Observational study on long-term treatment of schizophrenia with atypical antipsychotics
An Observational Study on Atypical Antipsychotics Long-term Treatment Patients With Schizophrenia
This study is testing how well long-term treatment with certain antipsychotic medications works for people with schizophrenia in China.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 3000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Shanghai Mental Health Center Academic / other |
| Locations | 1 site (Shanghai, Shanghai Municipality) |
| Trial ID | NCT02640911 on ClinicalTrials.gov |
What this trial studies
This observational study aims to evaluate the safety and efficacy of long-term treatment with atypical antipsychotics in patients diagnosed with schizophrenia in China. The study will involve a cohort of 3000 patients and will assess various factors including symptoms, social functioning, recurrence rates, and hospitalization. Participants will undergo multiple assessments over a period of 156 weeks, including physical examinations, laboratory tests, and monitoring of adverse events. The study focuses on medications such as quetiapine, olanzapine, and clozapine, among others.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who have a diagnosis of schizophrenia and are currently taking or will take atypical antipsychotics.
Not a fit: Patients who are participating in other clinical studies or have conditions that make them unsuitable for this study may not benefit.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the long-term safety and effectiveness of atypical antipsychotics for patients with schizophrenia.
How similar studies have performed: Other studies have shown varying degrees of success in evaluating the safety and efficacy of atypical antipsychotics, making this study a continuation of existing research rather than a completely novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. An in-patient or out-patient (male or female) and aged ≥18 years 2. A diagnosis of schizophrenia,DSM-IV(Diagnostic and Statistical Manual Diploma in Social Medicine-IV) 3. Subjects must have the ability to effectively communicate with investigator,complete study related documents, comprehend the key components of the consent form and must provide written informed consent to participate in the study prior to any study specific assessments or procedures. 4. Patients are taking or will take atypical antipsychotics which include quetiapine, olanzapine, risperidone, aripiprazole, ziprasidone, paliperidone , amisulpride , perospirone and clozapine Exclusion Criteria: 1. Participation in other clinical studies. 2. Other conditions which, in the investigator's judgment, render patients unsuitable for the clinical study.
Where this trial is running
Shanghai, Shanghai Municipality
- Shanghai Mental Health Center — Shanghai, Shanghai Municipality, China (Recruiting)
Study contacts
- Study coordinator: Huafang Li, PH.D
- Email: lhlh_5@163.com
- Phone: 86-21-34773128
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.