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A Clinical Trial of Fluvoxamine for Melancholia

A Clinical Trial of Fluvoxamine for Melancholia

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04160377
Enrollment
150
Registered
2019-11-13
Start date
2019-08-01
Completion date
2022-09-30
Last updated
2022-04-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depressive Disorder, Endogenous Depression, Melancholia

Brief summary

This study aims at investigating the special effectiveness of antidepressant effect of Fluvoxamine for endogenous depression. The investigators also aim to assess the effect of Fluvoxamine on the multimodal magnetic resonance imaging(MRI), blood cytokines, feces bacteria flora and neuropsychological performance in depression patients with melancholic features. The investigators further aim to identify the predictors of Fluvoxamine's antidepressant effeect using the above techniques.

Detailed description

This study aims at investigating the special effectiveness of antidepressant effect of Fluvoxamine for melancholia. The investigators also aim to assess the effect of Fluvoxamine on the multimodal magnetic resonance imaging(MRI), blood cytokines, feces bacteria flora and neuropsychological performance in depression patients with melancholic features. The investigators further aim to identify the predictors of Fluvoxamine's antidepressant effeect using the above techniques.

Interventions

DRUGFluvoxamine

Fluvoxamine was assigned to be the treatment for the depression patients with melancholic features or not .

Sponsors

Lingjiang Li
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Adult (18-55 years, both sexes), with DSM-4 criteria for MDD without psychosis, as determined by a structured clinical interview Mini International Neuropsychiatric Interview * Moderate to severe depression, as defined by a pretreatment score ≥17 on the HDRS-17 scale * Informed consent to participate in this study * ethinic Han, right-handed, Junior high school education or above

Exclusion criteria

* A history of bipolar disorder, schizophrenia, schizoaffective disorder, obsessive-compulsive disorder, panic disorder, or documented Axis II diagnoses; active suicidal intention, as determined by clinical interview * Active or recent (\<12 months) substance abuse or dependence; excluding nicotine * Presence of ECT treatment in recent 6 months * period of pregnancy or lactation * hearing disorder or colour blindness * Immediate relatives have bipolar disorder or mania disorder

Design outcomes

Primary

MeasureTime frameDescription
Change in Hamilton Anxiety Rating Scale-14 item (HAMA-14)Baseline, 1 months, 2 monthsInterview-based questionnaire used to measure the severity of anxiety. Consists of 14 items with a score calculated. Higher scores are associated with more severe anxiety.
Change in Functional connectivityBaseline, 2 monthsChange in Functional connectivity of the brain networks as assessed by measure of connectivity in multimodal MRI.
Change in voxel-based morphometry of grey matter, white matter as assessed by structural magnetic resonancce imagingBaseline, 2 monthsParticipants will receive resting-state functional magnetic resonance imaging (MRI). Scans will be performed on a 3.0- T Siemens Magnetom Skyra scanner (Siemens Healthineers, Erlangen, Germany). During scanning, all participants were instructed to remain motionless, and to think of nothing in particular but to not fall asleep.
Change in Hamilton Depression Rating Scale-17 item (HAMD-17)Baseline, 2weeks, 1 months, 2 monthsInterview-based questionnaire used to measure the severity of depression. Consists of 17 items with a score calculated. Higher scores are associated with more severe depression.

Secondary

MeasureTime frameDescription
Change in DSST (Number of Correct Symbols)Baseline, 1 months, 2 monthsDigit Symbol Substitution Test (DSST) is a cognitive test designed to assess psychomotor speed of performance requiring visual perception, spatial decision-making, and motor skills. It consists of 133 digits and requires the patient to substitute each digit with a simple symbol in a 90-second period. Each correct symbol is counted, and the total score ranges from 0 (less than normal functioning) to 133 (greater than normal functioning). as a description of DSST.
Improvement on Snaith-Hamilton Pleasure Scale (SHAPS)Baseline, 1 months, 2 monthsThe Snaith-Hamilton Pleasure Scale (SHAPS) assesses the anhedonia symptoms of MDD patients, with higher score indicating more severe anhedonia. Evaluating the patient's pleasure experience and choosing the degree of agreement with the happy response in some pleasant situations, and each item was rated on a 4-point scale.1 = Strongly agree, 2 = agree, 3 = disagree and 4 = strongly disagree This scale evaluates the status of patients in the recent period of time, The total score of the scale is the sum of the scores of 14 items, with a total score of 14-56. The higher the total score, the more serious the anhedonia.
Young Manic Rating Scale (YMSR)Baseline, 1 months, 2 monthsThe YMSR assesses the manic symptoms of the subjects.
Life Event Scale (LES)Baseline, 1 months, 2 monthsThe LES assesses the effects of some life events on the subjects.
Beck Scale for Suicide Ideation(BSI)Baseline, 1 months, 2 monthsThe BSI assesses the Suicide Ideation of the subjects, including two time points, the latest week and when the subjects were the most depressive.
Hopkins Vocabulary Learning Test-Revised (HVLT-R)Baseline, 1 months, 2 monthsThe HVLT-R assesses the memory and the cognition of the subjects.
Sydney Melancholia Prototype Index (SMPI)Baseline, 1 months, 2 monthsThe SMPI aims to identify the melancholic and non-melancholic depression.
Self-reported Quick Inventory of Depressive Symptomatology (QIDS-SR) ScaleBaseline, 1 months, 2 monthsThe QIDS-SR assesses the depressive symtoms in latest week of subjects quickly.
Dimensional Anhedonia Rating Scale (DARS)Baseline, 1 months, 2 monthsThe DARS assesses different dimensions in Anhedonia of the subjects.
Child Trauma Scale (CTQ)Baseline, 1 months, 2 monthsThe CTQ assesses child trauma happen to the subjects.
Sheehan Disability Scale (SDS)Baseline, 1 months, 2 monthsThe SDS assesses the impairment in the occupational, familial and social ability of the subjects.
Pittsburgh Sleep Quality Index (PSQI)Baseline, 1 months, 2 monthsThe PSQI assesses the sleep quality of the subjects.
Perceived Deficit Questionnaire for Depression (PDQ-D)Baseline, 1 months, 2 monthsThe PDQ-D assesses the perceived deficit of the subjects
Medication Adherence Rating Scale (MARS)1 months, 2 monthsThe MARS assesses the medication adherence condition of the subjects
Rating Scale for Side Effects (SERS)1 months, 2 monthsThe SERS assesses the side effects of medication condition in the subjects
Generalized Anxiety Disoder-7 (GAD-7)Baseline, 1 months, 2 monthsThe GAD-7 aims to assesses the severity of anxious symtoms.
Change in peripheral blood cytokinesBaseline, 1 months, 2 monthsPeripheral blood sample will be collected and the concentration of IL-6, TNF-α, and CRP will be assessed.
Change in feces bacterial floraBaseline, 1 months, 2 monthsThe objective of investigator is to characterize gut microbiome in patients with TRD. To explore the specific diversity of gut microbiome. The stool samples were collected in the collection kits at the baseline, and were frozen at -80 °C. After the process of DNA Purification, 16S rRNA Gene Amplification and Illumina MiSeq sequencing, the study finally find the abundance and diversity of microbiota.
Change in Congruent STROOP Time to Complete (Executive Function)Baseline, 1 months, 2 monthsStroop Colour Naming Test (STROOP) is a cognitive test designed to assess the ability to inhibit a prepotent response to reading words while performing a task that requires attention control. It comprises two sheets with 50 words on each, and each word is the name of a colour. On the first sheet, the Congruent STROOP Sheet, the word and ink colour match; on the Incongruent STROOP Sheet, the word and ink colour do not match. For each sheet, the patient has 4 minutes to name the ink colour of each word. When the patient finishes the sheet, or once 4 minutes is up, the clinician notes the time taken and counts the number of correct and incorrect responses. The scale ranges from 0-100, the higher score the greater the cognitive flexibility.

Other

MeasureTime frameDescription
Halstead-Reitan neuropsychological test battery for adults(HRB)Baseline, 1 months, 2 monthsHalstead-Reitan neuropsychological test battery for adults assesses the basic functions of the brain,including perception, orientation, attention, action speed and memory.
Electroencephalogram (EEG)Baseline, 2 weeksEEG Microstate Parameters data likeECG QT Interval or EEG power in the alpha band, etc., were collected at a 5000 Hz sampling rate, using a 64-channel Ag-Cl electrode (Brain Products) for both resting-state and task-state.
Wechsler Scale (Digital Span)Baseline, 1 months, 2 monthsWechsler Scale (Digital Span) assesses the Attention and short-term memory of the subjects.

Countries

China

Contacts

Primary ContactXueqin Li
876659651@qq.com0086-15015102836

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026