Can a simple patch replace opioids for broken ribs in seniors?
NCT ID NCT05714631
First seen Jul 08, 2026 · Last updated Jul 09, 2026 · Updated 1 time
Summary
This trial investigates whether lidocaine patches can help older adults (65+) with rib fractures use fewer opioids while maintaining pain control. Participants receive either a lidocaine patch, a placebo patch, or standard care. The study measures opioid use and pain scores during their hospital stay. Results could support using lidocaine patches to reduce opioid risks or, if no benefit is found, discourage their use as unnecessary.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- 4% Lidocaine Patch
- What this could lead to
- If effective, lidocaine patches could reduce opioid use and improve recovery in older adults with rib fractures, lowering risks of addiction and side effects.
- What could go wrong
- This is a small, early-phase trial with only 5 participants, so results may not apply broadly. Lidocaine patches may not reduce pain or opioid use more than a placebo.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
5 people
The number who actually took part.
- Started
-
Oct 2023
- Finished
-
Aug 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
65 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * age\>/= 65 years * Patients with injuries meeting an AIS score \</=2 * Patients admitted to trauma service * Patients able to consent Exclusion Criteria: * Age \<65 years * Unable to consent * Chronic pain medication usage; defined as \>/= 3 weeks of \>/= 30 mg oral morphine equivalent * History of allergic reaction to lidocaine or adhesive tape * Prisoners * Patient will be excluded if pain is worse in non-ribs location * Patient will be excluded if he has injuries not meeting our criteria
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Abdul Hafiz Al Tannir
Milwaukee, Wisconsin, 53213, United States
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Other studies related to the condition(s) this trial covers.
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