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Search / Trial NCT06206044

Evaluation of the Typical Spinal Block During Cesarean Delivery

Launched by OREGON HEALTH AND SCIENCE UNIVERSITY · Jan 4, 2024

Trial Information

Current as of June 26, 2025

Enrolling by invitation

Keywords

Spinal Anesthesia Bupivacaine Sensory Dermatomal Level

ClinConnect Summary

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 dermatomal levels will be assessed at 1 (t1), 3 (t3), 5 (t5), 7 (t7), 9 (t9), 11 (t11), 13 (t13), and 15 (t15) minutes after intrathecal 1.6 ml 0.75% bupivacaine in 8.25% dextrose combined with 15 mcg fentanyl and 150 mcg morphine (study solution). Spinal failure, which is defined as inability to achieve a T4 level to pinprick by the 15-minute timepoint or intraoperative pain (VAS \> 0) requiring trea...

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • 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 Criteria:
  • 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

About Oregon Health And Science University

Oregon Health and Science University (OHSU) is a leading academic medical center dedicated to advancing health through research, education, and patient care. As a prominent sponsor of clinical trials, OHSU leverages its extensive expertise in various medical fields to facilitate innovative research aimed at improving patient outcomes. The institution is committed to ethical standards and rigorous scientific methodologies, fostering collaborations that enhance the development of new therapies and interventions. With a focus on translating research discoveries into clinical practice, OHSU plays a pivotal role in shaping the future of healthcare.

Locations

Portland, Oregon, United States

Patients applied

0 patients applied

Trial Officials

Brandon M Togioka, MD

Principal Investigator

Oregon Health and Science University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported