Epidural Placement Using Handheld Ultrasound Device vs. Traditional Landmark Palpation

Labor Pain Clinical Trial

Official title:

Timely Epidural Placement Using Handheld Ultrasound Device vs. Traditional Landmark Palpation in Parturients With Various Body Mass Indices (BMI): A Prospective Randomized Clinical Trial

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT04020042
• Other study ID #: STU-2019-0571
• Status: Terminated
• Phase: N/A
• Start date: August 28, 2019
• Est. completion date: March 23, 2021

Study information

• Verified date: May 2022
• Source: University of Texas Southwestern Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Ultrasound is widely in uses for vascular, nerve block and sometimes neuraxial block. The purpose of the study is to evaluate the impact of a handheld ultrasound device on the time to complete labor epidural placement and success rate of epidural analgesia in parturients with a wide range of body mass indexes (BMIs).

A handheld ultrasound device (Accuro, Rhivanna Medical, Charlottesville, VA) may eliminate the time for equipment setup due to its portability and instant power-up. In addition, it provides a simulated diagram to aid in identifying bone and lumbar spaces. These unique features may be helpful in laboring women with a particular BMI range. We aim to define the usefulness of guidance with a handheld ultrasound in completing labor epidural analgesia in various BMIs.

The primary outcome: The time needed to complete epidural placements.

Secondary outcomes:

• The number of needle insertion attempts,

• The rate of success measured by the need to replacements during the labor course for vaginal or cesarean delivery.

Description:

This randomized prospective clinical trial aims to evaluate timing savings in performing labor epidural analgesia and the success rate of labor analgesia with and without the guidance of a handheld ultrasound device in various BMI groups.

In routine clinical setting, patients admitted to clinic and evaluated labor condition. If patient in active labor and request epidural for labor pain, the standard care team inform obstetric anesthesia epidural team by using pager. Standard of care anesthesia epidural team perform preoperative evaluation and placed the catheter.

The patients in active labor will receive labor epidural analgesia, regardless of the study participation. There is no changes epidural local anesthetic type and doses. The research intervention is only placing hand-hold ultrasound to the back of the patient and see the land mark visually before the epidural catheter placement. The remaining catheter placement is the same as the control group.

Study Procedures:

A Total of 300 eligible parturients will be randomly assigned to one of the two groups either the ultrasound imaging guidance or the traditional landmark palpation group for labor epidural needle placement. The research intervention is simply placing a hand-held ultrasound device on the back of the patient and insert the epidural needle with ultrasound image guidance.

Parturient will receive epidural catheter regardless of the study participation. In the traditional landmark method, anesthetist palpates the structure to determine the site of the initial needle insertion site. The needle will be protruded as in usual standard practice. Anesthetist may remove and insert needle again until feeling epidural space. When anesthetist determine the tip of the needle is in the epidural space, the epidural catheter will be protruded through the needle.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 74
• Est. completion date: March 23, 2021
• Est. primary completion date: March 23, 2021
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Age 18-50 years

• Parturient in active labor and desires labor epidural for pain relief.

• American Society of Anesthesiologists (ASA) Class I, 2 and 3 parturients, which include normal parturients

• Parturients with morbidities (including obesity) that are not life-threatening,

• Parturient BMI = 25

Exclusion Criteria:

• History of scoliosis or back surgery

• Patient refusal

• Patient with elevated intracranial pressure

• Any patient with a contraindication for placement of epidural anesthesia, including infection at needle insertion site, or coagulopathy.

• ASA Class 4

Related Conditions & MeSH terms

• Labor Pain

Intervention

Other:
• Ultrasound image guidance
Epidural landmarks will be determined with using ultrasound image
• Landmark palpation
Epidural landmarks will be determined with palpation

Locations

Country	Name	City	State
United States	Parkland Health Hospital System	Dallas	Texas

Sponsors (1)

Lead Sponsor	Collaborator
University of Texas Southwestern Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The time needed to complete epidural placements	The number of removal and insertion of the epidural needle until feeling epidural space.	Within 10 minutes during epidural needle placement
Secondary	The number of needle insertion attempts	The epidural needle insertion attempts	Within 10 minutes during epidural needle placement