Rhode Island Hospital
Providence, Rhode Island, 02903, United States
NCT Number: NCT06299137
The goal of this clinical trial is to test the effectiveness of the Serratus Anterior Plane Block in patients with rib fractures. The main questions it aims to answer are:
* Determine if UG-SAPB results in an improved pain, incentive spirometry, and cough ability (PIC) score when compared to usual care over the first five hours. * Evaluate if UG-SAPB results in fewer opioid medications administered when compared to usual care over the first 24 hours.
Participants will undergo the Serratus Anterior Plane. Researchers will compare this to usual care to see if this intervention improves pulmonary function and reduces opioid requirements for ED patients with rib fractures.
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Notify Me18 year and older
All sexes
Interventional
Early Phase 1
Providence, Rhode Island, 02903, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients who undergo randomization to the intervention arm will undergo the Serratus Anterior Plane Block.
For the Serratus Anterior Plane Block, Ropivacaine will be used as the anesthetic.
Other names: Ropivacaine
Time frame: 5 hours
Determine if the SAPB results in an improved pain, incentive spirometry, and cough ability (PIC) score when compared to usual care over the first five hours. The PIC score is a scoring system that can be measured serially in patients with rib fractures to assess pulmonary function and to prognosticate clinical outcomes.
Time frame: 24 hours
Evaluate if UG-SAPB results in fewer opioid medications administered when compared to usual care over the first 24 hours.
Rhode Island Hospital
Other
Ultrasound Guided Serratus Anterior Plane Block in ED Patients With Rib Fractures,
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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