CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 128 enrolled
Drug / intervention
Rivanna Accuro US Device +3 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03214640
NCT03214640N/ACompleted

Evaluation of Success in Neuraxial Block Placement Between Using Palpation of Landmark Versus Pocket-Size Handheld Ultrasound (U/S) Method

Wake Forest University Health Sciences·interventional·Posted Jul 11, 2017·Updated Jul 28, 2021

In Brief

A clinical study evaluating Rivanna Accuro US Device, Palpation, and 2 other interventions for Analgesia. Completed, enrolled 128 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAnalgesia
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedJul 11, 2017
Enrollment StartOct 23, 2017
Primary CompletionApr 13, 2019
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 9.0 years ago

Interventions

Rivanna Accuro US Devicedevice

When the subject is ready for neuraxial procedure, the location for the epidural or spinal needle insertion will be identified with Rivanna Accuro U/S device. For subjects in group C-R or L-R, the needle insertion site will be the site identified by the Rivanna Accuro U/S device. After placement of spinal for Cesarean or epidural for labor, the usual standard dose of medication will be administered as in usual manner for patients regardless in this study or not.

Palpationother

When the subject is ready for neuraxial procedure, the location for the epidural or spinal needle insertion will be identified with Palpation method using conventional landmarks (spinous process and iliac crest). For subjects in group C-P or L-P, the needle insertion site will be the site identified by the Palpation method. After placement of spinal for Cesarean or epidural for labor, the usual standard dose of medication will be administered as in usual manner for patients regardless in this study or not.

Neuraxial Analgesiaprocedure

Labor analgesia will be provided utilizing the standard medications to provide labor analgesia

Spinal Blockprocedure

Spinal anesthetic medications will be utilized in providing surgical block for cesarean delivery as is standard of care