The Society for Obstetric Anesthesia and Perinatology Research Network General Anesthesia Registry (NCT06030063)
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: University of Arkansas — Little Rock, Arkansas
Age range: 15 Years to 55 Years
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (35 Sites)
Showing the first 25 of 35 sites.
- University of Arkansas — Little Rock, Arkansas
- University of California San Francisco — San Francisco, California
- Stanford University — Stanford, California
- University of Colorado Hospital — Arvada, Colorado
- Yale University — New Haven, Connecticut
- University of Florida — Gainesville, Florida
- St Lukes Anesthesia Associates of Boise — Boise, Idaho
- University of Chicago Medical Center — Chicago, Illinois
- Indiana University — Indianapolis, Indiana
- University of Iowa — Iowa City, Iowa
- University of Kansas Health System — Kansas City, Kansas
- University of Maryland School of Medicine — Baltimore, Maryland
- Brigham & Women's Hospital — Boston, Massachusetts
- Boston Medical Center — Boston, Massachusetts
- Beth Israel Deaconess Medical Center — Boston, Massachusetts
- Mayo Clinic — Rochester, Minnesota
- Mercy Hospital St. Louis — St Louis, Missouri
- Dartmouth-Hitchcock Medical Center — Lebanon, New Hampshire
- University of New Mexico — Albuquerque, New Mexico
- Albany Medical Center — Albany, New York
- Northwell Health — Manhasset, New York
- Icahn School of Medicine at Mount Sinai — New York, New York
- Renaissance School of Medicine Stony Brook University — Stony Brook, New York
- Duke University Medical Center — Durham, North Carolina
- Atrium Health Wake Forest Baptist Medical Center — Winston-Salem, North Carolina
📞 Contact the Study Coordinator
Phone: (203) 785-4304
Email: lisa.leffert@yale.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Cesarean Delivery
- IC-CS Risk: Patient Outcomes — Ann Arbor, Michigan
- Adding Dexmedetomidine or Clonidine to Spinal Anesthesia for Cesarean Delivery — New York, New York
- BUprenorphine Versus Morphine for Postcesarean Analgesia (BUMP) — New York, New York
- Duration of Urinary Catheterization Following Cesarean Deliveries Under Neuraxial Anesthesia — Vancouver, British Columbia
- Suzetrigine for Opioid-Free Recovery After Cesarean Delivery — Austin, Texas
- Post-cesarean Analgesia: Comparing Effectiveness of Staggered v. Simultaneous Therapies — Philadelphia, Pennsylvania
Explore by condition: All Cesarean Delivery clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.