The Society for Obstetric Anesthesia and Perinatology Research Network General Anesthesia Registry

Description

The SOAP registry is a prospective, multicenter, electronic registry. The goal is to investigate the indications, mode of airway management, predisposing factors, and obstetric and anesthetic outcomes of pregnant patients who receive general anesthesia for cesarean delivery.

Conditions

Cesarean Delivery, General Anesthesia

Study Overview

Study Details

Study overview

The SOAP registry is a prospective, multicenter, electronic registry. The goal is to investigate the indications, mode of airway management, predisposing factors, and obstetric and anesthetic outcomes of pregnant patients who receive general anesthesia for cesarean delivery.

The Society for Obstetric Anesthesia and Perinatology Research Network General Anesthesia Registry

The Society for Obstetric Anesthesia and Perinatology Research Network General Anesthesia Registry

Condition
Cesarean Delivery
Intervention / Treatment

-

Contacts and Locations

Little Rock

University of Arkansas, Little Rock, Arkansas, United States, 72205

San Francisco

University of California San Francisco, San Francisco, California, United States, 94158

Stanford

Stanford University, Stanford, California, United States, 94303

Arvada

University of Colorado Hospital, Arvada, Colorado, United States, 80007

New Haven

Yale University, New Haven, Connecticut, United States, 06510

Gainesville

University of Florida, Gainesville, Florida, United States, 32610

Boise

St Lukes Anesthesia Associates of Boise, Boise, Idaho, United States, 83712

Chicago

University of Chicago Medical Center, Chicago, Illinois, United States, 60637

Indianapolis

Indiana University, Indianapolis, Indiana, United States, 46202

Iowa City

University of Iowa, Iowa City, Iowa, United States, 52242

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

    Ages Eligible for Study

    15 Years to 55 Years

    Sexes Eligible for Study

    FEMALE

    Accepts Healthy Volunteers

    Yes

    Collaborators and Investigators

    Yale University,

    Lisa Leffert, MD, PRINCIPAL_INVESTIGATOR, Yale Univesrity

    Study Record Dates

    2029-09