CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 140 enrolled
Drug / intervention
French Lyophilized Plasma +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02736812
NCT02736812Phase 3Completed

Interest of Pre-hospital Administration of Lyophilized Plasma to Prevent or Treat Coagulopathy Associated With Post-traumatic Hemorrhagic Shock (PREHO-PLYO Study )

French Defence Health Service·interventional·Posted Apr 13, 2016·Updated Jan 7, 2020

In Brief

A Phase 3 clinical trial evaluating French Lyophilized Plasma and Normale Saline Solution for Shock Hemorrhagic. Completed, enrolled 140 participants across 22 sites.

Detailed Summary

In severe bleeding due to trauma, a decrease in coagulation factors maintains and promotes bleeding. The plasma allows, through its contribution of coagulation factors, early prevention or correction of this post-trauma induced coagulopathy. This study aims to measure the effectiveness of pre-hospital FLYP administration in case of traumatic hemorrhagic shock, in the occurrence or the treatment of a post traumatic induced coagulopathy. Study Design This is a randomized controlled multicenter open label study in two parallel groups. Eligibility criteria : adult, victim of a hemorrhagic shock of traumatic origin with \[systolic blood pressure \<70 mmHg\] or Shock Index \>1.1 The patients will receive either FLYP either the usual treatment as given in the recommendations for best practice. The primary endpoint is the International Normalized Ratio (INR) at hospital admission. The study must confirm the link between causality of early administration of plasma in improving post-traumatic coagulopathy. The study must show safe usage in out-of-hospital situations and the ability of medical staff to meet the requirements of the health authorities in terms of product use as well as in terms of traceability of the victims and the treatment they received.

Study Details

Timeline

Phase 3CompletedFinished
20162017201820192020202120222023202420252026
First PostedApr 13, 2016
Enrollment StartApr 1, 2016
Primary CompletionOct 31, 2019
Study CompletionNov 30, 2019
TodayJul 2, 2026
Enrollment to primary: 3.6 yearsPosted 10.2 years ago

Interventions

French Lyophilized Plasmabiological

During the pre-hospital phase, the main events related to this arm are * Blood samples taken before treatment (TP, fibrinogen, platelets, RBC, grouping) * Usual pre-hospital care according to recommendations in best practices * Administration of FLYP

Normale Saline Solutionbiological

During the pre-hospital phase, the main events related to this arm are * Blood samples taken before treatment (TP, fibrinogen, platelets, RBC, grouping) * Usual pre-hospital care according to recommendations in best practices * Administration of Normale Saline Solution