NCT04282382

Brief Summary

The purpose of this study is to examine factors, impact and outcome on perioperative blood transfusion for pediatric patients.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
66

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Mar 2020

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 17, 2020

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 24, 2020

Completed
6 days until next milestone

Study Start

First participant enrolled

March 1, 2020

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2020

Completed
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

October 15, 2020

Completed
Last Updated

August 24, 2021

Status Verified

August 1, 2021

Enrollment Period

7 months

First QC Date

February 17, 2020

Last Update Submit

August 23, 2021

Conditions

Transfusion

Keywords

Transfusion, Pediatric, Patient Blood Management

Outcome Measures

Primary Outcomes (2)

  • Number of children being transfused intraoperative

    Amount of transfused pRBC, plasma, thrombocytes will be evaluated in children undergoing surgery

    01.04.2018 to 31.10.2019

  • Documented transfusion indication

    Physiologic transfusion triggers will be evaluated (Hb Level, lactate, venous O2 saturation, levels of catecholamines)

    01.04.2018 to 31.10.2019

Eligibility Criteria

Age0 Years - 17 Years
Sexall
Age GroupsChild (0-17)
Sampling MethodNon-Probability Sample
Study Population

All pediatric patients being operated an receiving transfusion will be included.

You may qualify if:

  • Operation
  • Anaesthesia
  • Transfusion (pRBC, plasma or platelets)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Anaesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt, Goethe University

Frankfurt, North Rhine-Westphalia, 60598, Germany

Location

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principle Investigator

Study Record Dates

First Submitted

February 17, 2020

First Posted

February 24, 2020

Study Start

March 1, 2020

Primary Completion

October 1, 2020

Study Completion

October 15, 2020

Last Updated

August 24, 2021

Record last verified: 2021-08

Locations

DE(1)