Sponsor:
Benaroya Research Institute
Code:
NCT03843879
Conditions
Postoperative Pain
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Accepted
Interventions
Transversus Abdominis Plane Block
Intravenous Lidocaine
Brief summary:
Conditions
Postoperative Pain
Study ID
NCT03843879
Start date
Apr 1, 2019
Status verified date
Jul, 2019
Completion date
Sep 1, 2021
Anticipated
Primary completion date
Mar 1, 2021
Anticipated
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Accepted
Enrollment
124 participants
Anticipated
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary purpose
Treatment
Arms
active comparator: TAP Block
active comparator: IV Lidocaine
Interventions
Transversus Abdominis Plane Block
Intravenous Lidocaine
Primary outcome measure
Central contacts
Locations
Virginia Mason Medical Center
Recruiting
Seattle, Washington, United States, 98101
Contacts
Neil A Hanson, MD
neil.hanson@virginiamason.orgWyndam M Strodtbeck, MD
wyndam.strodtbeck@virginiamason.orgSponsor
Benaroya Research Institute
Last update posted
Jul 17, 2019
Last verified
Jul, 2019
Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Benaroya Research Institute on 2019-07-17.