CClinicalTrials.gg
CompletedNCT02350101Updated Jan 29, 2015

Massive Transfusion Protocol With Coagulation Algorithm

An observational study in Bleeding, sponsored by University of Zurich. Completed. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2015-01-29.

Sponsored by University of Zurich · Observational

Study type
Observational
Time perspective
Retrospective
Enrollment
243
Ages
18 Years and older
Sex
All
01

Study summary

In 2008 at the University Hospital Zurich (USZ) a massive transfusion protocol was introduced. Based on laboratory diagnostics and point of care (POC) devices including ROTEM.

Goal of this retrospective study is to evaluate the influence of this algorithm on coagulation, use of blood products, coagulation factors and ROTEM evolution.

Read the detailed description

In 2008 at the USZ a massive transfusion protocol was introduced. Based on laboratory diagnostics and POC (point of care) devices including ROTEM.

Goal of this retrospective study is to evaluate the influence of this algorithm on coagulation, use of blood products, coagulation factors and ROTEM evolution over three years (2008-2010)

02

Conditions studied

  • Bleeding
03

In context

Lead sponsor

University of Zurich is the lead sponsor of 1,030 studies on the registry; 130 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All patients needing massive transfusion (more than 10 RBCs)

Inclusion criteria

  • Massive transfusion

Exclusion criteria

Exclusion Criteria:

  • non
05

Study design

Time perspective
Retrospective
Enrollment
243 participants (actual)
Patient registry
No

Interventions

  • DeviceRotational thromboelastometry

    In bleeding patients point of care measurements are performed, in this case Rotational Thromboelastometry (ROTEM) to guide the use of blood products and coagulation factors.

06

What researchers measure

Primary outcomes

  1. Coagulation in ROTEM

    Point of care devices are used in bleeding patients. In the university hospital of Zurich an algorithm in the case of massive bleeding was introduced in 2008. The primary outcome measure is to investigate the changes of ROTEM parameters in the sense of amelioration reflected by better coagulation by using goal directed transfusions.

    Time frame: 3 years

Secondary outcomes

  1. Transfusion needs

    To evaluate the blood products and coagulation factors needed and to evaluate if there is a reduction between the time before the introduction of the algorithm compared to afterwards.

    Time frame: 3 years

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 29, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02350101
Lead sponsor
University of Zurich
Responsible party
Oliver Theusinger (PD Dr med, University of Zurich) — Principal investigator
First posted
Jan 29, 2015
Start date
Jan 2010
Primary completion
Dec 2012
Completion
Dec 2012
Last update
Jan 29, 2015

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2015. You cannot join it, but the record below documents what was studied.

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