UnknownPhase 4ketamine

US-guided SAPB for Rib Fractures in the ED

Sponsored by Andrew A Herring

NCT ID
NCT03619785
Target Enrollment
70 participants
Start Date
2018-11-06
Est. Completion
2019-08-31

About This Study

The purpose of this randomized controlled study is to determine whether the serratus anterior plane block reduces pain more than the usual treatment for rib fractures in the same amount of time.

Conditions Studied

Rib FracturesRib Fracture Multiple

Interventions

  • Bupivacaine
  • Fentanyl, morphine, hydromorphone, hydrocodone, acetaminophen, ketorolac, gabapentin, ketamine, ibuprofen

Eligibility

Age:18 Years - N/A
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Males and females 18 years and older, capable of providing informed consent indicating awareness of the investigational nature of the study, in keeping with institutional policy.
* Written informed consent must be obtained from each patient prior to entering the study.
* Patients with moderate to severe pain (NRS 4 to 10) as a result of one or more rib fractures occurring at levels T2-T8, measured on a self-reported NRS.

Exclusion Criteria:

* Patient refusal
* Patients with significant pain from other injuries (as determined at the discretion of the treating physician)
* Patients deemed critically ill by provider
* Patients with decompensated psychiatric disorders
* Pregnant patients (positive urine or serum B-HCG)
* History of heart block or bradycardia
* History of uncontrolled seizures
* Patients allergic to lidocaine, bupivacaine, ropivacaine, or morphine
* Patients with bilateral rib fractures

Study Locations (1)

Alameda Health System - Highland Hospital
Oakland, California, United States

This trial is not recruiting

This study is currently not accepting new participants.

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Data Source
ClinicalTrials.gov

Last updated from source

US-guided SAPB for Rib Fractures in the ED | Huxley