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NA - NA

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2016-004247-37-FR
Enrollment
350
Registered
2017-05-04
Start date
2017-05-04
Completion date
Unknown
Last updated
2021-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

coagulopathy secondary to traumatic hemorrhagic shock

Interventions

Trade Name: KANOKAD 25 UI/ml de facteur IX, poudre et solvant pour solution injectable Product Name: kanokad Pharmaceutical Form: Powder and solution for solution for injection Pharmaceutical form of

Sponsors

University Hospital Grenoble
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: NA Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 350 F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: NA

Design outcomes

Primary

MeasureTime frame
Main Objective: NA;Secondary Objective: NA;Primary end point(s): NA;Timepoint(s) of evaluation of this end point: NA

Secondary

MeasureTime frame
Secondary end point(s): NA;Timepoint(s) of evaluation of this end point: NA

Countries

France

Contacts

Public Contactprincipal investigator

University Hospital Grenoble

pbouzat@chu-grenoble.fr

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026