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Application of continuous noninvasive blood pressure monitoring in cesarean section of severe preeclampsia

Application of continuous noninvasive blood pressure monitoring in cesarean section of severe preeclampsia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089166
Enrollment
Unknown
Registered
2024-09-03
Start date
2024-10-01
Completion date
Unknown
Last updated
2024-09-09

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

Conditions

preeclampsia

Interventions

NICAP group:Non-Invasive Continuous Arterial Pressure monitoring
NIAP group:Non-invasive arterial pressure monitoring

Sponsors

Maternal and Child Health Hospital of Jinan City
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: ? Pregnant women who planned to undergo cesarean section were ASA anesthesia class II; ? Single term; ? Age 20-40 years old; ? Pregnancy age =37 weeks and =42 weeks; ?BMI 18.5-39.9; ? Participants in this study were voluntary and signed informed consent.

Exclusion criteria

Exclusion criteria: ?Parturient women with severe arrhythmia; ? Vascular diseases of upper limbs (recent vascular surgery, Raynaud's disease, vascular stenosis); ? The sensor cannot detect the pulse wave; ? Contraindications to spinal anesthesia; ? Placenta previa, fetal distress, developmental abnormalities; ? Parturient women allergic to the studied drugs.

Design outcomes

Primary

MeasureTime frame
hemodynamically stable time;

Secondary

MeasureTime frame
hypotension;

Countries

China

Contacts

Public ContactDongdong Qu

Maternal and Child Health Hospital of Jinan City

1272620722@qq.com+86 156 2455 0577

Outcome results

None listed

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