Status:

COMPLETED

A Survey to Collect Treatment Experience Feedback From Patients, Physicians, Nurses and Carers After Switching to Paliperidone Palmitate 3-monthly

Lead Sponsor:

Janssen-Cilag International NV

Conditions:

Schizophrenia

Eligibility:

All Genders

18+ years

Brief Summary

The purpose of this study is to explore the experience with paliperidone palmitate 3-month formulation (PP3M) treatment of participants and their corresponding physicians, nurses and carers, to unders...

Eligibility Criteria

Inclusion

  • Have a diagnosis of schizophrenia (according to International Classification of Diseases \[ICD\]-10)
  • Be currently receiving PP3M and have previously received 4 to 6 injections of PP3M
  • Have the required language skills to participate in the online questionnaire, in the opinion of the physician
  • Be able and willing to provide their informed consent for study participation

Exclusion

  • Has received involuntary treatment with PP3M
  • Was switched to PP3M treatment within a clinical trial

Key Trial Info

Start Date :

November 21 2018

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

July 12 2019

Estimated Enrollment :

225 Patients enrolled

Trial Details

Trial ID

NCT03809325

Start Date

November 21 2018

End Date

July 12 2019

Last Update

April 27 2025

Active Locations (41)

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Page 1 of 11 (41 locations)

1

Chu Brugmann

Brussels, Belgium, 1020

2

Centre Médico Psychologique De Courbevoie

Asnières-sur-Seine, France, 92600

3

Centre Medico Psychologique

Cagnes-sur-Mer, France, 6800

4

Cabinet medical

Dax, France, 40100

A Survey to Collect Treatment Experience Feedback From Patients, Physicians, Nurses and Carers After Switching to Paliperidone Palmitate 3-monthly | DecenTrialz