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Implementation of continuous noninvasive hemodynamic monitoring during cesarean section

Implementation of continuous noninvasive hemodynamic monitoring during cesarean section

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900025246
Enrollment
Unknown
Registered
2019-08-17
Start date
2019-09-01
Completion date
Unknown
Last updated
2019-08-27

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

Conditions

Obstetrics Anesthesia

Interventions

experimental group:continuous noninvasive hemodynamic monitoring

Sponsors

Sheng Jing Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1)aged 22 to 35; 2) single birth; 3) full term, which is defined as defined as gestation 37~41 weeks.

Exclusion criteria

Exclusion criteria: The exclusion consisted of undergoing general anesthesia or upper level of blockade exceeding T6, known fetal abnormalities, and being allergic to related agents.

Design outcomes

Primary

MeasureTime frame
hymodynamic parameters;—

Countries

China

Contacts

Public ContactPing Zhao

Shengjing Hospital of China Medical University

sn1418@163.com+86 1894025897

Outcome results

None listed

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