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Reboxetine Adjuvant Therapy for the Treatment of Schizophrenia

Phase 1 Study of Reboxetine Adjuvant Therapy and Cognitive and Behavioral Measures

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00409201
Enrollment
30
Registered
2006-12-08
Start date
2006-03-31
Completion date
2006-11-30
Last updated
2006-12-08

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

Conditions

Schizophrenia

Keywords

schizophrenia, reboxetine, cognitive, behavior

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.

Interventions

DRUGreboxetine adjuvant therapy

Sponsors

Abarbanel Mental Health Center
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* schizophrenia all types * 18\>

Exclusion criteria

* uti * \>65 * non organic state * no depression treatment

Design outcomes

Primary

MeasureTime frame
sans, panss, hamilton, ham-a, calgary, physical examination, cogscan test

Secondary

MeasureTime frame
esrs, progesterom, sexual functioning, covy, cgi, cgi improved

Countries

Israel

Contacts

Primary Contactstanislav baranchik, md
972-3-5552625

Outcome results

None listed

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