A Multicenter Clinical Study on Shuganjieyu Capsule Combined With Fluoxetine in the Treatment of Depression

NCT ID: NCT05361330

Last Updated: 2022-05-17

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 160 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-05-30
• Study Completion Date: 2023-09-30

Brief Summary

This study mainly evaluates the efficacy and safety of Shuganjieyu capsule combined with Fluoxetine as well as the Fluoxetine monotherapy for the treatment of depression in the basic study, and also explores the efficacy for the extended study period as well as the efficacy and safety for the full trial period (basic study period and extended study period).

Detailed Description

Whole-course treatment serves as the principle for the treatment of depression, including symptom control in the acute phase, relapse prevention in the consolidation period and recurrence prevention in the maintenance period. Western medicine usually adopts antidepressant drugs combined with psychotherapy, mainly antidepressant SSRI at the current stage. It can selectively inhibit serotonin reuptake, so as to play an antidepressant role, but for somatic symptoms, the effect is general. Based on the overall regulation of body and mind, traditional Chinese medicine aims to achieve individualized treatment combing syndrome differentiation and treatment in a multi-channel, multi-target, and multi-level manner. At present, the combined application of antidepressant chemical drugs and Chinese patent medicines is complementary to each other from the perspective of mechanism and clinical practice. However, the study of Shuganjieyu capsule combined with antidepressant chemical drugs is mostly concentrated in the short term, and the benefits of long-term combined use of Shuganjieyu capsule remain to be further studied.

The purpose of this multicenter clinical study is to evaluate the efficacy and safety of Shuganjieyu capsule combined with Fluoxetine as well as the Fluoxetine monotherapy in the basic study period. Besides, the study aims to continue to observe the efficacy and safety in the extended study research period, so as to provide important clinical data for the whole-course medication.

Recruitment of outpatients / inpatients with depression. After screening the patients who met the inclusion criteria, the study collected demographic data, recorded symptoms and scale scores and improved relevant laboratory tests. The experimental group was treated with Shuganjieyu capsule combined with Fluoxetine, and the control group was treated with Fluoxetine. The related indexes were evaluated 2 ,4, 8, 12, 16 and 24 weeks later.

Conditions

Outpatients / Inpatients With Depression

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

The experimental group: Shuganjieyu capsule

Shuganjieyu capsule combined with Fluoxetine

Group Type: EXPERIMENTAL

Shuganjieyu capsule

Intervention Type: DRUG

2 capsules each time, twice per day. According to the study progress, the intervention can be adjusted to 4 capsules each time, twice per day

Fluoxetine

Intervention Type: DRUG

Medication in basic study period: Fluoxetine (20 mg, once a day) Medication in the expanded study period: After 8 weeks of basic study period, if the reduction rate of HAMD-17 total scores is below 50 %, for the treatment group, the dosage of Fluoxetine will be adjusted to 40 mg / time, once a day.

The control group: Shuganjieyu capsule simulator

Fluoxetine monotherapy

Group Type: PLACEBO_COMPARATOR

Fluoxetine

Intervention Type: DRUG

Medication in basic study period: Fluoxetine (20 mg, once a day) Medication in the expanded study period: After 8 weeks of basic study period, if the reduction rate of HAMD-17 total scores is below 50 %, for the treatment group, the dosage of Fluoxetine will be adjusted to 40 mg / time, once a day.

Interventions

Shuganjieyu capsule

2 capsules each time, twice per day. According to the study progress, the intervention can be adjusted to 4 capsules each time, twice per day

Intervention Type: DRUG

Fluoxetine

Medication in basic study period: Fluoxetine (20 mg, once a day) Medication in the expanded study period: After 8 weeks of basic study period, if the reduction rate of HAMD-17 total scores is below 50 %, for the treatment group, the dosage of Fluoxetine will be adjusted to 40 mg / time, once a day.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. In line with the diagnostic criteria for depression of Diagnostic and Statistical Manual of Mental Disorders (5th edition) (DSM-5);

2. Age: 18-65 (including 18 and 65), gender unlimited;

3. Hamilton Rating Scale for Depression (HAMD-17) score≥18 in the screening period, and the 13th score≥2;

4. For women of childbearing age, pregnancy test must be negative and not in lactation. The contraception measure must be accepted by the Investigators. Participants should agree to maintain this measure throughout the whole process;

5. Sign the informed consent form voluntarily and agree to participate in all visits, examinations and treatment as required by the trial protocol.

Exclusion Criteria

1. Treatment-resistant depression (patients with poor clinical efficacy of antidepressants with two or more different mechanisms after sufficient and full course of treatment);

2. Patients who meet DSM-5 diagnostic criteria for other mental disorders (such as schizophrenia pedigree and other mental disorders, bipolar and related disorders, anxiety disorders, obsessive-compulsive and related disorders, somatic symptoms and related disorders);

3. Depression caused by psychoactive drugs;

4. Patients with severe suicide (HAMD-17 suicide score≥3) and injury tendency;

5. Patients with serious or unstable cardiovascular, cerebrovascular, liver, kidney, endocrine, digestive and blood diseases;

6. Depressive episodes secondary to other mental diseases or somatic diseases at an active stage;

7. ALT and AST values in the liver function examination are more than double the upper limit of reference value, or Scr value is above the upper limit of reference value;

8. Patients with a history of endocrine diseases such as hyperthyroidism and hypothyroidism who are currently active;

9. Patients who had undergone psychiatric surgery or electroconvulsive therapy in the past three months;

10. Anyone with an allergic constitution known or suspected to have an allergic history to Hypericum perforatum L., Eleutherococcus senticosus and Fluoxetine;

11. Those who have previously failed Shuganjieyu capsule or Fluoxetine treatment;

12. Women in pregnancy or lactation period. Women who plan to get pregnant during the study and within six months;

13. Patients with psychoactive substance abuse or dependence in the past 12 months;

14. Long-term use of caffeine and nicotine;

15. Patients who have received or are receiving any other clinical trial drug treatment within three months before the trial;

16. Patients who are taking drugs that interfere with the efficacy evaluation of the investigational drugs, and drugs that are forbidden to be used in combination with the test drugs. Patients who have received antidepressant drugs for systematical treatment within 4 weeks;

17. Those who are regarded as unsuitable by investigators for this clinical trial.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Sichuan Jishengtang Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role: collaborator

Peking University

OTHER

Sponsor Role: lead

Responsible Party

Si Tianmei

Vice President of Institute of Mental Health, Peking University Sixth Hospital, Director of Research Laboratory on Psychopharmacology of Institute of Mental Health, Peking University Sixth Hospital

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Nanjing Brain Hospital, Nanjing Medical University

Nanjing, Jiangsu, China

First Hospital, Shanxi Medical University

Taiyuan, Shanxi, China

Institute of Mental Health, Peking University Sixth Hospital

Beijing, , China

Countries

China

Central Contacts

Tianmei Si, PhD., MD.

Role: CONTACT

sitianmei@bjmu.edu.cn

861062723748

Facility Contacts

Zhijian Yao, MD.

Role: primary

zjyao@njmu.edu.cn

86-025-82296670

Zhifen Liu, MD.

Role: primary

liuzhifen5518@163.com

86-13703586547

Tianmei Si, PhD., MD.

Role: primary

sitianmei@bjmu.edu.cn

861062723748

Other Identifiers

V2.0

Identifier Type: -

Identifier Source: org_study_id