim is to establish a nationwide registry for pediatric intensive care transports in Germany. The project aims to describe and analyse the need for, and current practice of, specialised transports. These data could then be used for future demand planning.

CONDITIONS

Official Title

Pediatric Intensive Care Transport Registry

Who Can Participate

Age: 27Days - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Critically ill children aged at least 27 days with a corrected gestational age over 41 weeks
  • Maximum age of 17 years
  • Transport is interhospital
  • Transport is a critical care transport by a dedicated critical care team using an intensive care ambulance (Type C vehicle) or an air ambulance
  • Alternatively, transport is accompanied by a specialist in intensive care or emergency medicine
  • The transport destination is a critical care area such as an intensive care unit, trauma room, resuscitation area, operating theatre, emergency imaging, or emergency intervention
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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Trial Site Locations

Total: 2 locations

1

University of Dresden

Dresden, Germany, 01307

Actively Recruiting

2

Philipps University of Marburg

Marburg, Germany, 35043

Actively Recruiting

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Research Team

N

Nadine Mand, Dr. med.

CONTACT

S

Stefan Winkler, Dr. med.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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