NCT06758167

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
150

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2020

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
3.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 2, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 2, 2024

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

December 25, 2024

Completed
9 days until next milestone

First Posted

Study publicly available on registry

January 3, 2025

Completed
Last Updated

January 3, 2025

Status Verified

December 1, 2024

Enrollment Period

3.4 years

First QC Date

December 25, 2024

Last Update Submit

December 25, 2024

Conditions

Keywords

DepressionXingpiJieyu FormulaEscitalopramRelative EnergyElectroencephalogram

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

EXPERIMENTAL

Experimental group, treated with XingpiJieyu formula and escitalopram.

Drug: XingpiJieyu formulaDrug: Escitalopram

Placebo and escitalopram

PLACEBO COMPARATOR

Control group, treated with placebo and escitalopram.

Drug: PlaceboDrug: 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.

Also known as: XPJYF
XingpiJieyu formula

Placebo, no therapeutic effect.

Also known as: PLA
Placebo and escitalopram

A commonly used drug in MDD treatment.

Also known as: ESC
Placebo and escitalopramXingpiJieyu formula

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Location

MeSH Terms

Conditions

Depressive Disorder, MajorDepression

Interventions

Escitalopram

Condition Hierarchy (Ancestors)

Depressive DisorderMood DisordersMental DisordersBehavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

PropylaminesAminesOrganic ChemicalsNitrilesBenzofuransHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-RingHeterocyclic Compounds

Study Officials

  • Xueqin Wang, Doctor

    Peking University Sixth Hospital

    PRINCIPAL INVESTIGATOR

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

Locations