RCT Study on the Therapeutic Effect of Escitalopram Loaded With XingpiJieyu Formula on Resting State EEG Energy Abnormalities in Severe Liver Depression and Spleen Deficiency Type MDD
1 other identifier
interventional
150
1 country
1
Brief Summary
To compare the clinical efficacy of XingpiJieyu formula or its placebo combined with Escitalopram (ESC) in the treatment of moderate and severe MDD, and to explore a new method of integrated traditional Chinese and western medicine for the treatment of moderate and severe MDD with severe liver depression and spleen deficiency, as well as its neurological mechanism for regulating the relative power (RP) of resting-state EEG spectra.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Nov 2020
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 14, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 2, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
April 2, 2024
CompletedFirst Submitted
Initial submission to the registry
December 25, 2024
CompletedFirst Posted
Study publicly available on registry
January 3, 2025
CompletedJanuary 3, 2025
December 1, 2024
3.4 years
December 25, 2024
December 25, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
17-item Hamilton Depression Scale (HAMD-17)
The Hamilton Depression Scale (HAMD) was developed by Hamilton in 1960 and is the most commonly used scale for clinical assessment of depressive states. This scale is used by two trained raters to conduct a combined HAMD examination of the patient, usually in the form of conversation and observation, and at the end of the examination, the two raters rate independently; by using this scale, the severity of the condition and the effectiveness of the treatment can be evaluated.
8 weeks
Hamilton Anxiety Scale (HAMA)
Hamilton Anxiety Scale (HAMA), compiled by Hamilton in 1959, is one of the commonly used scales in psychiatric clinics, and the total score of HAMA can better reflect the severity of anxiety symptoms, which can be used to evaluate the severity of anxiety symptoms in patients with anxiety and depression disorders and to assess the effects of various medications and psychological interventions.
8 weeks
Health Questionnaire-15 (PHQ-15)
The Patient Health Questionnaire-15 (PHQ-15) is a scale used to assess an individual's somatic symptoms and dysfunction. It consists of 15 common somatic symptom items, and assesses a person's somatic health status by asking the participant to select the symptoms that correspond to his or her condition. The scale can be used to screen and assess the presence and severity of clusters of somatic symptoms, helping healthcare professionals to quickly understand a patient's somatic health problems.
8 weeks
Pittsburgh sleep quality index (PSQI)
The Pittsburgh sleep quality index (PSQI) was compiled in 1989 by Dr Buysse, a psychiatrist at the University of Pittsburgh, USA, and others. The scale is suitable for patients with sleep disorders and patients with psychiatric disorders to evaluate the quality of sleep, but also for the general population to assess the quality of sleep.
8 weeks
Treatment Emergent Symptom Scale (TESS)
The Side Effects Scale (TESS) is a tool used to assess side effects of medications. It rates side effects in different categories to determine the extent to which a drug is causing side effects in a patient and whether adjustments to the treatment regimen are needed. It can help physicians better understand the side effects of medications and make timely adjustments to treatment regimens to improve outcomes and reduce adverse reactions in patients.
8 weeks
Study Arms (2)
XingpiJieyu formula
EXPERIMENTALExperimental group, treated with XingpiJieyu formula and escitalopram.
Placebo and escitalopram
PLACEBO COMPARATORControl group, treated with placebo and escitalopram.
Interventions
XingpiJieyu formula is a traditional Chinese medicine. It pays attention to the regulation of qi and blood. Previous studies have shown that its clinical effect of treating mild and moderate depression is significant, for example, it can effectively improve depressive mood and somatic symptoms, and increase peripheral blood ATP levels in patients with depression.
A commonly used drug in MDD treatment.
Eligibility Criteria
You may qualify if:
- outpatient/inpatient, age 18-45 years old, right-handed;
- western medical diagnosis meets the diagnostic criteria of MDD in DSM-5, without psychiatric features;
- In accordance with the diagnostic criteria of depression and liver-stagnation and spleen-deficiency in the "Guidelines for Diagnosis and Treatment of Internal Diseases in Traditional Chinese Medicine" issued by the China Association of Chinese Medicine in 2008;
- item Hamilton Depression Scale score ≥18;
- educational experience ≥5 years;
- The current episode has not used antidepressants, antipsychotics, mood stabilizers, or other medications that can act on the central nervous system for at least 4 weeks;
- Have not received physical therapy, such as MECT, rTMS, etc., in the past 6 months;
- The total duration of the disease ≤10 years.
You may not qualify if:
- Any current or previous mental disorder other than MDD according to DSM-5;
- Diagnosis of syndromes other than depression and liver-stagnation and spleen-deficiency in the "Guidelines for Diagnosis and Treatment of Internal Diseases in Traditional Chinese Medicine" issued by the China Association of Chinese Medicine in 2008;
- Suicidal ideation or suicidal behaviour (HAMD-17 item 3 \> 2);
- Drinking alcohol in the week prior to the enrollment;
- Patients with neurological disorders, somatic disorders, organic brain diseases, and tumour;
- Sleep disorders other than insomnia disorders currently diagnosed according to DSM-5, such as obstructive sleep apnea syndrome, periodic limb movement disorder, restless legs syndrome, etc.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Peking University Sixth Hospital
Beijing, Beijing Municipality, 100191, China
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Xueqin Wang, Doctor
Peking University Sixth Hospital
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
December 25, 2024
First Posted
January 3, 2025
Study Start
November 14, 2020
Primary Completion
April 2, 2024
Study Completion
April 2, 2024
Last Updated
January 3, 2025
Record last verified: 2024-12
Data Sharing
- IPD Sharing
- Will not share