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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04238039
Other study ID # 5826-18-SMC
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 14, 2019
Est. completion date April 1, 2020

Study information

Verified date January 2020
Source The Chaim Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial 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.


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 information / eligibility

Status Recruiting
Enrollment 16
Est. completion date April 1, 2020
Est. primary completion date February 1, 2020
Accepts healthy volunteers No
Gender All
Age group N/A to 90 Years
Eligibility Inclusion Criteria:

- Participants in the ketamine study

Exclusion Criteria:

-

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Revital Amiaz Ramat Gan RI

Sponsors (1)

Lead Sponsor Collaborator
The Chaim Sheba Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time to relapse Medications 5 years