drugset / Trial / NCT03713658

A Study to Evaluate the Ability of Conducting a Study of Oral Risperidone Followed by Paliperidone Palmitate in Rwandan Healthcare Facilities

NCT03713658

Phase 4 Completed 34 enrolled Janssen Research & Development, LLC
Non-randomizedSequentialOpen-labelHealth-services research

Summary

The purpose of this study is to evaluate the feasibility of conducting a study of oral risperidone followed by paliperidone palmitate for once monthly (PP1M) and paliperidone palmitate for every 3 months (PP3M) in rwandan healthcare facilities with mental healthcare capabilities.

Timeline

Start
2018-10-18
Primary completion
2019-12-02
Completion
2019-12-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Risperidone Other / unclassified 3 mg Oral
Subject paliperidone palmitate Unknown 50 mg Intramuscular
Subject paliperidone palmitate Unknown 75 mg Intramuscular
Subject paliperidone palmitate Unknown 100 mg Intramuscular
Subject paliperidone palmitate Unknown 150 mg Intramuscular
Subject paliperidone palmitate Unknown 175 mg Intramuscular
Subject paliperidone palmitate Unknown 263 mg Intramuscular
Subject paliperidone palmitate Unknown 350 mg Intramuscular
Subject paliperidone palmitate Unknown 525 mg Intramuscular

Indications