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NCT04982055

Intravenous Versus Subcutaneous Administration of Low Molecular Weight Heparin for Thromboprophylaxis in Critically Ill Patients

Completed Phase 4 Last updated 29 July 2021
What this trial tests

Phase 4 trial testing Nadroparin (intravenous Infusion) in Critical Illness in 60 participants. Completed in 31 December 2020.

Timeline
8 April 2015
Primary endpoint
31 December 2020
31 December 2020

Quick facts

Lead sponsorClinique Saint Pierre Ottignies
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment60
Start date8 April 2015
Primary completion31 December 2020
Estimated completion31 December 2020

Drugs / interventions tested

Conditions studied

Sponsor

Clinique Saint Pierre Ottignies — full company profile →

Who can join

18 and older, any sex, with Critical Illness. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Objective: To compare the pharmacokinetic profiles of intravenous versus subcutaneous route of administration of LMWH for thromboprophylaxis in critically ill patients

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Pharmacokinetic profiles of intravenous versus subcutaneous administration of low molecular weight heparin for thromboprophylaxis in critically ill patients: A randomized controlled trial.
    De Schryver N, Serck N, Eeckhoudt S, Laterre PF, et al · · 2022 · cited 3× · PMID 35381407 · DOI 10.1016/j.jcrc.2022.154029

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Other recruiting trials for Critical Illness

Currently open trials in the same condition.

Other Clinique Saint Pierre Ottignies trials

Trials by the same sponsor.

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