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Intraoperative monitoring of stroke volume variation versus central venous pressure in pregnant women with placenta accreta.

Intraoperative monitoring of stroke volume variation in cesarean section.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800020356
Enrollment
Unknown
Registered
2018-12-25
Start date
2019-01-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

placenta accreta

Interventions

Group 1:Goal directed fluid management based on central venous pressure
Group 2:Goal directed fluid management based on central venous pressure
Group 3:Goal directed fluid management based on stroke volume variation

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 49 Years

Inclusion criteria

Inclusion criteria: 1. pregnant women aged 18-49 years old; 2. ASA I-III; 3. weeks of gestation =28 weeks; 4. planned cesarean section to terminate the pregnancy; 5. placenta accreta.

Exclusion criteria

Exclusion criteria: 1. severe aortic regurgitation; 2. severe arrhythmia; 3. left ventricular ejection fraction (LVEF)<40%; 4. patients who refused to participation; 5. emergency cases.

Design outcomes

Primary

MeasureTime frame
central venous pressure;stroke volume variation;blood pressure;heart rate;blood blos;the amount of blood transfusion;hourly urine volume;the amount of fluid transfusion;—

Secondary

MeasureTime frame
blood gas analysis;blood routine analysis;blood coagulation system;liver and renal function;application of norepinephrine;postoperative complications;length of hospital stay;—

Countries

China

Contacts

Public ContactLi Liang

Qilu Hospital of Shandong University

liliang6785@126.com+86 15966627716

Outcome results

None listed

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