Status:
ENROLLING_BY_INVITATION
Evaluation of the Typical Spinal Block During Cesarean Delivery
Lead Sponsor:
Oregon Health and Science University
Conditions:
Cesarean Section
Anesthesia, Obstetric
Eligibility:
FEMALE
15-55 years
Brief Summary
This will be a prospective, observational, single-center study to evaluate the accuracy of sensory testing by blunt 16-gauge plastic cannula during the 15 minutes after spinal injection for predicting...
Detailed Description
Primary Objective: 1\. Evaluate the accuracy of sensory testing with blunt plastic 16-gauge cannula during the 15 minutes after spinal injection for predicting spinal failure. Cephalad sensory dermat...
Eligibility Criteria
Inclusion
- Patients undergoing cesarean delivery under spinal or combined spinal epidural anesthesia
- BMI between 20 and 40 kg/m2
- Height between 5 feet 2 inches and 5 feet 10 inches.
- English and non-English speaking patients, if interpretive services are available
Exclusion
- Patient refusal
- Contraindications to neuraxial anesthesia (coagulopathy, CNS pathology, infection at site of needle puncture)
- Allergy to any study medications
- Use of epidural anesthesia
- Emergency (red) cesarean delivery
- Conditions that impact dermatomal sensory testing including spinal cord injury with sensory deficits and abdominoplasty
- Prison inmates
- Decisionally impaired individuals
- Pregnancies involving multiple fetuses
Key Trial Info
Start Date :
June 10 2024
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
January 31 2026
Estimated Enrollment :
250 Patients enrolled
Trial Details
Trial ID
NCT06206044
Start Date
June 10 2024
End Date
January 31 2026
Last Update
November 20 2024
Active Locations (1)
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1
Oregon Health and Science University
Portland, Oregon, United States, 97239