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NCT03571919: Lidocare

Lidocaine Infusions for Rib Fractures

Withdrawn Phase 4 Last updated 28 June 2021
What this trial tests

Phase 4 trial testing Lidocaine infusion in Rib Fracture Multiple. Withdrawn.

Timeline
15 June 2018
Primary endpoint
1 June 2019
1 July 2019

Quick facts

Lead sponsorStanford University
PhasePhase 4
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Start date15 June 2018
Primary completion1 June 2019
Estimated completion1 July 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Stanford University

Who can join

18 and older, any sex, with Rib Fracture Multiple or Trauma Chest. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Patients with traumatic rib fractures not receiving regional anesthesia through a epidural or nerve block catheter will be recruited for the study. Once enrolled, they will be randomized to receive either intravenous lidocaine or intravenous saline for control of pain related to their rib fractures. In addition, they will receive other pain medications, such as acetaminophen, gabapentin, and opioid pain medications. Our primary outcome is a decrease in their opioid medication requirements.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Lidocaine infusion

Trials testing the same drug.

Other recruiting trials for Rib Fracture Multiple

Currently open trials in the same condition.

Other Stanford University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03571919.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing