Geneva, Feb. 13 -- International Clinical Trials Registry received information related to the study (ChiCTR2600118349) titled 'The application value of heart rate variability parameters in the ICU sedation and analgesia after cesarean section in patients with severe preeclampsia' on Feb. 4.
Study Type: Interventional study
Study Design:
Parallel
Primary Sponsor: Shijiazhuang Maternity Hospital/Shijiazhuang Fourth Hospital
Condition:
Severe preeclampsia
Intervention:
Trial group:HRV monitoring + routine sedation and analgesia
Recruitment Status: Not Recruiting
Phase: N/A
Date of First Enrollment: 2026-02-10
Target Sample Size: Trial group:48;Control group:48;
Countries of Recruitment:
China
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