D-Cycloserine Augmentation of Intermittent Theta Burst Stimulation (iTBS) in Depression (COGENT)

Last updated: February 3, 2025
Sponsor: The Alfred
Overall Status: Active - Recruiting

Phase

2

Condition

Depression (Major/severe)

Depression

Mood Disorders

Treatment

D-Cycloserine

Intermittent Theta Burst Stimulation

Clinical Study ID

NCT05591677
567-22
  • Ages > 18
  • All Genders

Study Summary

The goal of this clinical trial is to investigate if the drug D-Cycloserine (DCS) improves the antidepressant effects of Intermittent Theta Burst Stimulation (iTBS), a non-invasive brain stimulation therapy, in patients with Major Depressive Disorder (MDD). The main questions it aims to answer are:

  • Whether taking DCS prior to iTBS therapy will be more effective in improving depressive symptoms than iTBS therapy alone.

  • Compare the effect of DCS 100mg/day versus 50mg/day on depressive symptoms.

  • Test the safety and tolerability of DCS. Participants will take either 50mg DCS per day, 100mg DCS or placebo prior to each iTBS treatment session. iTBS treatment will be administered daily, 5 days a week for 4 weeks. Clinical measures will be conducted at baseline and at the ends of weeks 1, 2, 3 and 4 of treatment.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Diagnosis of major depressive episode (MDE), in accordance with the Diagnostic andStatistical Manual of Mental Disorders 5th edition (DSM-5), in the context ofunipolar major depressive disorder or bipolar affective disorder.

  • 18 years or older in age.

  • Treatment resistant depression at Stage II of the Thase and Rush classification.56

  • Baseline Montgomery Åsberg Depression Rating Scale score of ≥ 20 (moderate-to-severedepression severity).57,58

  • No increase or initiation of new antidepressant therapy in the four weeks prior toscreening.

  • Demonstrated capacity to give informed consent.

Exclusion

Exclusion Criteria:

  • Inability to provide informed consent.

  • Medically unstable patients at the discretion of the investigator.

  • Concomitant neurological disorder or a history of a seizure disorder.

  • Participants who are pregnant.

  • Current substance use meeting DSM-5 criteria for substance use disorder.

  • Per DSM-5, had ever met diagnostic criteria for schizophrenia, schizoaffectivedisorder, schizophreniform disorder or delusional disorder as assessed by theMini-International Neuropsychiatric Interview (MINI) at the time of screening.

  • Diagnosis of any other mental disorder that is the participant's primary diagnosisor main mental health syndrome of concern at the time of screening, which maysignificantly affect psychiatric status and assessed as likely to impact trialparticipation, in the clinical judgement of the investigator.

Study Design

Total Participants: 180
Treatment Group(s): 2
Primary Treatment: D-Cycloserine
Phase: 2
Study Start date:
April 21, 2023
Estimated Completion Date:
December 31, 2025

Study Description

Major Depressive Disorder (MDD) is a common and debilitating condition with high rates of treatment resistance. Repetitive transcranial magnetic stimulation (rTMS) is an established treatment for treatment-resistant depression with few adverse effects. Intermittent Theta Burst Stimulation (iTBS) is a time-efficient form of rTMS with evidence base in the treatment of treatment-resistant depression (TRD). The most commonly supported understanding of iTBS's mechanism of action appear to be its strengthening of connections between networks of neurons, which is modulated by the N-methyl-D-aspartate (NMDA) receptor. D-cycloserine (DCS) is a partial NMDA receptor agonist that has demonstrable impact on rTMS and TBS's neuromodulatory effects. This study protocol proposes the conduct of a prospective multi-site, parallel-arm design, randomized, double-blinded, placebo-controlled clinical trial to investigate DCS augmentation of iTBS in MDD. We will investigate if adjuvant DCS 50mg or 100mg/day might have superior iTBS antidepressant augmentation effects.

Connect with a study center

  • Monash Alfred Psychiatry Research Centre

    Melbourne, Victoria 3004
    Australia

    Active - Recruiting

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