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To study the effect of probiotics adjuvant therapy on depressive symptoms in hospitalized patients with moderate to severe depression

To study the effect of probiotics adjuvant therapy on depressive symptoms in hospitalized patients with moderate to severe depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081287
Enrollment
Unknown
Registered
2024-02-28
Start date
2024-03-01
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Depression

Interventions

Intervention group:Prescribed probiotics were taken daily for eight weeks.
placebo:Placebo was administered daily for eight weeks

Sponsors

The Second People's Hospital of Lishui
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1)Age: >18 years; (2)Have received formal education =6 years; (3)Patients with moderate to severe depressive disorder were diagnosed according to the ICD-10 diagnostic criteria(F32.1F32.2F32.3F33.1F33.2F33.3), Hamilton Depression Scale > 17; (4)Newly hospitalized patients in the Second People's Hospital of Lishui(Time of admission < 2weeks); (5)Signed an informed consent form.

Exclusion criteria

Exclusion criteria: (1)Had psychotic symptoms such as hallucinations and delusions, and had serious suicidal tendencies; (2)History of alcohol and substance abuse; (3)Systemic use of antibiotics or antifungal agents within 30 days before the study; (4)History of severe food allergy, including cow's milk allergy; (5)Pregnant and lactating women; (6)Other serious medical conditions (uncontrolled diabetes, uncontrolled hypertension, hyperlipidemia, obesity BMI> 25, cardiovascular disease with antiplatelet or anticoagulant therapy, severe gastrointestinal diseases such as Crohn's disease and ulcerative colitis); (7)Use of probiotic products within six months; (8)Inability to comply with study requirements.

Design outcomes

Primary

MeasureTime frame
Symptoms of depression;

Secondary

MeasureTime frame
Self-reported psychological attributes;Biomarkers;

Countries

China

Contacts

Public ContactKe Zhao

The Second People's Hospital of Lishui

zhaoke@wmu.edu.cn+86 136 4587 9591

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026