RecruitingPhase 4NCT05826327

Effects of Epidural Labor Analgesia With Esketamine on the Incidence of Postpartum Depression in Parturients

Effects of Epidural Labor Analgesia With Esketamine on the Incidence of Postpartum Depression and Maternal and Neonatal Outcomes in Parturients With Prenatal Depression


Sponsor

Women's Hospital School Of Medicine Zhejiang University

Enrollment

364 participants

Start Date

May 1, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

Postpartum depression is a common psychological abnormality during the puerperium, which seriously affects maternal and neonatal health. Esketamine, the S-enantiomer of ketamine, is twice as potent as ketamine and can be safely used for cesarean section and labor analgesia. However, it is not clear whether esketamine used for epidural labor analgesia can significantly reduce the incidence of postpartum depression. This study intends to explore the incidence of maternal prenatal depression and to investigate the effect of esketamine for epidural labor analgesia on postpartum depression and maternal and neonatal outcomes in parturients with prenatal depression through a multi-center, large-scale and high-quality clinical trail, in order to provide a clinical basis and theoretical basis for the application of esketamine used for epidural labor analgesia in postpartum depression and further reduce the incidence of postpartum depression, promote maternal and infant health, and ensure maternal and infant safety .


Eligibility

Sex: FEMALEMin Age: 18 Years

Inclusion Criteria1

  • Full-term pregnancy; Antenatal depressive state (EPDS score ≥10 and non-depressive diagnosis by a psychiatrist); Epidural labor analgesia; Signed informed consent.

Exclusion Criteria1

  • Pre-existing history of definite psychiatric disorders (depression, schizophrenia, etc.) or communication disorders;Presence of severe preoperative pregnancy complications (e.g., severe preeclampsia, placental implantation, HELLP syndrome, placenta praevia, placenta abruptio);ASA classification ≥ grade III;Contraindications to ketamine/S-ketamine (e.g., intractable, refractory hypertension, severe cardiovascular disease \[cardiac function class ≥ III\], hyperthyroidism); Refusal to participate in the study.

Interventions

DRUGEsketamine

The drug esketamine will be added to the experimental group as opposed to the control group.

DRUGSufentanil

Sufentanil for labour analgesia in the control group


Locations(1)

Women's hospital, school of medicine, Zhejiang university

Hangzhou, Zhejiang, China

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NCT05826327


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