Placebo-controlled Trial of 5-hydroxytryptophan and Creatine for SSRI or SNRI Augmentation in Tre… (NCT02922725) | Clinical Trial Compass
TerminatedPhase 4
Placebo-controlled Trial of 5-hydroxytryptophan and Creatine for SSRI or SNRI Augmentation in Treatment Resistant Depression in Females
Stopped: COVID-19 pandemic
United States32 participantsStarted 2016-11
Plain-language summary
The investigators propose to determine if 8 weeks of dietary augmentation with oral 5g creatine monohydrate daily and 100 mg of 5-hydroxytryptophan (5-HTP) twice daily reduces hypoxia-related depressive symptoms measured by the 17-item Hamilton Depression Rating Scale (HAM-D) in women with SSRI- or SNRI-resistant depression, combined with the examination of changes in functional connectivity based on resting-state fMRI and changes in brain metabolism inferred from phosphorus-31 magnetic resonance spectroscopy.
Who can participate
Age range25 Years – 40 Years
SexFEMALE
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Female gender, ages 25-40 years inclusive
* Current diagnosis of Major Depressive Disorder identified by the SCID-I
* Current HAM-D17 score of \> 16
* Adequate adherence to any FDA approved SSRI or SNRI for at least 8 weeks
* Right-handed
Healthy Controls Inclusion criteria:
* Female gender, ages 25-40 inclusive
* No current or past DSM-5 diagnosis, as determined by clinical and structured interviews
Exclusion Criteria:
* Any non-MDD and non-anxiety psychiatric diagnosis, as identified by the SCID-I
* History of or current diagnosis of renal disease, such as chronic renal failure, acute renal failure or end stage renal disease
* Diabetes type I or II
* Current colitis or diverticulitis
* History of or current pulmonary disease
* History of cardiac disease or QTc \> 500ms
* History of fibromyalgia, lupus, eosinophilia-myalgia syndrome, dermatomyositis, polymyositis, rheumatoid arthritis, psoriatic arthritis, mixed connective tissue disease, ankylosing spondylitis, or other related rheumatological condition
* History of or current seizure disorder
* Current serious suicide risk identified by the Columbia Severity Suicide Rating Scale
* Current treatment with an antipsychotic, mood stabilizer, or non-SSRI antidepressant
* Positive pregnancy test, pregnancy, failure to use adequate birth control method
* Previous diagnosis of serotonin syndrome or evidence of serotonin syndrome
* Use of any excluded drugs or medications including serotonergic drugs or m…
What they're measuring
1
Change From Baseline in Hamilton Depression Rating Scale