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Integral Assessment in Unipolar Depression (AIUNI)

Primary Purpose

Major Depressive Disorder

Status
Unknown status
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Sertraline
Sponsored by
University of Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Major Depressive Disorder focused on measuring Early Improvement, Depression, Antidepressant

Eligibility Criteria

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

Inclusion Criteria:

  • Patients Presenting Depressive Episode according to DSM-IV-TR

Exclusion Criteria:

  • Patients presenting: psychotic symptoms, Axis 1 comorbidities (except specific phobia, specific social phobia and nicotine dependence) or risk of suicide (defined as score = 3 on item 3 of the 17-item HAMD or at the discretion of rater);
  • Other exclusion criteria are having a serious or unstable medical condition, including cardiovascular, hepatic, endocrinologic, neurological or renal conditions.
  • Clinically significant abnormalities on laboratory or ECG exams or those which, in the investigator ́s opinion, indicate a serious medical issue, require a major intervention or may interfere in the antidepressant treatment, also constitute grounds for exclusion.

Sites / Locations

  • Insitute of Psychiatry of the University of São PauloRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Sertraline

Arm Description

Patients using Sertraline with any dose will be evaluated about Early Improvement

Outcomes

Primary Outcome Measures

Early Improvement
20% reduction of baseline score on the Hamilton Depression Scale (HAMD-17)

Secondary Outcome Measures

Response
50% reductions of baseline score on the Hamilton Depression Scale (HAMD-17)
Remission
Score less than 7 points on the Hamilton Depression Scale (HAMD-17)

Full Information

First Posted
October 8, 2014
Last Updated
December 10, 2015
Sponsor
University of Sao Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT02268487
Brief Title
Integral Assessment in Unipolar Depression
Acronym
AIUNI
Official Title
THE AIUNI - Integral Assessment in Unipolar Depression
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Unknown status
Study Start Date
January 2014 (undefined)
Primary Completion Date
January 2017 (Anticipated)
Study Completion Date
January 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of this project is to assess the occurrence of early improvement within the first two weeks of antidepressant treatment and to correlate this improvement with favorable therapeutic outcome at the end of the acute and treatment continuation phases (8 and 24 weeks, respectively).
Detailed Description
An ongoing debate, as long-running as treatment with antidepressants itself, is the delay in response to these drugs. Antidepressant drugs take 2 to 4 weeks to produce the treatment response effect (at least 50% improvement in depressive symptoms versus baseline levels). This delay in antidepressant response can prove highly problematic since, during this interim period, the patient is exposed to the suffering, debilitative effects, direct and indirect costs and risks associated with major depressive disorder (MDD). Another important issue is when to define failure of a therapeutic trial and how to change treatment. Between 30 and 50% of MDD patients fail to respond to adequate first-line treatment. If favorable outcome is defined as full remission (as opposed to only 50% improvement) of the patient, the failure rate during first trial is greater still. Some reviews recommend dose adjustments every two weeks and a 4-8 week wait before treatment change for poor response. Despite these recommendations, the question over when and how to change treatment strategy warrants further debate. Early improvement in antidepressant treatment is desirable because it reduces the suffering, losses and costs associated with MDD. In addition, the risk of suicidal ideation or committing suicide are reduced in patients presenting early improvement of depressive symptoms. However, early improvement not only reduces risk but also predicts outcome at the end of the acute phase of treatment. A number of studies investigating different antidepressants have shown that the presence of early response is a good predictor of favorable outcome at the end of the acute phase of treatment (after 6 or 8 weeks of treatment). A meta-analysis reviewing 41 simple or double-blind clinical trials included a total of 6562 patients. Early improvement, defined as a 20% reduction in score on the Hamilton Depression Scale (HAMD-17) within 2 weeks, was associated with sustained response, remission (defined as HAM-D-17 score ≤7). While early response has been amply demonstrated in numerous clinical trials, there are gaps in knowledge on the subject. Scant studies have documented whether there are differences in the pattern of early improvement among different antidepressants. Similarly, there is a dearth of studies analyzing whether the presence or otherwise of early response has the same predictive value for different antidepressants. Another little explored aspect is the arbitrary nature of the criteria defining onset of improvement, early improvement, treatment response and symptomatological remission. Studies tend to reproduce previously-adopted criteria without elaborating on the exploratory analyses justifying the cut-off points adopted. The aim of the present study is to assess the presence of early improvement after one and two weeks of treatment with sertraline. Besides assessing the presence of early response, the study will include an exploratory analysis assessing positive and negative predictive values, sensitivity and specificity of early improvement as a predictor of sustained response and remission after 6, 8 and 24 weeks of treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder
Keywords
Early Improvement, Depression, Antidepressant

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sertraline
Arm Type
Experimental
Arm Description
Patients using Sertraline with any dose will be evaluated about Early Improvement
Intervention Type
Drug
Intervention Name(s)
Sertraline
Other Intervention Name(s)
Early Improvement
Intervention Description
Treatment
Primary Outcome Measure Information:
Title
Early Improvement
Description
20% reduction of baseline score on the Hamilton Depression Scale (HAMD-17)
Time Frame
2 Weeks
Secondary Outcome Measure Information:
Title
Response
Description
50% reductions of baseline score on the Hamilton Depression Scale (HAMD-17)
Time Frame
4 and 8 weeks
Title
Remission
Description
Score less than 7 points on the Hamilton Depression Scale (HAMD-17)
Time Frame
8 and 24 weeks

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: Patients Presenting Depressive Episode according to DSM-IV-TR Exclusion Criteria: Patients presenting: psychotic symptoms, Axis 1 comorbidities (except specific phobia, specific social phobia and nicotine dependence) or risk of suicide (defined as score = 3 on item 3 of the 17-item HAMD or at the discretion of rater); Other exclusion criteria are having a serious or unstable medical condition, including cardiovascular, hepatic, endocrinologic, neurological or renal conditions. Clinically significant abnormalities on laboratory or ECG exams or those which, in the investigator ́s opinion, indicate a serious medical issue, require a major intervention or may interfere in the antidepressant treatment, also constitute grounds for exclusion.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fernando Fernandes, MD
Phone
+55 11 997810107
Email
fernandes2000@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Moreno A Ricardo, PhD
Phone
+55 11 2661 2866
Email
gmissio@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Moreno A Ricardo, PhD
Organizational Affiliation
University of São Paulo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Insitute of Psychiatry of the University of São Paulo
City
São Paulo
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fernando Fernandes, MD
Phone
+55 11 997810107
Email
fernandes2000@gmail.com
First Name & Middle Initial & Last Name & Degree
Ricardo A Moreno, Dr
Email
gmissio@gmail.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
16415707
Citation
Papakostas GI, Perlis RH, Scalia MJ, Petersen TJ, Fava M. A meta-analysis of early sustained response rates between antidepressants and placebo for the treatment of major depressive disorder. J Clin Psychopharmacol. 2006 Feb;26(1):56-60. doi: 10.1097/01.jcp.0000195042.62724.76.
Results Reference
background
PubMed Identifier
11444762
Citation
Thase ME. Methodology to measure onset of action. J Clin Psychiatry. 2001;62 Suppl 15:18-21.
Results Reference
background
PubMed Identifier
19254516
Citation
Szegedi A, Jansen WT, van Willigenburg AP, van der Meulen E, Stassen HH, Thase ME. Early improvement in the first 2 weeks as a predictor of treatment outcome in patients with major depressive disorder: a meta-analysis including 6562 patients. J Clin Psychiatry. 2009 Mar;70(3):344-53. doi: 10.4088/jcp.07m03780. Epub 2009 Feb 24.
Results Reference
background

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Integral Assessment in Unipolar Depression

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