Clinical observation of epidural labor analgesia on postpartum depression in pregnant women

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2000038504

Enrollment

Unknown

Registered

2020-09-23

Start date

2020-10-01

Completion date

Unknown

Last updated

2020-11-30

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

Conditions

Postpartum depression

Interventions

Case series:No

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: First-borns prepared for vaginal delivery in the head position of a full-term single fetus; aged 18 to 35 years old; No history of depression in the past or during pregnancy, and no use of psychiatric drugs during pregnancy; Informed consent

Exclusion criteria

Exclusion criteria: The maternal; A history of depression or other mental illness; Oral antidepressants and other drugs during pregnancy; Contraindications for epidural labor analgesia; Gestational weeks <37 or 42 weeks; Twin or multiple births

Design outcomes

Primary

Measure	Time frame
EPDS score at 6 weeks postpartum;	—

Secondary

Measure	Time frame
Maternal satisfaction with labor analgesia;	—

Countries

China

Contacts

Public ContactTang Xianning

The First Affiliated Hospital of Chongqing Medical University

865094219@qq.com19942331062

Outcome results

None listed

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