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NCT03782025: VITAKOAG

Effect of Vitamin K in Critically Ill Patients

Completed Last updated 18 March 2021
What this trial tests

trial testing Phytomenadione in Coagulation Factor Deficiency in 52 participants. Completed in 20 March 2020.

Timeline
13 February 2019
Primary endpoint
20 March 2020
20 March 2020

Quick facts

Lead sponsorRegion Skane
StatusCompleted
Study typeOBSERVATIONAL
Enrollment52
Start date13 February 2019
Primary completion20 March 2020
Estimated completion20 March 2020
Sites2 locations across Sweden

Drugs / interventions tested

Conditions studied

Sponsor

Region Skane — full company profile →

Who can join

18 and older, any sex, with Coagulation Factor Deficiency or Coagulopathy, Consumption. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Critically ill patients with spontaneously prolonged pro-thrombin time, where administration of intravenous administration of phytomenadione (vitamin K) has been ordered by the treating physician will be identified. After signed informed consent baseline samples will be collected. Phytomenadione will be given and 24 hours after administration new blood samples will be collected. Several different advanced coagulation and vitamin K-assays will be performed before and 24 hours after vitamin K administration.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Coagulation Factor Deficiency

Currently open trials in the same condition.

Other Region Skane trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03782025.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing