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Search / Trial NCT06030063

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

Launched by YALE UNIVERSITY · Aug 30, 2023

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

The Society for Obstetric Anesthesia and Perinatology (SOAP) is conducting a research study to learn more about the use of general anesthesia during cesarean deliveries. This study is collecting information from various hospitals to better understand why some pregnant women need general anesthesia, how their airways are managed during the procedure, and what outcomes they experience afterward. This information will help improve care for future patients.

To participate in this study, women must be between the ages of 15 and 55 and have received general anesthesia for a cesarean delivery. If eligible, participants can expect to share their experiences and medical details, which will be kept confidential. This study is currently recruiting participants, and it aims to gather valuable insights that could enhance the safety and effectiveness of anesthesia in cesarean deliveries.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • -Pregnant women aged 15-55 who have had a general anesthetic for Cesarean delivery

About Yale University

Yale University, a prestigious Ivy League institution located in New Haven, Connecticut, is renowned for its commitment to advancing medical research and clinical innovation. With a rich history of academic excellence and a robust infrastructure for scientific inquiry, Yale serves as a leading sponsor for clinical trials aimed at improving patient care and developing new therapeutic approaches. The university's multidisciplinary teams of researchers and clinicians collaborate to conduct rigorous and ethical studies, leveraging cutting-edge technologies and methodologies to address critical health challenges. Through its dedication to fostering an environment of inquiry and discovery, Yale University plays a pivotal role in translating research findings into clinical practice, ultimately enhancing health outcomes for diverse populations.

Locations

Rochester, Minnesota, United States

New Haven, Connecticut, United States

Durham, North Carolina, United States

Boston, Massachusetts, United States

Charleston, South Carolina, United States

Iowa City, Iowa, United States

Boston, Massachusetts, United States

Stanford, California, United States

Boston, Massachusetts, United States

Lebanon, New Hampshire, United States

Pittsburgh, Pennsylvania, United States

San Francisco, California, United States

Indianapolis, Indiana, United States

Nashville, Tennessee, United States

Little Rock, Arkansas, United States

Albuquerque, New Mexico, United States

Houston, Texas, United States

Gainesville, Florida, United States

Chicago, Illinois, United States

Albany, New York, United States

Baltimore, Maryland, United States

New York, New York, United States

New Haven, Connecticut, United States

Charlottesville, Virginia, United States

Manhasset, New York, United States

San Francisco, California, United States

Saint Louis, Missouri, United States

Temple, Texas, United States

Kansas City, Kansas, United States

Charleston, South Carolina, United States

Stanford, California, United States

Portland, Oregon, United States

Winston Salem, North Carolina, United States

Arvada, Colorado, United States

Stony Brook, New York, United States

Cincinnati, Ohio, United States

New Westminster, , Canada

Boise, Idaho, United States

Columbus, Ohio, United States

Patients applied

0 patients applied

Trial Officials

Lisa Leffert, MD

Principal Investigator

Yale Univesrity

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported