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A study of blood lipid metabolism in patients with depressive disorder in adolescents

A study of blood lipid metabolism in patients with depressive disorder in adolescents

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400089218
Enrollment
Unknown
Registered
2024-09-04
Start date
2024-09-05
Completion date
Unknown
Last updated
2024-09-09

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

Conditions

Bipolar disorder

Interventions

Observation group(Bipolar disorder depressive episode. Drug intervention: Sertraline, quetiapine and combined with magnesium valproate were given in the case group, and blood lipid metabolomics level
control group (Venous blood was collected for lipid metabolomics.):None

Sponsors

Ningxia Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 29 Years

Inclusion criteria

Inclusion criteria: Case group:?All patients met the criteria for DSM-V diagnosis of depressive episodes with bipolar II disorder without psychotic symptoms (two or more attending doctors clearly diagnosed depressive disorders according to the criteria);? Between the ages of 18 and 29; ? The total score of the 17-item HAMD depression scale was =17 points;? Female subjects were required to consent to effective contraceptive use prior to enrollment and throughout the study. Fertile female subjects must have a negative urine pregnancy test at the time of screening; ? The informed consent is signed by the patient and/or legal guardian. Control group :? no diagnosis of mental illness;?Age: 18-29 years old; ? No history of major physical diseases and genetic history; ? Sign informed consent.

Exclusion criteria

Exclusion criteria: Case group:? Physical diseases, endocrine diseases, heart diseases, immune system related diseases, etc.; ?Acute and chronic infection within a month; ? Used drugs that affect lipid metabolism within 2 weeks; ? Those who have participated in strenuous exercise within 1 week; Alcohol or drug abusers; ? Taking antipsychotic drugs within 1 month before enrollment;;? 6 months before the group received electrical convulsions or brain stimulation treatment; ? Severe abnormal liver and kidney function;? People who are receiving hypoglycemic drugs, antihypertensive drugs, lipid-lowering drugs and drugs that affect uric acid levels; ? Severe cardiovascular disease;? Lactating or pregnant women; Diseases of the blood system. Control group :? serious physical disease or recently undergone surgery; ? Patients with organic brain diseases or dementia; ? Pregnant or lactating women; ? Drug abusers.

Design outcomes

Primary

MeasureTime frame
Changes of blood lipid metabolomics after 0, 3 and 8 weeks of medication;Hamilton depression scale;Hamilton Anxiety Scale;Young manic rating scale;Negative symptom scale;Negative symptom scale;Non-suicidal self-injury behavior;Drug efficacy;

Secondary

MeasureTime frame
Suicide risk;

Countries

China

Contacts

Public ContactChenYanhua

Mental Health Center, General Hospital of Ningxia Medical University

1052703852@qq.com+86 951 674 3760

Outcome results

None listed

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