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Fibrinogen for Treatment of Pediatric Dilutional Coagulopathy. FibPaed Study.

University of Zurich (UZH) logo

University of Zurich (UZH)

Status and phase

Completed
Phase 4

Conditions

Hemorrhage
Blood Coagulation Disorders

Treatments

Drug: Human fibrinogen concentrate

Study type

Interventional

Funder types

Other

Identifiers

NCT01487837
KEK-ZH-Nr. 2011-0440

Details and patient eligibility

About

The purpose of this study is to compare two different thromboelastometry (ROTEM) trigger levels for administration of human fibrinogen concentrate (Haemocomplettan P) in the treatment of perioperative dilutional coagulopathy during major pediatric surgery. The study hypothesis is that administration of fibrinogen concentrate triggered by a ROTEM FibTEM MCF < 13 mm might reduce the total amount of transfused red cell concentrate during 24 hours after start of surgery as compared to a trigger level of ROTEM FibTEM MCF < 8 mm.

Enrollment

57 patients

Sex

All

Ages

6 months to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Males and Females
  • Age 6 months to 17 years
  • Scheduled for elective scoliosis surgery or major craniofacial surgery
  • Written informed consent has been obtained
  • Intraoperative hypofibrinogenemia according to definition of treatment groups

Exclusion criteria

  • Preexisting congenital or acquired coagulation disorder
  • Medical history of estimated increased bleeding tendency
  • Ongoing coagulation therapy
  • Clinical signs or diagnosis of acute thromboembolism
  • Intolerance of study drug
  • Participation at another clinical trial
  • Pregnant or lactating women

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

57 participants in 2 patient groups

Fibrinogen if FibTEM < 8 mm
Active Comparator group
Description:
Administration of fibrinogen concentrate if ROTEM FibTEM revealed MCF \< 8 mm
Treatment:
Drug: Human fibrinogen concentrate
Fibrinogen if FibTEM < 13 mm
Experimental group
Description:
Administration of fibrinogen concentrate if ROTEM FibTEM revealed MCF \< 13 mm
Treatment:
Drug: Human fibrinogen concentrate

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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