Skip to content

Spinal Aesthesia in Women With Placenta Previa Percreta

Influence of Spinal Anaesthesia on Hemodynamic Stability in Women With Placenta Previa Percreta Undergoing Caesarean Section

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02686242
Acronym
SAW
Enrollment
68
Registered
2016-02-19
Start date
2015-12-31
Completion date
2016-03-31
Last updated
2016-06-22

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

Conditions

Complications; Cesarean Section

Keywords

cesarean section, spinal anesthesia, general anesthesia

Brief summary

Placenta previa percreta is a dangerous complication during surgery. Due to the high risk of hemorrhage, most parturients with placenta previa have to accept cesarean section. In this study investigators compare the effect of different anesthetic techniques on these patients.

Interventions

PROCEDUREspinal anesthesia

bupivacaine injected by spinal puncture

PROCEDUREgeneral anesthesia

general anesthesia with intubation

Sponsors

Air Force Military Medical University, China
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* women with placenta previa and increta-percreta (diagnosed by ultrasound and/or magnetic resonance imaging and confirmed during cesarean section) * women accepted cesarean section

Exclusion criteria

* women with baseline systemic blood pressure higher than 180 mmHg * women with coagulation disorder

Design outcomes

Primary

MeasureTime frame
incidence of hypotensionfrom beginning of the surgery to the end of the surgery,approximately 1 hour

Secondary

MeasureTime frame
usage of norepinephrinefrom beginning of the surgery to the end of the surgery,approximately 1 hour
dose of norepinephrinefrom beginning of the surgery to the end of the surgery,approximately 1 hour
lowest systemic blood pressurefrom beginning of the surgery to the end of the surgery,approximately 1 hour
maximal decrease of systemic blood pressurefrom beginning of the surgery to the end of the surgery,approximately 1 hour

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026