Spinal Aesthesia in Women With Placenta Previa Percreta

Completed

• Conditions: Complications; Cesarean Section
• Interventions: Procedure: spinal anesthesia; Procedure: general anesthesia

• Registration Number: NCT02686242
• Lead Sponsor: Air Force Military Medical University, China

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2015-12
• Study First Submitted: 2016-01-13
• Study First Submitted QC: 2016-02-18
• Study First Posted: 2016-02-19
• Primary Completion: 2016-03
• Study Completion: 2016-03
• Status Verified: 2016-06
• Last Update Submitted: 2016-06-21
• Last Update Posted: 2016-06-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 68

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
spinal anesthesia	spinal anesthesia	patients receive spinal anesthesia before general anesthesia
general anesthesia	general anesthesia	patients receive general anesthesia

Primary Outcome Measures

Name	Time	Method
incidence of hypotension	from beginning of the surgery to the end of the surgery,approximately 1 hour

Secondary Outcome Measures

Name	Time	Method
usage of norepinephrine	from beginning of the surgery to the end of the surgery,approximately 1 hour
dose of norepinephrine	from beginning of the surgery to the end of the surgery,approximately 1 hour
lowest systemic blood pressure	from beginning of the surgery to the end of the surgery,approximately 1 hour
maximal decrease of systemic blood pressure	from beginning of the surgery to the end of the surgery,approximately 1 hour

Trial Locations

Locations (1)

Xijing Hospital, Fourth Military Medical University; 🇨🇳 Xi'an, Shaanxi, China