MedPath

Reboxetine Adjuvant Therapy for the Treatment of Schizophrenia

Phase 1
Conditions
Schizophrenia
Registration Number
NCT00409201
Lead Sponsor
Abarbanel Mental Health Center
Brief Summary

30 patients will randomly be selected and will be administered either reboxetine or a placebo. changes in cognition and behavior will be assessed by computer tests and scales during a six week study period.

Detailed Description

all participants will be administered panss, sans, esrs, calgary, progesterom, sexual functioning scale, ham-a, covy, hamilton depression scale, and cgi and cgi improved rating on the first visit, as well as blood tests, ecg and weight. they will then be tested using a computer cognitive test (cogscan test) that lasts about 45 minutes. next, they will be given either a two week dose of placebo or treatment (2 mg \* 2 daily for first week, then 4 mg. day, 2 mg. night for the second week). after two weeks they the dose is increased to 4 mg. \* 2 daily. at four weeks all tests are readministered, as well as at six weeks. the study is concluded at 6 weeks, following a readministration of tests. physical examination is also administered at the conclusion.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
30
Inclusion Criteria
  • schizophrenia all types
  • 18>
Exclusion Criteria
  • uti
  • >65
  • non organic state
  • no depression treatment

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
sans, panss, hamilton, ham-a, calgary, physical examination, cogscan test
Secondary Outcome Measures
NameTimeMethod
esrs, progesterom, sexual functioning, covy, cgi, cgi improved

Trial Locations

Locations (1)

Abarbanel Medical Mental Health Center

🇮🇱

Bat Yam, Israel

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