Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu
Trial record 1 of 4 for:    "Placenta Praevia" | "Anesthetics"
Previous Study | Return to List | Next Study

Spinal Aesthesia in Women With Placenta Previa Percreta (SAW)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02686242
Recruitment Status : Completed
First Posted : February 19, 2016
Last Update Posted : June 22, 2016
Sponsor:
Information provided by (Responsible Party):
Zhihong LU, Fourth Military Medical University

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.

Condition or disease Intervention/treatment
Complications; Cesarean Section Procedure: spinal anesthesia Procedure: general anesthesia

Layout table for study information
Study Type : Observational
Actual Enrollment : 68 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Influence of Spinal Anaesthesia on Hemodynamic Stability in Women With Placenta Previa Percreta Undergoing Caesarean Section
Study Start Date : December 2015
Actual Primary Completion Date : March 2016
Actual Study Completion Date : March 2016

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Cesarean Section

Group/Cohort Intervention/treatment
spinal anesthesia
patients receive spinal anesthesia before general anesthesia
Procedure: spinal anesthesia
bupivacaine injected by spinal puncture

general anesthesia
patients receive general anesthesia
Procedure: general anesthesia
general anesthesia with intubation




Primary Outcome Measures :
  1. incidence of hypotension [ Time Frame: from beginning of the surgery to the end of the surgery,approximately 1 hour ]

Secondary Outcome Measures :
  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 ]


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
parturients with placenta praevia/accreta scheduled for cesarean section
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02686242


Locations
Layout table for location information
China, Shaanxi
Xijing Hospital, Fourth Military Medical University
Xi'an, Shaanxi, China, 710032
Sponsors and Collaborators
Fourth Military Medical University
Investigators
Layout table for investigator information
Study Chair: Hailong Dong Xijing hosptial

Publications:
Layout table for additonal information
Responsible Party: Zhihong LU, Dr., Fourth Military Medical University
ClinicalTrials.gov Identifier: NCT02686242     History of Changes
Other Study ID Numbers: XJH-A-2015-6-6-01
First Posted: February 19, 2016    Key Record Dates
Last Update Posted: June 22, 2016
Last Verified: June 2016
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided
Keywords provided by Zhihong LU, Fourth Military Medical University:
cesarean section
spinal anesthesia
general anesthesia
Additional relevant MeSH terms:
Layout table for MeSH terms
Placenta Previa
Obstetric Labor Complications
Pregnancy Complications
Placenta Diseases
Anesthetics
Central Nervous System Depressants
Physiological Effects of Drugs