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临床试验/PER-041-00
PER-041-00已完成未知

Change from Haloperidol to Olanzapine in schizophrenic patients: an open study

ELI LILLY INTERAMERICA INC.,0 个研究点目标入组 0 人开始时间: 2000年7月18日最近更新:
适应症

试验速览

阶段
未知
状态
已完成

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Women or men, from 18 to 65 years of age in the visit 1.
  • Female patients with gestational potential should use a medically accepted means of contraception.
  • Each patient must have a sufficient level of understanding to communicate intelligently with the researcher, nurse and study coordinator.
  • Patients must be reliable. They must agree to cooperate with all the tests and exams required by the protocol.
  • Each patient (or authorized legal representative of the patient) must understand the nature of the study and sign an informed consent.
  • Patients must meet the criteria for schizophrenia defined in the DSMIV.
  • Patients must have been treated with haloperidol for a minimum of 6 weeks before entering the study.
  • Patients must have a total SAS score of> 3.

排除标准

  • Women who are pregnant or nursing.
  • Severe illnesses, including hepatic, renal, gastroenterological, respiratory, cardiovascular (including ischemic heart disease), endocrinological, neurological, immunological or hematological diseases, such as anticipating hospitalization within 3 months or death within 3 years.
  • Hyperthyroidism or hyperthyroidism uncorrected.
  • Acute angle glaucoma.
  • One or more attacks without a clear and determined etiology. Leukopenia or history of leukopenia without a clear and determined etiology.
  • History of severe allergies or adverse reactions to multiple medications.
  • Abuse or dependence of any substance (alcohol or other drugs) within the previous 3 months.
  • Judged clinically as seriously at risk of suicide.
  • Participation in a clinical trial of another research substance within 1 month (30 days) before entering the study (visit 1).
  • Any other medication concomitant with primary activity of the central nervous system, different from that specified in section 3.8.
  • Treatment with a neuroleptic injectable deposit prior to visit 1.
  • Previous exposure to olanzapine.
  • Treatment with lithium, anticonvulsants, benzodiazepines, antidepressants (except fluoxetine), psychostimulants, reversible monoamine oxidase monoamine oxidase inhibitors, reserpine, guanethidine or guanadrel, within week 1 before visit 2.
  • Any patient treated with clozapine within 4 weeks prior to visit 2.
  • Treatment with inhibitors of the non-reversible monoamine oxidase within 2 weeks prior to visit 2.
  • Fluoxetine treatment within 4 weeks prior to visit 2.
  • The use of anticholinergics as prophylaxis is prohibited.
  • More than 20 mg. of haloperidol the last 2 days before the visit 2.

研究者

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