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
Eligibility Criteria
Inclusion
Inclusion Criteria:
- 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.
- Outpatients.
- Male or female subjects aged 18-65 years.
- HAMD-17 score of the baseline period and screening period is 18-24.
- Women of childbearing potential must be willing to use acceptable methods ofcontraception throughout the study period and the following one month.
- The patient fully understands and signs the informed consent form.
Exclusion
Exclusion Criteria:
- Patient has survived a suicide attempt or has acute suicidal tendencies (HAMD-17 Item3 ≥3).
- Comorbidity according to DSM-IV-TR, axis-I except for major depressive disorder.
- HAMD-17 reduction ratio ≥25% within one week from the screening to the baselineperiod.
- Depressive episode secondary to psychiatric illness or somatic disease.
- Serious and unstable diseases such as cerebrovascular disease; liver and kidneydisease; disease of internal secretion (abnormal thyroid function); hemopathy;seizures, or other encephalopathies.
- History of alcohol or drug abuse over the last 6 months.
- Allergic history to Xiongdan Wan, or serious drug allergic history.
- Pregnant or lactating women and women of childbearing potential throughout the studyperiod; men who have the desire of fertility within six months.
- 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.
- Treatment with modified electroconvulsive therapy (MECT) or repetitive transcranialmagnetic stimulation (rTMS) in the past three months.
- 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
ChinaSite Not Available
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