Could a massage gun help clear kidney stone fragments after surgery?

NCT ID NCT05872230

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early This study
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jul 07, 2026 · Last updated Jul 08, 2026 · Updated 1 time

Summary

This study tests whether a massage percussion device can help people pass tiny kidney stone fragments left behind after a common stone-removal surgery. After surgery, small fragments often remain in the kidney and may not pass on their own, sometimes requiring another procedure. Participants will use the massage device on their back or side to see if it helps move the fragments out. The trial focuses on whether people can tolerate the therapy and whether it improves the rate of becoming stone-free.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Massage Percussion Therapy device
What this could lead to
If effective, this could offer a simple, non-invasive way to help people pass leftover kidney stone fragments after surgery, reducing the need for additional procedures.
What could go wrong
This is a very small, early feasibility study with only 13 participants. The therapy may not improve stone passage and could cause discomfort or be poorly tolerated.

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

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

13 people

The number who actually took part.

Started

Feb 2024

Finished

May 2025

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

18 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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Any patient after treatment of renal stones with ureteroscopy during which residual stone fragments (less than 2mm by surgeon estimation) is left in the kidney. * Must be 18 years or older * Must be able to give consent * Preoperative abdominal CT Exclusion Criteria: * On pharmacologic anticoagulation. Aspirin up to 81mg will be allowed. * Cannot tolerate flank, prone or Trendelenburg position. * Cannot tolerate percussion. * History of acute rib fractures or osteopenia/osteoporosis. * Any patient who is on a fluid intake restriction. * Pregnancy * Untreated UTI * History of struvite stones * Requiring a planned secondary stone procedure within 90 days * If stent must stay in longer than 10 days * Ureteral stones (without renal stones)

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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

  • University of Montreal

    Montreal, Canada

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