A new standard for pain pills after kidney stone surgery?
NCT ID NCT05353478
First seen Aug 11, 2026 · Last updated Sep 18, 2026 · Updated 2 times
Summary
This study tests whether a standardized approach to prescribing opioid pain medication after percutaneous nephrolithotomy (PCNL), a surgery to remove kidney stones, can reduce the number of unused painkillers patients take home. Researchers will compare the usual prescribing habits with a set protocol to see if it leads to fewer leftover opioids and fewer unfilled or refilled prescriptions. The goal is to find a balance that manages pain effectively while avoiding overprescription.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A standardized opioid prescribing protocol
- What this could lead to
- If successful, this could establish a safer standard for prescribing painkillers after kidney stone surgery, reducing unused opioids and the risk of misuse.
- What could go wrong
- The trial is small and early, and results may not apply to all hospitals. Some patients might still need more pain relief than the standard plan provides.
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.
- Participants
-
80 people
The number who actually took part.
- Started
-
Jun 2022
- Expected to finish
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Aug 2027
An estimate. End dates often move.
- Lead sponsor
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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.
Who is studied
Subjects undergoing percutaneous nephrolithotomy at Mayo Clinic Rochester.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: \- Patients undergoing percutaneous nephrolithotomy at Mayo Clinic Rochester. Exclusion Criteria: * Unable or unwilling to provide informed consent. * Patients who require Intensive Care Unit admission after surgery. * Patients who have Clavien grade III or greater postoperative complications requiring additional intervention \< 30 days after index procedure.
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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
-
Mayo Clinic Rochester
Rochester, Minnesota, 55905, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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