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Maternal placental perfusion Changes After Crystalloid or Colloid Coload Following Spinal Anesthesia for Elective Cesarean Delivery

Maternal placental perfusion Changes After Crystalloid or Colloid Coload Following Spinal Anesthesia for Elective Cesarean Delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004116
Enrollment
Unknown
Registered
2014-01-05
Start date
2014-01-15
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

hypotention

Interventions

crystalloid Group:crystalloid coload
colloid Group:colloid coload

Sponsors

Department of Anesthesiology, Obstetrics and Genecology Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 60 ASA I and II women scheduled for elective cesarean delivery were recruited

Exclusion criteria

Exclusion criteria: Patients show no will to participate in the study or refuse to sign the informed consentchronic or pregnancy-induced hypertension, diabetes on medication, cardiovascular or cerebrovascular disease, fetal abnormalities, gestational age 100 kg) and height (180 cm) and any contraindications to neuraxial anesthesia.

Design outcomes

Primary

MeasureTime frame
systolic velocity : diastolic velocity;neonatal acid- base;—

Countries

China

Contacts

Public ContactHUANG Shao-qiang

Department of Anesthesiology, Obstetrics and Genecology Hospital, Fudan University

timrobbins71@163.com+86 13918210787

Outcome results

None listed

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