CompletedNot Applicable

Rivanna Ultrasound for Neuraxial Block

United States128 participantsStarted 2017-10-23

Plain-language summary

We hypothesize that the Rivanna Accuro or similar U/S device would reduce time to success of identifying epidural and/or intrathecal spaces as compared to conventional palpation method.

Who can participate

Age range18 Years – 50 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * BMI \>30 * Female requesting analgesia for delivery, be it via vaginal or cesarean delivery Exclusion Criteria: * Allergy to ultrasound gel * Contraindication to receiving neuraxial analgesia * Under the age of 18

What they're measuring

Time to Success of Neuraxial Block Placement

Timeframe: 60-225 seconds

Trial details

NCT IDNCT03214640

SponsorWake Forest University Health Sciences

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-04-13

Results submitted2021-03-26

View on ClinicalTrials.gov More Analgesia trials