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Evaluation of prenatal depression and screening study of specific markers

Evaluation of prenatal depression and screening study of specific markers

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112828
Enrollment
Unknown
Registered
2025-11-20
Start date
2025-11-26
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Antepartum depression

Interventions

Depression group:None
Non-depressed group:None

Sponsors

Nanjing Maternal and child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Pregnant women of childbearing age (18 to 45 years old) who are scheduled to undergo subarachnoid anesthesia (including combined epidural and subarachnoid anesthesia) for cesarean section and those who are scheduled to undergo cervical cerclage during pregnancy.

Exclusion criteria

Exclusion criteria: Exclusion criteria: Pregnant women who are scheduled to undergo other forms of anesthesia, those with gestational hypertension (preeclampsia), and other metabolic disorders, as well as patients with a clear diagnosis of mental disorders (such as schizophrenia, depression, anxiety disorder, paranoia, mania, post-traumatic stress disorder and obsessive-compulsive disorder).

Design outcomes

Primary

MeasureTime frame
Degree of perinatal depression;Differential markers of perinatal depression;

Secondary

MeasureTime frame
Postpartum maternal functional magnetic resonance imaging examination (routine cranial plain scan + 3D T1 + resting-state Bold + DTI);

Countries

China

Contacts

Public ContactMing Jiang

Nanjing Maternal and child Health Care Hospital

njfyjiangming@163.com+86 139 1296 1506

Outcome results

None listed

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