PREVACT : Preventive REversal of Vitamine K Antagonist in Minor Craniocerebral Trauma

Phase 3

Terminated

• Conditions: Craniocerebral Trauma; Coagulation; Intravascular; Haemorrhage
• Interventions: Drug: Reversion

• Registration Number: NCT01961804
• Lead Sponsor: University Hospital, Angers

Brief Summary

The occurence of a minor craniocerebral trauma in patients receiving vitamine K antagonist treatment leads to a high risk of bleeding.

Current guidelines recommend to perform a CT scan, and, in case of intracranial bleeding, to reverse anticoagulation with concomitant administration of prothrombin complex concentrates (PCCs) and vitamin K.

However, even if a reversion is performed, the prognostic of post-traumatic intracranial bleeding remain bad.

The investigators hypothesize that, for patients admitted in an emergency department after a minor head trauma and receiving anticoagulant treatment, a systematic preventive reversion with PCCs can lead to a significant reduction of intracranial haemorrhage and can also improve the neurological prognostic of patients versus the current strategy.

PREVACT will test this hypothesis, in an open label, randomized, multicentre, clinical trial involving 400 patients.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2013-10-09
• Study First Submitted QC: 2013-10-10
• Study First Posted: 2013-10-11
• Study Start: 2014-03
• Primary Completion: 2020-02-28
• Status Verified: 2020-08
• Study Completion: 2020-09-03
• Last Update Submitted: 2021-04-26
• Last Update Posted: 2021-04-27

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 202

Inclusion Criteria

• Admission in an emergency departement for a recent and isolated minor head trauma with at least one of the following characteristic : a period of alteration in the level of consciousness, a period of loss of consciousness (< 30 min), a posttraumatic amnesia, persistant posttraumatic headache, repeated vomitting (at least 2 episodes) or any other neurological sign such a convulsion or a localised neurological sign, wound of the scalp or the face testifying of the importance of the cranial trauma...
• Subject receiving anticoagulant treatment with anti-vitamin K for the treatment of atrial fibrillation (AF)
• Initial ED Glasgow Coma Scale (GCS) score of ≥13
• Achievable follow up
• Informed consent form signed by the patient or if he/she isn't able an emergency inclusion can be realised.

Exclusion Criteria

• Delay between the minor head trauma and the possible preventive PCC's administration > 6h
• Subject receiving anticoagulant treatment other than anti vitamin K (heparin, fondaparinux, dabigatran, rivaroxaban, apixaban...)
• Subject receiving anticoagulant treatment for other reason than a AF
• Subject on antiplatelet treatment (except the use of low dose of aspirin (≤ 100 mg/day)
• Delocalised biology INR in capillary blood < 1.5 if it's available (only in departement where this analyse is a usual practice)
• Haemorrhage or suspected haemorrhage other than intracranial which could led to a reversion of the anticoagulation
• Head trauma associated with one or further potential haemorrhagic traumatic lesions
• Subject who reject the use of products derived from human blood
• Women who are pregnant
• Subject with any condition that, as judged by the investigator, would place the subject at increased risk of harm if he/she participated in the study
• Subject without social security registered

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Actual recommendations	Reversion	Current guidelines recommend to perform a CT scan and realise the anticoagulation reversion only in case of intracranial bleeding diagnosed.
Preventive reversion	Reversion	Realise a preventive reversion before performing any CT scan.

Primary Outcome Measures

Name	Time	Method
Percentage of intracranial bleeding diagnosed in CT scan	24 hours +/- 4 hours	This primary outcome measure will be analyse in a centralised place by two neuro-radiologist in blind of the randomised group.

Secondary Outcome Measures

Name	Time	Method
Percentage of patient having a decrease in their autonomy	3 months	A loss of at least one point in the Glasgow Outcome Score Extended
Percentage of patient having a systemic or neurologic ischemic attacks	1 month
Volumetric measure of intracranial haemorrhage	CT scan performed 24 hours +/-4 after inclusion	This secondary outcome measure will be analyse in a centralised place by two neuro-radiologist in blind of the randomised group.

Trial Locations

Locations (21)

Ch Longjumeau; 🇫🇷 Longjumeau, France

CHU Angers; 🇫🇷 Angers, France

Chu Toulouse; 🇫🇷 Toulouse, France

Chu Nantes; 🇫🇷 Nantes, France

CHU METZ; 🇫🇷 Metz, France

Chg Montauban; 🇫🇷 Montauban, France

CH Agen; 🇫🇷 Agen, France

CHG du Mans; 🇫🇷 Le Mans, France

CHU Clermont Ferrand; 🇫🇷 Clermont Ferrand, France

CHU Chateauroux; 🇫🇷 Chateauroux, France

Ch Les Sables D'Olonne; 🇫🇷 Les Sables d'Olonne, France

Chu Tours; 🇫🇷 Tours, France

Chu Tenon; 🇫🇷 Paris, France

Ch Saint Malo; 🇫🇷 Saint Malo, France

CHU Nice; 🇫🇷 Nice, France

Ch Annecy; 🇫🇷 Annecy, France

HCL Edouard Herriot; 🇫🇷 Lyon, France

CHU Pitié Salpétrière; 🇫🇷 Paris, France

Chu Poitiers; 🇫🇷 Poitiers, France

Chu Saint Brieuc; 🇫🇷 Saint Brieuc, France

Ch Versailles; 🇫🇷 Versailles, France