Protocol summary

Study aim
Investigating the effect of Lumateperone as adjuvant therapy to sertraline in major depressive disorder
Design
Randomized double blind and placebo-controlled clinical trial
Settings and conduct
This study will be performed on patients with MDD attending Roozbeh Hospital
Participants/Inclusion and exclusion criteria
Inclusion criteria: Based on DSM-V have a diagnosis of major depression (MDD) and their minimum severity of depression based on HDRS is 19 Age between 18-65. Exclusion criteria: Any other mental disorder in another axis - Serious suicidal thoughts (<2 in suicidal HDRS section) - Psychosis - History of ECT in recent two months - History of mania and hypomania - Thyroid dysfunctions - History of cardiovascular disease - Diabetes - Autoimmune disorders - Presence of active infection - Neurologic disorders like epilepsy and Alzheimer's disease - Liver disease - Kidney disease - Pregnant or lactating women.
Intervention groups
Intervention group received sertraline at a dose of 100 mg / day, and Lumateperone at a dose of 42 mg / day, and the control group received sertraline at a dose of 100 mg / day and placebo. Patients at weeks 0, 2, 4, and 8 will be evaluated by the HDRS. Neuropsychiatric assessments are applied at baseline (first visit) and final (eighth week). Finally, side effects at each visit are assessed using a 25-item questionnaire (Systematic Assessment for Treatment Emergent Effects).
Main outcome variables
Severity of depression

General information

Reason for update
Acronym
IRCT registration information
IRCT registration number: IRCT20090117001556N141
Registration date: 2022-03-01, 1400/12/10
Registration timing: prospective

Last update: 2022-03-01, 1400/12/10
Update count: 0
Registration date
2022-03-01, 1400/12/10
Registrant information
Name
Shahin Akhondzadeh
Name of organization / entity
Roozbeh Psychiatric Hospital, Tehran University of Medical Sciences
Country
Iran (Islamic Republic of)
Phone
+98 21 5541 2222
Email address
s.akhond@sina.tums.ac.ir
Recruitment status
Recruitment complete
Funding source
Expected recruitment start date
2022-04-21, 1401/02/01
Expected recruitment end date
2024-04-20, 1403/02/01
Actual recruitment start date
empty
Actual recruitment end date
empty
Trial completion date
empty
Scientific title
Lumateperone as adjuvant therapy to sertraline in major depressive disorder: A randomized double blind and placebo controlled clinical trial
Public title
Lumateperone as adjuvant therapy for major depressive disorder
Purpose
Treatment
Inclusion/Exclusion criteria
Inclusion criteria:
Based on DSM-V have a diagnosis of major depression (MDD) and their minimum severity of depression based on HDRS is 19 Age between 18-65
Exclusion criteria:
Any other mental disorder in another axis Serious suicidal thoughts (<2 in suicidal HDRS section) Psychosis History of ECT in recent two months History of mania and hypomania Thyroid dysfunctions History of cardiovascular disease Diabetes Autoimmune disorders Presence of active infection Neurologic disorders like epilepsy and Alzheimer's disease Liver disease Kidney disease Pregnant or lactating women
Age
From 18 years old to 65 years old
Gender
Both
Phase
2-3
Groups that have been masked
  • Participant
  • Care provider
  • Outcome assessor
Sample size
Target sample size: 50
Randomization (investigator's opinion)
Randomized
Randomization description
Permuted block randomization: using A and B blocks with n=4; AABB, ABAB, ABBA, BABA, BAAB, BBAA. We randomly use the blocks to achieve total sample size. ("A" and "B" are the study groups).
Blinding (investigator's opinion)
Double blinded
Blinding description
The participants, care providers and outcome assessors will be blind regarding grouping. All the participants believe that they are taking the main medication (the participants who are taking placebo are not aware of it). Care providers and outcome assessors do not know which participants have received the main medication and which participants have received placebo. Thus, there is no orientation in their work process.
Placebo
Used
Assignment
Parallel
Other design features

Secondary Ids

empty

Ethics committees

1

Ethics committee
Name of ethics committee
Ethics Committee of Tehran University of Medical Sciences
Street address
Tehran University of Medical Sciences, Qhods St., Keshavarz Blvd.
City
Tehran
Province
Tehran
Postal code
1417653761
Approval date
2021-12-05, 1400/09/14
Ethics committee reference number
IR.TUMS.DDRI.REC.1400.048

Health conditions studied

1

Description of health condition studied
Major depressive disorder
ICD-10 code
F32
ICD-10 code description
Major depressive disorder, single episode

Primary outcomes

1

Description
Severity of depression
Timepoint
Weeks 0 - 4 - 8
Method of measurement
by Hamiltion Depression Rating Scale

Secondary outcomes

empty

Intervention groups

1

Description
Intervention group: received sertraline at a dose of 100 mg / day, and Lumateperone at a dose of 42 mg / day for 8 weeks.
Category
Treatment - Drugs

2

Description
Control group: received sertraline at a dose of 100 mg / day and placebo.
Category
Placebo

Recruitment centers

1

Recruitment center
Name of recruitment center
Roozbeh hospital
Full name of responsible person
Dr. Mohammad Reza Mohammadi
Street address
Roozbeh Hospital, South Kargar Street, Tehran
City
Tehran
Province
Tehran
Postal code
1333715914
Phone
+98 21 5541 2222
Email
mohammadimr@tums.ac.ir

Sponsors / Funding sources

1

Sponsor
Name of organization / entity
Tehran University of Medical Sciences
Full name of responsible person
Dr..Akbar Fotouhi
Street address
Tehran University of Medical Sciences, Qhods St., Keshavarz Blvd.
City
Tehran
Province
Tehran
Postal code
1417653761
Phone
+98 21 8898 7381
Email
afotouhi@tums.ac.ir
Grant name
Grant code / Reference number
Is the source of funding the same sponsor organization/entity?
No
Title of funding source
Tehran University of Medical Sciences
Proportion provided by this source
100
Public or private sector
Public
Domestic or foreign origin
Domestic
Category of foreign source of funding
empty
Country of origin
Type of organization providing the funding
Academic

Person responsible for general inquiries

Contact
Name of organization / entity
Tehran University of Medical Sciences
Full name of responsible person
Dr. Shahin Akhondzadeh
Position
Professor of clinical psychopharmacology
Latest degree
Ph.D.
Other areas of specialty/work
Medical Pharmacy
Street address
Roozbeh Hospital, South Kargar Street, Tehran
City
Tehran
Province
Tehran
Postal code
1333715914
Phone
+98 21 5541 2222
Email
s.akhond@sina.tums.ac.ir

Person responsible for scientific inquiries

Contact
Name of organization / entity
Tehran University of Medical Sciences
Full name of responsible person
Dr. Shahin Akhondzadeh
Position
Professor of clinical psychopharmacology
Latest degree
Ph.D.
Other areas of specialty/work
Medical Pharmacy
Street address
Roozbeh Hospital, South Kargar Street, Tehran
City
Tehran
Province
Tehran
Postal code
1333715914
Phone
+98 21 5541 2222
Email
s.akhond@sina.tums.ac.ir

Person responsible for updating data

Contact
Name of organization / entity
Tehran University of Medical Sciences
Full name of responsible person
Dr. Shahin Akhondzadeh
Position
Professor of clinical psychopharmacology
Latest degree
Ph.D.
Other areas of specialty/work
Medical Pharmacy
Street address
Roozbeh Hospital, South Kargar Street, Tehran
City
Tehran
Province
Tehran
Postal code
1333715914
Phone
+98 21 5541 2222
Email
s.akhond@sina.tums.ac.ir

Sharing plan

Deidentified Individual Participant Data Set (IPD)
Yes - There is a plan to make this available
Study Protocol
Yes - There is a plan to make this available
Statistical Analysis Plan
Yes - There is a plan to make this available
Informed Consent Form
Yes - There is a plan to make this available
Clinical Study Report
Yes - There is a plan to make this available
Analytic Code
Yes - There is a plan to make this available
Data Dictionary
No - There is not a plan to make this available
Title and more details about the data/document
The data will be distributed through final report
When the data will become available and for how long
5 years from 2022 to 2027
To whom data/document is available
academic researchers
Under which criteria data/document could be used
users should cite the resource of data
From where data/document is obtainable
Prof Shahin Akhondzadeh
What processes are involved for a request to access data/document
by E mail
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