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OpenTrials
Completed

NCT Number: NCT02686242

Spinal Aesthesia in Women With Placenta Previa Percreta

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.

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Key information

Age range

18 year–65 year

Sex eligibility

Female

Study type

Observational

Primary location

Xijing Hospital, Fourth Military Medical University

Xi'an, Shaanxi, 710032, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Spinal anesthesia

Procedure

bupivacaine injected by spinal puncture

General Anesthesia

Procedure

general anesthesia with intubation

Primary outcomes

  1. incidence of hypotension

    Time frame: from beginning of the surgery to the end of the surgery,approximately 1 hour

Secondary outcomes

  1. usage of norepinephrine

    Time frame: from beginning of the surgery to the end of the surgery,approximately 1 hour

  2. dose of norepinephrine

    Time frame: from beginning of the surgery to the end of the surgery,approximately 1 hour

  3. lowest systemic blood pressure

    Time frame: from beginning of the surgery to the end of the surgery,approximately 1 hour

  4. maximal decrease of systemic blood pressure

    Time frame: from beginning of the surgery to the end of the surgery,approximately 1 hour

Sponsors and collaborators

Lead sponsor

Air Force Military Medical University, China

Other

Registry information

Official study title

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

Acronym: SAW

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Feb 19, 2016
Registry last updated
Jun 22, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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