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Clinical effect of low-dose esketamine in assisting combined spinal-epidural anesthesia for cesarean section

Clinical effect of low-dose esketamine in assisting combined spinal-epidural anesthesia for cesarean section

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040375
Enrollment
Unknown
Registered
2020-11-28
Start date
2020-12-01
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

Obstetric Anesthesia

Interventions

Case series:Intravenous esketamine 0.15mg/kg

Sponsors

Dept. of Anesthesiology International Peace Maternity & Child Health Hospital, Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
22 Years to 40 Years

Inclusion criteria

Inclusion criteria: Women aged 22-40 years, single birth, head position, term, ASA grade II, and undergoing elective cesarean section

Exclusion criteria

Exclusion criteria: There are absolute and relative contraindications in combined spinal-epidural anesthesia; allergies to local anesthetics; severe cardiopulmonary; preoperatively found fetal distress; fetal malformation or polypeptide pregnancy

Design outcomes

Primary

MeasureTime frame
Maternal Intraoperative Situation;—

Secondary

MeasureTime frame
Neonatal outcome;Maternal postoperative outcome;—

Countries

China

Contacts

Public ContactXu Tao

International Peace Maternity & Child Health Hospital, Shanghai Jiaotong University School of Medicine

towerxutao@163.com+86 18918098660

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 20, 2026