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Clinical Study of Buzhong Yiqi Decoction on Qi-Deficiency Constitution and Its Impact on the Onset of Depression

Clinical Study of Buzhong Yiqi Decoction on Qi-Deficiency Constitution and Its Impact on the Onset of Depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000178
Enrollment
Unknown
Registered
2026-01-24
Start date
2026-01-26
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

depression

Interventions

Qi-deficiency constitution intervention group:Administer Buzhong Yiqi Tang Granules for 4 weeks, and follow up for 2 years
Qi-deficiency constitution control group:Placebo was given for 4 weeks, followed by a 2-year follow-up

Sponsors

Integrated Traditional Chinese and Western Medicine Hospital, Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 25 Years

Inclusion criteria

Inclusion criteria: 1. Healthy population; 2. Traditional Chinese medicine constitution evaluation conforms to the diagnostic criteria of individuals with simple qi deficiency constitution or those with peaceful constitution 3. Gender is not limited, age is 18-25 years old; 4. The subjects are informed and voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Women who are pregnant or breastfeeding. 2. History of surgery or severe trauma within the past 1 month. 3. Major medical or surgical diseases newly identified or suspected at the first health examination (e.g., cardiovascular, respiratory, digestive, urinary, hematologic, endocrine disorders), or being in an active phase of chronic disease, or with psychiatric/psychological disorders. 4. Functional gastrointestinal disorders or psychiatric/psychological disorders identified or suspected based on medical history inquiry and physical examination. 5. Long-term occupational exposure to hazardous substances. 6. Long-term night-shift work or reversed day–night circadian rhythm. 7. Currently participating in other clinical trials. 8. Any other condition deemed by the investigators to make the participant unsuitable for this study. 9. Severe unhealthy lifestyle habits. 10. Use of antibiotics or microecological modulators (e.g., probiotics/prebiotics or similar agents) within 2 months prior to sample collection.

Design outcomes

Primary

MeasureTime frame
Depression scale assessment;Assessment using a depression rating scale;

Secondary

MeasureTime frame
Health status score;

Countries

China

Contacts

Public ContactChen Jieyu

Integrated Traditional Chinese and Western Medicine Hospital, Southern Medical University

876072054@qq.com+86 135 7053 2831

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 7, 2026