Geneva, July 7 -- International Clinical Trials Registry received information related to the study (ChiCTR2600127062) titled 'Low-dose dexmedetomidine plus esketamine for improving sleep quality after cesarean section' on June 23.
Study Type: Interventional study
Study Design:
Parallel
Primary Sponsor: Hefei Maternal and Child Health Hospital
Condition:
postoperative sleep disturbance, postoperative pain, and postpartum depression.
Intervention:
Esketamine group:Intravenous esketamine injection alone after fetal delivery
Control group:Simple local anesthesia protocol
Recruitment Status: Not Recruiting
Phase: 4
Date of First Enrollment: 2026-07-01
Target Sample Size: Esketamine group:87;Control group:87;Dexmedetomidine combi...