drugset / Trial / NCT01889290

Methylnaltrexone Pharmacokinetics in Neurointensive Care Patients

NCT01889290

Phase 1 Completed 9 enrolled University of Zurich
NaSingle-groupOpen-labelTreatment

Summary

* Assessment of pharmacokinetic parameters of once daily subcutaneously administered methylnaltrexone in 10 evaluable neurointensive care patients. * Quantification of methylnaltrexone passage through the blood-brain-barrier in critically ill patients with severe cerebral affections. * Observation of laxation response after methylnaltrexone application and relation to plasma concentrations of methylnaltrexone. * Assessing the safety of once daily administered methylnaltrexone in neurointensive care patients. * Trial with medicinal product

Timeline

Start
2014-02
Primary completion
2016-06
Completion
2016-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Methylnaltrexone Other / unclassified 12 mg Subcutaneous

Indications