MedPath

Ketamine Long Therm Follow Up Study

Conditions
Followin Ketamine Treatment
Registration Number
NCT04238039
Lead Sponsor
The Chaim Sheba Medical Center
Brief Summary

Results of the study and of 5 years follow up of depressed patients who participated in the study during 2014-2015. We will locate the participants and will interview them will use the same questionnaires to evaluate their depressive symptoms. We will also measure the time to relapse.

Detailed Description

Anamnestic data will be collected from the patients, in addition, depressive symptoms will be measured using Montgomery Asberg Depression Scale (MADRAS). In addition, the Clinical Global Severity Scale (CGI-S) and Clinical Global Improvement (CGI-I) were performed 2 hours after treatment. In addition, we performed to prolong the time to relapse in this patient.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
16
Inclusion Criteria
  • Participants in the ketamine study
Exclusion Criteria

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time to relapse5 years

Medications

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Revital Amiaz

🇮🇱

Ramat Gan, RI, Israel

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