NCT04630171 - VerTouch Device: A Prospective Randomized Controlled Trial | Biotech Hunter

Enrollment

Participants

Timeline

Start Date

January 1, 2021

Primary Completion Date

November 28, 2023

Study Completion Date

November 29, 2023

Conditions

PregnancyPain

Interventions

DEVICE

Group #1: VerTouch utilized for identification of site for labor epidural or spinal anesthesia procedure

Group #1: VerTouch utilized for identification of site for labor epidural or spinal anesthesia procedure for women requesting labor analgesia

DEVICE

Group #2: Ultrasound (US) utilized for identification of site for labor epidural or spinal anesthesia procedure

Group #2: Ultrasound (US) utilized for identification of site for labor epidural or spinal anesthesia procedure for women requesting labor analgesia

OTHER

Group #3: Control group, palpation utilized for identification of site for labor epidural or spinal anesthesia procedure

Control group, palpation utilized for identification of site for labor epidural or spinal anesthesia procedure for women requesting labor analgesia

Trial Locations (1)

Northwestern Memorial Hospital and Prentice Women's Hospital, Chicago

All Listed Sponsors

collaborator

Intuitap

UNKNOWN

lead

Northwestern University

OTHER