A Study of Xiongdan Wan Treating Depression

Last updated: April 16, 2024
Sponsor: Shanghai Mental Health Center
Overall Status: Completed

Phase

2

Condition

Depression

Depression (Adult And Geriatric)

Depression (Major/severe)

Treatment

Xiongdan Wan

Clinical Study ID

NCT05136365
SHXD2021CR2103B
  • Ages 18-65
  • All Genders

Study Summary

This is a prospective, single-arm, open-label study to evaluate the safety and efficacy of Xiongdan Wan monotherapy in patients with Major Depressive Disorder(MDD), conducted in Shang Hai Mental Health Center. Following a screening period, subjects who meet the entry criteria will be treated with 450mg Xiongdan Wan pills three times daily for 8 weeks.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Meets the Diagnostic and Statistical Manual of Mental Disorder, Fourth Edition TextRevision (DSM-IV-TR) criteria for Major Depressive Disorder (MDD): a single orrecurrent episode without psychotic features. Codes are as follows: F32.0, F32.1,F32.2, F33.0, F33.1, F33.2.
  2. Outpatients.
  3. Male or female subjects aged 18-65 years.
  4. HAMD-17 score of the baseline period and screening period is 18-24.
  5. Women of childbearing potential must be willing to use acceptable methods ofcontraception throughout the study period and the following one month.
  6. The patient fully understands and signs the informed consent form.

Exclusion

Exclusion Criteria:

  1. Patient has survived a suicide attempt or has acute suicidal tendencies (HAMD-17 Item3 ≥3).
  2. Comorbidity according to DSM-IV-TR, axis-I except for major depressive disorder.
  3. HAMD-17 reduction ratio ≥25% within one week from the screening to the baselineperiod.
  4. Depressive episode secondary to psychiatric illness or somatic disease.
  5. Serious and unstable diseases such as cerebrovascular disease; liver and kidneydisease; disease of internal secretion (abnormal thyroid function); hemopathy;seizures, or other encephalopathies.
  6. History of alcohol or drug abuse over the last 6 months.
  7. Allergic history to Xiongdan Wan, or serious drug allergic history.
  8. Pregnant or lactating women and women of childbearing potential throughout the studyperiod; men who have the desire of fertility within six months.
  9. Clinically significant changes in ECG or laboratory tests, including >1.5 times theupper limit of normal liver function; over the limit of normal renal function andblood sugar; abnormal cardiac troponins; obvious abnormity in the thyroid function.
  10. Treatment with modified electroconvulsive therapy (MECT) or repetitive transcranialmagnetic stimulation (rTMS) in the past three months.
  11. Treatment with a systematic psychological treatment in the past three months.

Study Design

Total Participants: 30
Treatment Group(s): 1
Primary Treatment: Xiongdan Wan
Phase: 2
Study Start date:
December 28, 2021
Estimated Completion Date:
August 30, 2022

Connect with a study center

  • Shanghai Mental Health Center

    Shanghai, Shanghai 200030
    China

    Site Not Available

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