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Construction and clinical application verification of venlafaxine antidepressant efficacy prediction model based on multi-omics integration analysis

Construction and clinical application verification of venlafaxine antidepressant efficacy prediction model based on multi-omics integration analysis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500111766
Enrollment
Unknown
Registered
2025-11-05
Start date
2025-11-07
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

Depression

Interventions

Venlafaxine treatment group:NA

Sponsors

Affiliated Kangning Hospital of Ningbo University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with depression through DSM-5, aged 18-65 years old; 2. Baseline HAMD-17 score of 7 or above; 3. First occurrence or recurrence without medication use (> 3 months); 4. No significant risk of suicide (score of the suicide item in the Hamilton Depression Rating Scale is less than 3 points).

Exclusion criteria

Exclusion criteria: 1. Patients with mental disorders such as bipolar disorder and schizophrenia; 2. Patients with refractory depression (those who have failed to respond to >= 2 types of adequate antidepressant treatments in the past); 3. Patients with severe physical illnesses; 4. Substance abusers.

Design outcomes

Primary

MeasureTime frame
HAMD-17-item scale score;Pharmacogenomics;proteomics;metabolomics;

Secondary

MeasureTime frame
Venlafaxine concentration;

Countries

China

Contacts

Public ContactTian Haihua

Affiliated Kangning Hospital of Ningbo University

13857478208@163.com+86 574 26302554

Outcome results

None listed

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