Major Depressive Disorder Clinical Trial
Official title:
THE AIUNI - Integral Assessment in Unipolar Depression
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).
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.
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Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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