drugset / Trial / NCT03713658
A Study to Evaluate the Ability of Conducting a Study of Oral Risperidone Followed by Paliperidone Palmitate in Rwandan Healthcare Facilities
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |