Abdominal Wall Block Study

NACompletedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

August 7, 2017

Primary Completion Date

July 12, 2021

Study Completion Date

July 12, 2021

Conditions
Umbilical HerniaObesity
Interventions
PROCEDURE

TAPB Group

Subjects allocated to the TAPB group will be monitored for instances of intraoperative local anesthetic supplementation, analgesic administration, or conversion to general anesthesia will be compared.

PROCEDURE

RSB Group

Subjects allocated to the RSB group will be monitored for instances of intraoperative local anesthetic supplementation, analgesic administration, or conversion to general anesthesia will be compared.

PROCEDURE

conversion to general anesthesia

For those who do not respond to TAPB or RSB to allow for completion of the intended procedure.

Trial Locations (1)

32608

Malcom Randall VA Medical Center, Gainesville

All Listed Sponsors
collaborator

US Department of Veterans Affairs

FED

lead

University of Florida

OTHER

NCT03074240 - Abdominal Wall Block Study | Biotech Hunter | Biotech Hunter