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The application of LiDCOrapid system in observation of hemodynamic changes in severe preeclampsia patients during cesarean delivery under spinal anesthesia

The application of LiDCOrapid system in observation of hemodynamic changes in severe preeclampsia patients during cesarean delivery under spinal anesthesia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800016378
Enrollment
Unknown
Registered
2018-05-28
Start date
2018-06-01
Completion date
Unknown
Last updated
2018-06-05

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

Conditions

severe preeclampsia patients

Interventions

Case series:spinal anesthesia

Sponsors

the Chifeng Municipal Hospital, Hongshan District, Chifeng City, Inner Mongolia
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. preeclampsia was regarded as severe according to "obstetrics and Gynecology" Eighth Edition; 2. the 28 to 40 weeks of pregnancy; 3. the body weight index 28-35 kg/m2; 4. the single pregnancy; 5. the subjects were enrolled in this study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. any contraindication to SA; 2. any contraindication to radial artery puncture; 3. patient refusal; 4. chronic hypertension, placental abruption, placenta previa, coagulation abnormality etc; 5. Should any spinal anesthetic take longer than 30 min to perform, the patient would receive general anesthesia and be withdrawn from the study.

Design outcomes

Primary

MeasureTime frame
cardiac output;—

Countries

China

Contacts

Public ContactLiu Chaoqun

the Chifeng Municipal Hospital, Hongshan District, Chifeng City, Inner Mongolia

1060204797@qq.com+86 13722148630

Outcome results

None listed

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