drugset / Trial / NCT03001193

Effect of Tafoxiparin to Treat Primary Slow Progress of Labor Including Prolonged Latent Phase and Labor Arrest

NCT03001193

Phase 2 Completed 361 enrolled Dilafor AB
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study will be designed as a double-blind, placebo-controlled, parallel-group, dose-finding study with one group treated with placebo and three groups treated with tafoxiparin in three different infusion concentration levels, respectively. The intravenous infusion will be initiated by a pre-defined bolus dose infusion.

Timeline

Start
2016-12
Primary completion
2018-11
Completion
2019-05

Drugs

EvaluationDrugModalityDoseRoute
Subject DF01 Other / unclassified 5 mg Intravenous
Subject DF01 Other / unclassified 15 mg Intravenous
Subject DF01 Other / unclassified 25 mg Intravenous
Background Oxytocin Peptide

Indications