RecruitingNot ApplicableNCT07334418

Early General Anesthesia to Limit Experiences of Trauma During Cesarean Section-Pilot Study

EAGLET-CS Pilot: Early General Anesthesia to Limit Experiences of Trauma During Cesarean Section-Pilot Study


Sponsor

University of Pennsylvania

Enrollment

600 participants

Start Date

Apr 6, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Some patients who undergo cesarean section under spinal or epidural anesthesia can experience severe pain. Some patients who experience this kind of pain can experience symptoms of post-traumatic stress disorder (PTSD) after pregnancy. Currently, the two main options for treating this pain are general anesthesia (full medically induced unconsciousness) and using intravenous medications to reduce the pain and decrease anxiety. The EAGLET-CS Pilot is a pilot randomized trial that will test the feasibility of comparing the impact of these two options for preventing PTSD in a rigorous way for those patients who experience pain during their cesarean section after the baby is out.


Eligibility

Sex: FEMALEMin Age: 18 Years

Inclusion Criteria1

  • Women aged 18 or older undergoing non-emergent cesarean delivery with primary neuraxial (epidural, spinal, or CSE) anesthesia. Eligible patients will be those who report severe pain during surgery, defined as pain that does not resolve with 2 trials of first-line pharmacologic therapies (e.g., epidural supplementation with local anesthetics; intravenous opioid analgesics).

Exclusion Criteria1

  • We will exclude patients who require induction of general anesthesia prior to umbilical cord clamping and by clinician determination.

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Interventions

OTHERGeneral anesthetic

standard of care general anesthesia

OTHERIntravenous anesthetic

standard of care intravenous anesthesia


Locations(1)

Hospital of the University of Pennsylvania

Philadelphia, Pennsylvania, United States

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NCT07334418


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