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Association of selenium with postpartum depression: a prospective observational study

Association of selenium with postpartum depression: a prospective observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400094098
Enrollment
Unknown
Registered
2024-12-17
Start date
2024-12-18
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

postpartum depression

Interventions

Observation group:None

Sponsors

The First Affiliated Hospital of Chongqing Medical University, Chongqing
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Age 20-40 years old; ASA grade II or III; Planned elective cesarean section; Pregnant women with no serious fetal malformations or defects during prenatal screening; The pregnant woman and her family members gave informed consent and signed for this experiment.

Exclusion criteria

Exclusion criteria: Prenatal mental illness; Maternal complications with other types of obstetric conditions, including severe preeclampsia, severe placenta previa, and placental abruption; Contraindications of intraspinal anesthesia.

Design outcomes

Primary

MeasureTime frame
Incidence of postpartum depression six weeks after operation;

Secondary

MeasureTime frame
Edinburgh Postpartum Depression scale score ;Postoperative exercise and resting pain NRS score;Selenium levels in plasma and cerebrospinal fluid ;Incidence of postpartum anxiety ;

Countries

China

Contacts

Public ContactLi Ping

The First Affiliated Hospital of Chongqing Medical University

8191170@qq.com+86 130 6233 7738

Outcome results

None listed

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