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Seroquel XR in the Long Term Treatment of Schizophrenia

Seroquel XR in the Long Term Treatment of Schizophrenia Focus on Affective Symptoms

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01202617
Acronym
SereNIS
Enrollment
1606
Registered
2010-09-16
Start date
2010-09-30
Completion date
2011-10-31
Last updated
2011-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relapse in Schizophrenia

Keywords

Seroquel XR, schizophrenia, relapse prevention

Brief summary

The purpose of the study is to determine whether the Seroquel XR treatment for 6 months improves the relapse prevention in schizophrenic outpatients

Interventions

None listed

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* schizophrenic outpatients on at least 600 mg Seroquel XR treatment for at least 1 month

Exclusion criteria

* Severe cerebro- and cardiovascular disease, severe hepatic impairment, gravidity

Design outcomes

Primary

MeasureTime frame
Rate of patients remained relapse free after 6 months of treatmenton the 60th day of treatment

Secondary

MeasureTime frame
connection between relapse and affective symptomson the 60th day of treatment

Countries

Hungary

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026