Transfusion-requirements in Septic Shock Trial

PHASE3CompletedINTERVENTIONAL
Enrollment

1,005

Participants

Timeline

Start Date

November 30, 2011

Primary Completion Date

March 31, 2014

Study Completion Date

April 30, 2014

Conditions
Septic Shock
Interventions
BIOLOGICAL

SAGM (Saline-Adenine-Glucose-Mannitol) blood transfusion

One unit prestorage, leuko-depleted SAGM blood at haemoglobin at 9.0 g/dl (5.6 mM) or less at point-of-care testing

BIOLOGICAL

SAGM (Saline-Adenine-Glucose-Mannitol) blood transfusion

One unit prestorage, leuko-depleted SAGM blood at haemoglobin 7.0 g/dl (4.3 mM) or less at point-of-care testing

Trial Locations (32)

Unknown

Ålborg University Hospital, Aalborg

Aarhus University Hospital, NBG, Aarhus

Aarhus University Hospital, Skejby, Aarhus

Bispebjerg Hospital, Copenhagen

Glostrup Hospital, Copenhagen

Hvidovre Hospital, Copenhagen

Rigshospitalet, Copenhagen

Gentofte Hospital, Gentofte Municipality

Herning Hospital, Herning

Hjørring Hospital, Hjørring

Holbæk Hospital, Holbæk

Horsens Hospital, Horsens

Kolding Hospital, Kolding

Køge Hospital, Køge

Næstved Hospital, Næstved

Randers Hospital, Randers

Slagelse Hospital, Slagelse

Sønderborg Hospital, Sønderborg

Vejle Hospital, Vejle

Helsinki University Hospital, Helsinki

Joensuu Hospital, Joensuu

Tampere University Hospital, Tampere

Ålesund Hospital, Ålesund

Haukeland University Hospital, Bergen

Akershus University Hospital, Oslo

Stavanger University Hospital, Stavanger

Halmstad Hospital, Halmstad

Helsingborg Hospital, Helsingborg

Karolinska Hospital, Huddinge, Stockholm

Karolinska Institutet Solna, Stockholm

Södersjukhuset, Stockholm

Växjö Hospital, Vaxjo

All Listed Sponsors
collaborator

Copenhagen Trial Unit, Center for Clinical Intervention Research

OTHER

collaborator

Rigshospitalet, Denmark

OTHER

collaborator

University of Copenhagen

OTHER

lead

Scandinavian Critical Care Trials Group

OTHER

NCT01485315 - Transfusion-requirements in Septic Shock Trial | Biotech Hunter | Biotech Hunter