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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04101474
Other study ID # Ketamine with TRD
Secondary ID
Status Not yet recruiting
Phase Early Phase 1
First received
Last updated
Start date December 1, 2019
Est. completion date February 1, 2021

Study information

Verified date September 2019
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study we will assess the effect of Ketamine infusion on depressive symptoms and in particular its effect on Suicidal behavior, ideation and thoughts in patients with treatment- resistant MDD.


Description:

A Twice repetition of IV infusion of 0.5 mg/kg of ketamine produces an antidepressant response in individuals with treatment-resistant MDD

The work aims to:

1. To assess the onset of action and degree of improvement and the duration of antidepressant effect of ketamine in a sample of patients with treatment -resistant major depressive disorder.

2. To find out whether the onset of Ketamine antidepressant effect is associated with an improvement of suicidality in those patients.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date February 1, 2021
Est. primary completion date December 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Patients fulfilling diagnostic criteria of treatment-resistant MDD.

2. Presence of suicidal risk.

3. No comorbid medical or neurological conditions.

4. Age above 18 years old.

5. Both gender.

6. Informed written consent from the patient or his legitimate.

Exclusion Criteria:

1. Presence of perceptual disturbance.

2. History of sensitivity to ketamine.

3. Refusal to participate in the study.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ketamine
Ketamine is a high-affinity, noncompetitive N-methyl-D- aspartate (NMDA) glutamate receptor antagonist it has been used in anesthesiology for more than 50 years the time course of antidepressant response to ketamine is characterized by an initial reduction in depressive symptoms within 2 h

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary Role of Ketamine as Antidepressant the onset of action and degree of improvement and the duration of antidepressant effect of ketamine in a sample of patients with treatment -resistant major depressive disorder. 1 year
Primary Effect of Ketamine on Suicidality finding out whether the onset of Ketamine antidepressant effect is associated with an improvement of suicidality in those patients 1 year
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