Efficacy of continuous intercostal nerve block for patients with multiple rib fractures

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study evaluates the effectiveness of continuous intercostal nerve block (CINB) combined with medical therapy compared to standard medical care for patients with multiple rib fractures. It is a prospective, randomized, non-blinded trial that aims to assess pain management outcomes in patients admitted to the trauma service. Participants will receive either CINB with additional pain management or standard treatment involving nonsteroidal anti-inflammatory drugs and opioids. The goal is to determine if CINB provides superior pain relief and improves recovery.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Subjects will be at least 18 years old
* Subjects will have 2 or more identified rib fractures
* Subjects will be willing to provide informed consent for procedure
* Subjects will be identified as appropriate for initiation of continuous nerve block therapy for treatment of rib fracture associated pain.

Exclusion Criteria:

* Documented allergy to study medication
* Epidural catheter use
* Prisoners
* Refusal of CINB therapy

Where it's running

• University of Kentucky Medical Center
  Lexington, Kentucky, United States Recruiting

Study contacts

• Principal investigator: Zachary Warriner, MD — University of Kentucky

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.