Submission date
08/09/2005
Registration date
06/10/2005
Last edited
03/03/2009
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Injury, Occupational Diseases, Poisoning
Retrospectively registered
? Protocol not yet added
? SAP not yet added
Results added
? Raw data not yet added
Study completed

Plain English Summary

Not provided at time of registration

Study website

Contact information

Type

Scientific

Contact name

Prof Arun Gupta

ORCID ID

Contact details

Department of Anaesthesia
Box 93
Cambridge
CB2 2QQ
United Kingdom
akg01@globalnet.co.uk

Additional identifiers

EudraCT/CTIS number

IRAS number

ClinicalTrials.gov number

Protocol/serial number

LREC 02/191

Study information

Scientific title

The effect of transfusion on cerebral oxygenation in traumatic brain injury: a randomised controlled trial

Acronym

Study hypothesis

Blood transfusion does not affect brain oxygenation in traumatic brain injury.

Ethics approval(s)

Not provided at time of registration

Study design

Randomised controlled trial

Primary study design

Interventional

Secondary study design

Randomised controlled trial

Study setting(s)

Hospital

Study type

Treatment

Patient information sheet

Condition

Traumatic brain injury

Intervention

Blood transfusion - the patients are randomised to 3 different transfusion triggers

Intervention type

Other

Primary outcome measure

Brain tissue oxygen partial pressure.

Secondary outcome measures

1. Jugular venous saturation
2. Lactate/pyruvate ratio
3. Neurological outcome
4. Cerebral haemodynamics

Overall study start date

01/07/2002

Overall study end date

01/12/2005

Reason abandoned (if study stopped)

Eligibility

Participant inclusion criteria

1. Greater than 16 years of age
2. Severe traumatic brain injury (i.e. traumatic brain injury resulting in a resuscitated Glasgow coma score of less than or equal to 8, resulting in intracranial hypertension (greater than 20 mmHg for greater than 10 minutes), or requiring neurosurgical intervention
3. Informed assent from the next of kin

Participant type(s)

Patient

Age group

Adult

Sex

Both

Target number of participants

30

Participant exclusion criteria

1. Active haemorrhage
2. Active coronary ischaemia as judged by dynamic electrocardiogram (ECG) changes or positive troponin levels not due to myocardial contusion
3. Inability to place cerebral oxygenation monitors
4. Failure to fall below allocated transfusion threshold during intracranial pressure (ICP) monitoring

Recruitment start date

01/07/2002

Recruitment end date

01/12/2005

Locations

Countries of recruitment

England, United Kingdom

Study participating centre

Department of Anaesthesia
Cambridge
CB2 2QQ
United Kingdom

Sponsor information

Organisation

Cambridge University Hospitals NHS Foundation Trust (UK)

Sponsor details

Addenbrooke's Hospital
Hills Road
Cambridge
CB2 2QQ
England
United Kingdom
jn254@cam.ac.uk

Sponsor type

Hospital/treatment centre

Website

http://www.cuh.org.uk/

ROR

https://ror.org/04v54gj93

Funders

Funder type

Research organisation

Funder name

Association of Anaesthetists of Great Britain and Ireland (UK)

Alternative name(s)

Funding Body Type

Funding Body Subtype

Location

Funder name

Intensive Care Society (UK)

Alternative name(s)

ICS

Funding Body Type

private sector organisation

Funding Body Subtype

Associations and societies (private and public)

Location

United Kingdom

Funder name

Codman (Johnson & Johnson) (UK)

Alternative name(s)

Funding Body Type

Funding Body Subtype

Location

Results and Publications

Publication and dissemination plan

Not provided at time of registration

Intention to publish date

Individual participant data (IPD) sharing plan

IPD sharing plan summary

Not provided at time of registration

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Results article results 01/03/2009 Yes No

Additional files

Editorial Notes