Massage gun vs. hands: which eases Post-Hip-Surgery numbness?

NCT ID NCT07790705

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Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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 Results may not be published yet.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
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)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
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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

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Status unknown
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First seen Aug 27, 2026 · Last updated Sep 09, 2026 · Updated 2 times

Summary

After hip replacement through a front incision, many people feel numbness, tingling, or burning in the thigh because a nearby nerve gets irritated. This trial tests whether a handheld massage gun, used at home twice a day for six weeks, can ease those symptoms faster than gentle hand massage. Adults scheduled for a first hip replacement will be randomly assigned to one of the two routines. Researchers will compare hip pain, function, numbness, and sleep quality at six weeks and three months after surgery.

What this could mean

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

Active substance
A handheld percussive massage device (massage gun) self-applied to the thigh
What this could lead to
If it works, this could give hip replacement patients a simple, at-home way to recover faster and reduce lingering numbness and pain.
What could go wrong
This is a small, early-stage trial, and the massage gun may not outperform gentle hand massage. There is also a risk of discomfort or bruising from the device.

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

About 58 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Jan 2027

An estimate. End dates often move.

Lead sponsor

A research network

The lead sponsor is a research network or cooperative group.

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

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Age 18 years or older at the time of surgery * Scheduled for primary unilateral elective anterior total hip arthroplasty for osteoarthritis, avascular necrosis, or inflammatory arthritis * Sufficient upper extremity strength and hand dexterity to perform either intervention independently, OR a reliable caregiver willing and able to assist with sessions throughout the 6-week period * Able to provide written informed consent * Willing and able to perform twice-daily sessions, maintain a daily log, and attend follow-up visits at Week 6 and Month 3 * Body mass index (BMI) less than 40 kg/m² Exclusion Criteria: * Revision arthroplasty or prior ipsilateral hip surgery * Pre-existing neurological condition affecting the ipsilateral anterior or lateral thigh, including peripheral neuropathy, lumbar L2-L4 radiculopathy, meralgia paresthetica, or diabetic amyotrophy * Confirmed or history of deep vein thrombosis or pulmonary embolism * Active wound infection, breakdown, dehiscence, or open incision at any treatment session timepoint * Coagulopathy, bleeding disorder, or supratherapeutic anticoagulation at time of enrollment * Active malignancy involving the hip or ipsilateral femur * Concurrent enrollment in another interventional trial * Significant cognitive impairment precluding safe self-administration or valid patient-reported outcome completion * Anticipated contralateral total hip arthroplasty within the 3-month follow-up window

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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.

How to take part

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  1. The places running it

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Contacts and locations

Locations

  • Total Joint Specialists

    Cumming, Georgia, 30041, United States

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