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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00294944
Other study ID # SHEBA-05-3911-JZ-CTIL
Secondary ID
Status Withdrawn
Phase Phase 3
First received February 19, 2006
Last updated January 28, 2008

Study information

Verified date January 2008
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

Assessing the effectiveness of Idazoxan as a treatment for depressive patients who did not respond to treatment with SSRI


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- MDD patients

- Did not respond to at least one treatment of 4-6 weeks of SSRI in adequate dose

- In or out patients

Exclusion Criteria:

- Psychotic symptoms

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind


Intervention

Drug:
Idazoxan


Locations

Country Name City State
Israel Chaim Sheba Medical Center Ramat-Gan

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

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