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Ketamine for Treatment Resistant MDD

Primary Purpose

Depressive Disorder, Major

Status
Unknown status
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Ketamine
Sponsored by
Hadassah Medical Organization
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depressive Disorder, Major

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosed with unipolar/bipolar depression with MADRS Score>= 20
  • Inadequate response to >= 3 adequate treatment trials [>=2 trials in the present episode]
  • If on psychopharmacological Tx, it should be stable since 4 weeks prior to enrollment
  • QTc WNL

Exclusion Criteria:

  • Hypersensitivity to ketamine
  • Other major psychiatric diagnosis
  • High suicidality
  • Unstable physical illness
  • S/P CVA / brain SOL
  • Pregnant or breast feeding women
  • Illicit drug/alcohol abuse during last year
  • History of ketamine abuse

Sites / Locations

  • Hadassah Hebrew University Medical CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

MDD

Arm Description

Treatment resistant patients will be treated with multiple doses of IM/SC ketamine [dose range 0.3-1.5mg/kg]

Outcomes

Primary Outcome Measures

MADRS
The change in the MDRS score at 1 month (5weeks evaluation) for the acute phase and at 6 months or end of study (for the maintenance phase) compared to baseline

Secondary Outcome Measures

MADRS
The change in MADRS score at 3 months compared to baseline.
QIDS-SR, Clinical Global Impressions - Improvement
The change in QIDS-SR and CGI scores at 1, 3 and 6 months compared to baseline.
Average time in remission
Average time in remission.
NeuroTrax computerized cognitive battery
Changes in cognitive function at 1 and 6 months [or at study end] as assessed by the NeuroTrax computerized cognitive battery compared to baseline. correlation between information processing speed and other cognitive domains at baseline and clinical outcomes.

Full Information

First Posted
July 10, 2019
Last Updated
July 15, 2019
Sponsor
Hadassah Medical Organization
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1. Study Identification

Unique Protocol Identification Number
NCT04021433
Brief Title
Ketamine for Treatment Resistant MDD
Official Title
Ketamine for Treatment Resistant Depression - A Long Term Feasibility Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2019
Overall Recruitment Status
Unknown status
Study Start Date
September 1, 2018 (Actual)
Primary Completion Date
October 1, 2020 (Anticipated)
Study Completion Date
December 30, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hadassah Medical Organization

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study aims to openly test the long-term safety, tolerability and effectiveness of repeated administration of IM/SC ketamine for treatment resistant MDD.
Detailed Description
Major depression disorder (MDD) is a common psychiatric disorders with considerable impact on patients' quality of life, social and occupational function. MDD also significantly increase suicide rate. About a third of the patients with MDD suffer from moderate to severe symptoms that are fully or partially unresponsive to accepted pharmaco and / or psycho therapy. Ketamine is a widely used anesthetic. Multiple studies done over the recent years had shown its therapeutic effects in resistant depressive patients. Unlike regular antidepressants, ketamine exerts its effect within hours to few days which implies an alternative mechanism of action not fully studied. So far, there are only few reports on using repeated ketamine administration to maintain the antidepressant effect or on intra-muscular or sub-cutaneous application that can be safer and more tolerable than the intravenous route. In the present study, the investigators aim to openly assess the safety, tolerability and effectiveness of repeated, individually tailored IM or SC ketamine for treatment resistant major depression. The investigators intend to explore questions regarding optimal dose, treatment frequency and duration. The investigators will also assess potential cognitive effects of long-term ketamine treatment and look for possible treatment outcome predictors using the Neurotrax computerized cognitive battery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depressive Disorder, Major

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
open
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MDD
Arm Type
Experimental
Arm Description
Treatment resistant patients will be treated with multiple doses of IM/SC ketamine [dose range 0.3-1.5mg/kg]
Intervention Type
Drug
Intervention Name(s)
Ketamine
Intervention Description
Repeated doses of IM/SC ketamine up to 3 times a week
Primary Outcome Measure Information:
Title
MADRS
Description
The change in the MDRS score at 1 month (5weeks evaluation) for the acute phase and at 6 months or end of study (for the maintenance phase) compared to baseline
Time Frame
1 month into treatment through study completion
Secondary Outcome Measure Information:
Title
MADRS
Description
The change in MADRS score at 3 months compared to baseline.
Time Frame
3 months into treatment
Title
QIDS-SR, Clinical Global Impressions - Improvement
Description
The change in QIDS-SR and CGI scores at 1, 3 and 6 months compared to baseline.
Time Frame
along 6 months
Title
Average time in remission
Description
Average time in remission.
Time Frame
along 6 months
Title
NeuroTrax computerized cognitive battery
Description
Changes in cognitive function at 1 and 6 months [or at study end] as assessed by the NeuroTrax computerized cognitive battery compared to baseline. correlation between information processing speed and other cognitive domains at baseline and clinical outcomes.
Time Frame
along 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed with unipolar/bipolar depression with MADRS Score>= 20 Inadequate response to >= 3 adequate treatment trials [>=2 trials in the present episode] If on psychopharmacological Tx, it should be stable since 4 weeks prior to enrollment QTc WNL Exclusion Criteria: Hypersensitivity to ketamine Other major psychiatric diagnosis High suicidality Unstable physical illness S/P CVA / brain SOL Pregnant or breast feeding women Illicit drug/alcohol abuse during last year History of ketamine abuse
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Moshe Isserles, MD
Phone
00972 2 6777184
Email
moshay@hadassah.org.il
First Name & Middle Initial & Last Name or Official Title & Degree
Hadas Lamberg, PhD
Phone
00 972 2 6777572
Email
lhadas@hadassah.org.il
Facility Information:
Facility Name
Hadassah Hebrew University Medical Center
City
Jerusalem
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Isserles Moshe, MD, MSc

12. IPD Sharing Statement

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Ketamine for Treatment Resistant MDD

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