Is Initial Response to Low Dose Risperidone Predictive for Outcome in

Status Terminated

Clinical Trial Summary

Clinical Trial Description

Risperidone at low dosage is often used as treatment of acute anxiety symptom. However, patients may be either responder or not. Here we hypothesized that the early response to a low dose of risperidone is predictive to risperidone efficiency. Subjects with acute anxiety symptoms (Hospital anxiety depression scale) and risperidone prescription would be proposed to be enrolled in the study. After acceptation, the fulfil questionnaires (MINI, PCL-s-V) then they interacts with test on computers (PVT, 2nBack, Iowa gambling task) and give saliva and receive an actimetric watch (D0). They begin the treatment on the evening (0.5mg risperidone/day). The following day, they come back to hospital and they fulfil the same tests, questionnaires and samples (D1). 12 week after, they come again to hospital to fulfil the same tests, questionnaires and samples (W12). Between D1 and S12, the psychiatrist may change the treatment, adding other treatment or modifying risperidone treatment (increasing dosage up to 2mg/day or removing it). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03227562
Study type	Interventional
Source	Institut de Recherche Biomedicale des Armees
Contact
Status	Terminated
Phase	Phase 3
Start date	September 1, 2017
Completion date	December 1, 2021

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Is Initial Response to Low Dose Risperidone Predictive for Outcome in Anxiety?

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms