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Effects of Transfusion Thresholds on Neurocognitive Outcome of Extremely Low Birth Weight Infants (ETTNO)

Primary Purpose

Anemia of Prematurity

Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
red blood cell transfusion
red blood cell transfusion
Sponsored by
University Hospital Tuebingen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anemia of Prematurity focused on measuring prematurity, anemia, transfusion

Eligibility Criteria

0 Days - 3 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infants with a birth weight of 400 - 999g

Exclusion Criteria:

  • Missing written parental consent.
  • Gestational age > 29 + 6/7 weeks
  • Major congenital anomalies (including chromosomal aberrations, cyanotic congenital heart defects, syndromes likely affecting long-term outcome, and major congenital malformations requiring surgical correction during newborn period).
  • Infants who died before 48 hours, infants in whom the clinical decision to withhold intensive care was made, infants who were not considered viable
  • Participation in another study with ongoing use of an unlicensed investigational product from 28 days before study enrollment until the end of the study

Sites / Locations

  • Neonatalklinikken
  • University Hospital of Aachen
  • Children's Hospital
  • Vivantes Children's Hospital
  • Charité University Children's Hospital
  • University Children's Hospital
  • Children's Hospital
  • University Children's Hospital
  • Children's Hospital
  • University Children's Hospital
  • University of Duesseldorf
  • Helios Children's Hospital
  • Children's Hospital
  • University Children's Hospital
  • University Children's Hospital
  • University Children's Hospital
  • University of Greifswald
  • Children's Hospital Eppendorf
  • Children's Hospital Altona
  • Children's Hospital
  • University Hospital of Leipzig
  • University of Luebeck
  • University Children's Hospital
  • University Hospital of Marburg
  • University Children's Hospital
  • University Children's Hospital
  • Children's Hospital
  • Children's Hospital St. Hedwig
  • DRK Kinderklinik
  • Children's Hospital
  • University Hospital of Tuebingen
  • University Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

"liberal" transfusion triggers

"restrictive" transfusion triggers

Arm Description

"liberal" guidelines for red blood cell transfusions

"restrictive" guidelines for red blood cell transfusions

Outcomes

Primary Outcome Measures

Incidence of death or major neurodevelopmental impairment
The primary outcome measure of this study will be the incidence of death or major neurodevelopmental impairment determined at 24 months of age corrected for prematurity (where major neurodevelopmental impairment is defined as any of the following: cognitive delay defined as mental developmental index (MDI) score of the Bayley Scales of Infant Development (2nd edition) < 85, cerebral palsy, or severe visual or hearing impairment

Secondary Outcome Measures

Full Information

First Posted
July 12, 2011
Last Updated
September 9, 2021
Sponsor
University Hospital Tuebingen
Collaborators
German Research Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT01393496
Brief Title
Effects of Transfusion Thresholds on Neurocognitive Outcome of Extremely Low Birth Weight Infants
Acronym
ETTNO
Official Title
Effects of Transfusion Thresholds on Neurocognitive Outcome of Extremely Low Birth Weight Infants (ETTNO)- a Blinded Randomized Controlled Multicenter Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Completed
Study Start Date
July 2011 (undefined)
Primary Completion Date
April 30, 2017 (Actual)
Study Completion Date
October 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Tuebingen
Collaborators
German Research Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To compare the effect of restrictive versus liberal red blood cell transfusion thresholds on long-term neurodevelopmental outcome in extremely low birth weight infants.
Detailed Description
Extremely low birth weight (ELBW) infants uniformly develop anemia of prematurity and frequently require multiple red blood cell transfusions (RBCT) during neonatal intensive care. The criteria currently applied to indicate RBCT in this population are based on expert opinion rather than evidence and conclusive data of long-term effects of RBCT practices do not exist. Both, giving RBCT to improve oxygen carrying capacity and restricting RBCT to avoid RBCT associated risks and costs potentially impair long-term development. The proposed blinded randomized controlled trial was designed and will be powered to compare the effect of restrictive versus liberal red blood cell transfusion guidelines on long-term neurodevelopmental outcome in ELBW infants. ELBW infants will be randomized to receive RBCT according to liberal or restrictive RBCT guidelines, which both reflect current practice in Germany and aim for a clinically relevant difference in mean hemoglobin concentrations. The primary outcome measure is the incidence of death or major neurodevelopmental impairment determined at 24 months of age corrected for prematurity. Key secondary outcomes are the incidences of individual components of the composite primary outcome, the mental and physical developmental index scores of the Bayley Scales of Infant Development (II edition), and growth. Safety analyses will assess the incidences of all major diseases of prematurity. The results of this trial may help to improve the quality of life of these patients and reduce long-term health care costs.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anemia of Prematurity
Keywords
prematurity, anemia, transfusion

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
1013 (Actual)

8. Arms, Groups, and Interventions

Arm Title
"liberal" transfusion triggers
Arm Type
Experimental
Arm Description
"liberal" guidelines for red blood cell transfusions
Arm Title
"restrictive" transfusion triggers
Arm Type
Active Comparator
Arm Description
"restrictive" guidelines for red blood cell transfusions
Intervention Type
Other
Intervention Name(s)
red blood cell transfusion
Intervention Description
Implementation of "liberal" guidelines for red blood cell transfusions in extremely low birth weight infants
Intervention Type
Other
Intervention Name(s)
red blood cell transfusion
Intervention Description
Implementation of "restrictive" guidelines for red blood cell transfusions in extremely low birth weight infants
Primary Outcome Measure Information:
Title
Incidence of death or major neurodevelopmental impairment
Description
The primary outcome measure of this study will be the incidence of death or major neurodevelopmental impairment determined at 24 months of age corrected for prematurity (where major neurodevelopmental impairment is defined as any of the following: cognitive delay defined as mental developmental index (MDI) score of the Bayley Scales of Infant Development (2nd edition) < 85, cerebral palsy, or severe visual or hearing impairment
Time Frame
24 months of age corrected for prematurity

10. Eligibility

Sex
All
Minimum Age & Unit of Time
0 Days
Maximum Age & Unit of Time
3 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infants with a birth weight of 400 - 999g Exclusion Criteria: Missing written parental consent. Gestational age > 29 + 6/7 weeks Major congenital anomalies (including chromosomal aberrations, cyanotic congenital heart defects, syndromes likely affecting long-term outcome, and major congenital malformations requiring surgical correction during newborn period). Infants who died before 48 hours, infants in whom the clinical decision to withhold intensive care was made, infants who were not considered viable Participation in another study with ongoing use of an unlicensed investigational product from 28 days before study enrollment until the end of the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Axel R Franz, MD
Organizational Affiliation
University Hospital of Tuebingen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Neonatalklinikken
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark
Facility Name
University Hospital of Aachen
City
Aachen
ZIP/Postal Code
52074
Country
Germany
Facility Name
Children's Hospital
City
Augsburg
ZIP/Postal Code
86156
Country
Germany
Facility Name
Vivantes Children's Hospital
City
Berlin
ZIP/Postal Code
12351
Country
Germany
Facility Name
Charité University Children's Hospital
City
Berlin
ZIP/Postal Code
13353
Country
Germany
Facility Name
University Children's Hospital
City
Bochum
ZIP/Postal Code
44791
Country
Germany
Facility Name
Children's Hospital
City
Cologne
ZIP/Postal Code
50375
Country
Germany
Facility Name
University Children's Hospital
City
Cologne
ZIP/Postal Code
50924
Country
Germany
Facility Name
Children's Hospital
City
Datteln
ZIP/Postal Code
45711
Country
Germany
Facility Name
University Children's Hospital
City
Dresden
ZIP/Postal Code
01307
Country
Germany
Facility Name
University of Duesseldorf
City
Duesseldorf
ZIP/Postal Code
40225
Country
Germany
Facility Name
Helios Children's Hospital
City
Erfurt
ZIP/Postal Code
99089
Country
Germany
Facility Name
Children's Hospital
City
Erlangen
ZIP/Postal Code
91054
Country
Germany
Facility Name
University Children's Hospital
City
Essen
ZIP/Postal Code
45122
Country
Germany
Facility Name
University Children's Hospital
City
Frankfurt
ZIP/Postal Code
60590
Country
Germany
Facility Name
University Children's Hospital
City
Giessen
ZIP/Postal Code
35385
Country
Germany
Facility Name
University of Greifswald
City
Greifswald
ZIP/Postal Code
17475
Country
Germany
Facility Name
Children's Hospital Eppendorf
City
Hamburg
ZIP/Postal Code
20246
Country
Germany
Facility Name
Children's Hospital Altona
City
Hamburg
ZIP/Postal Code
22763
Country
Germany
Facility Name
Children's Hospital
City
Hannover
ZIP/Postal Code
30625
Country
Germany
Facility Name
University Hospital of Leipzig
City
Leipzig
ZIP/Postal Code
04103
Country
Germany
Facility Name
University of Luebeck
City
Luebeck
ZIP/Postal Code
23538
Country
Germany
Facility Name
University Children's Hospital
City
Magdeburg
ZIP/Postal Code
39120
Country
Germany
Facility Name
University Hospital of Marburg
City
Marburg
ZIP/Postal Code
35033
Country
Germany
Facility Name
University Children's Hospital
City
Muenster
ZIP/Postal Code
48149
Country
Germany
Facility Name
University Children's Hospital
City
Munich
ZIP/Postal Code
80337
Country
Germany
Facility Name
Children's Hospital
City
Nuremberg
ZIP/Postal Code
90471
Country
Germany
Facility Name
Children's Hospital St. Hedwig
City
Regensburg
ZIP/Postal Code
93049
Country
Germany
Facility Name
DRK Kinderklinik
City
Siegen
ZIP/Postal Code
57072
Country
Germany
Facility Name
Children's Hospital
City
Stuttgart
ZIP/Postal Code
70176
Country
Germany
Facility Name
University Hospital of Tuebingen
City
Tuebingen
ZIP/Postal Code
72076
Country
Germany
Facility Name
University Children's Hospital
City
Ulm
ZIP/Postal Code
89075
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
22298226
Citation
ETTNO Investigators. The 'Effects of Transfusion Thresholds on Neurocognitive Outcome of Extremely Low Birth-Weight Infants (ETTNO)' Study: Background, Aims, and Study Protocol. Neonatology. 2012 Jun;101(4):301-305. doi: 10.1159/000335030. Epub 2012 Jan 27.
Results Reference
background
PubMed Identifier
32780138
Citation
Franz AR, Engel C, Bassler D, Rudiger M, Thome UH, Maier RF, Krageloh-Mann I, Kron M, Essers J, Buhrer C, Rellensmann G, Rossi R, Bittrich HJ, Roll C, Hohn T, Ehrhardt H, Avenarius S, Korner HT, Stein A, Buxmann H, Vochem M, Poets CF; ETTNO Investigators. Effects of Liberal vs Restrictive Transfusion Thresholds on Survival and Neurocognitive Outcomes in Extremely Low-Birth-Weight Infants: The ETTNO Randomized Clinical Trial. JAMA. 2020 Aug 11;324(6):560-570. doi: 10.1001/jama.2020.10690. Erratum In: JAMA. 2022 Jul 12;328(2):217.
Results Reference
result
PubMed Identifier
34932836
Citation
Carson JL, Stanworth SJ, Dennis JA, Trivella M, Roubinian N, Fergusson DA, Triulzi D, Doree C, Hebert PC. Transfusion thresholds for guiding red blood cell transfusion. Cochrane Database Syst Rev. 2021 Dec 21;12(12):CD002042. doi: 10.1002/14651858.CD002042.pub5.
Results Reference
derived

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Effects of Transfusion Thresholds on Neurocognitive Outcome of Extremely Low Birth Weight Infants

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