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Use of Ultrasound Guidance to Assist With Labor Epidural Placement in Patients With a BMI ≥40

T

Thomas J. Vernon

Status

Completed

Conditions

Labor Pain

Treatments

Device: Ultrasound
Other: Palpation

Study type

Interventional

Funder types

Other

Identifiers

NCT02984267
OBUS1123

Details and patient eligibility

About

Placement of labor epidurals is a very common daily practice in obstetrical anesthesia. Currently, these epidurals are placed based upon palpation of landmarks to determine midline and the correct spinal level for placement. Palpation of these landmarks can be difficult, however, particularly in morbidly obese patients who have significant amounts of soft tissue overlying them. This study seeks to use ultrasound guidance to examine the spine prior to epidural placement, and see what effects this has compared to palpation alone with respect to procedure time, number of attempts, success rate in the first attempt, failure rate, complication rate, patient anxiety levels, and patient satisfaction levels.

Enrollment

18 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Current (pregnant) BMI ≥ 40
  • Age ≥ 18
  • ASA score of 3 or less
  • Full term pregnancy (37 weeks gestational age or greater)

Exclusion criteria

  • Known scoliosis
  • Known contraindications to neuraxial blockade
  • Intrauterine fetal demise or non-viable fetus.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

18 participants in 2 patient groups

Ultrasound Group
Experimental group
Description:
The interventional group that will have their spine evaluated by ultrasound prior to epidural placement
Treatment:
Device: Ultrasound
Palpation Group
Other group
Description:
The control group that will have their epidural placed in the usual fashion based on palpation
Treatment:
Other: Palpation

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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