Depression Clinical Trial
Official title:
N-methylglycine (Sarcosine) for Treatment of Major Depressive Disorder
Major depressive disorder is a complex disease and most currently available antidepressants aiming at monoamine neurotransmission exhibit limited efficacy and cognitive effects. N-methyl-D-aspartate (NMDA), one subtype of glutamate receptors, plays an important role in learning and memory. N-methyl-D-aspartic acid (NMDA) enhancing agents, such as sarcosine (N-methylglycine), have been used as adjunctive therapy of schizophrenia. Sarcosine improved not only psychotic but also depressive symptoms in patients with schizophrenia. To confirm its antidepressant effect, the purpose of this study is to compare citalopram and sarcosine in efficacy for major depressive patients.
Major depressive disorder is a complex disease and most currently available antidepressants
aiming at monoamine neurotransmission exhibit limited efficacy and cognitive effects. Novel
therapies via manipulating other neurotransmission (e.g. glutamate receptor) are being
developed.
NMDA enhancing agents, such as sarcosine have been demonstrated to improve negative symptoms
and depressive symptoms of schizophrenic patients. The purpose of this study is to compare
citalopram and sarcosine in aspects of efficacy, safety in major depressive patients.
In the study, 40 major depressive patients are recruited into the 6-week trial and randomly
assigned into the two groups (20-60 mg/d citalopram, or 500 - 1500 mg/d sarcosine) with a
double-blind manner. Hamilton Depression Rating Scale(17-item), CGI(Clinical Global
Impression), GAF(Global Assessment of Function)and side effects are evaluated every two
weeks during the trial. The efficacies of two groups are compared.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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