NCT07334418
Early General Anesthesia to Limit Experiences of Trauma During Cesarean Section-Pilot Study
Recruiting
NAAges 18+InterventionalUniversity of PennsylvaniaInvestigator-initiated
~600 participants
Updated 2026-06-11 on ClinicalTrials.gov
What's tested:General anestheticIntravenous anesthetic
At a glance
Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Consent
Measured over From hospital admission through day of delivery
Conditions
Where it's being run
1 sites across 1 statesPennsylvania1
Who to contact
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Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
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
We will exclude patients who require induction of general anesthesia prior to umbilical cord clamping and by clinician determination.
What this trial measures
- ConsentFrom hospital admission through day of delivery
Study consent rate, defined as the number of patients consenting to participation among those approached for enrollment.