New needle treatment may replace surgery for stubborn tennis elbow

NCT ID NCT02710682

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 This study
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 Results may not be published yet.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)

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This status has not been confirmed recently, so it may be out of date.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 Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This study tests if a less invasive ultrasound-guided needle procedure can work as well as mini-open surgery for chronic tennis elbow that hasn't improved with rest or therapy. Sixty-four workers with persistent elbow pain will be randomly assigned to one of the two treatments. The main goal is to see which approach better reduces pain and improves function after six months.

What this could mean

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

Active substance
Ultrasound-guided tendon fenestration (minimally invasive procedure) and mini-open surgery
What this could lead to
If successful, this could show that a less invasive ultrasound-guided procedure works as well as surgery for chronic tennis elbow, offering a quicker recovery option.
What could go wrong
This is a small pilot study with only 64 participants, so results may not apply to everyone. The ultrasound technique is still experimental and may not be as effective as surgery.

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

64 people

The number who actually took part.

Started

Jun 2016

Finished

Jul 2020

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

30 to 67 years

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: * Workers * Ability to read, understand and answer questionnaires in French or English * Diagnosis of unilateral, lateral epicondylosis established by an orthopaedist, determined by clinical presentation and pain, ≥ 4/10 on a pain numerical rating scale, on palpation of the region slightly anterior and distal to the lateral epicondyle, exacerbated by the extension of the wrist or the middle finger when the elbow is in extension. * Chronic epicondylosis, refractory to medical treatment conducted for at least six months, which includes rest and implementation of ergonomics to avoid soliciting the extensor tendons, and at least one of: physical therapy, a rehabilitation program with stretching and / or strengthening exercises, injection treatments (corticosteroids, autologous PRP) or extracorporeal shock waves. Exclusion Criteria: * Suspected tumor or infectious etiology * Injection of corticosteroids during the last 3 months * Hemorrhagic diathesis; anticoagulation (platelets \<50,000, International Normalized Ratio (INR) \> 2) * Local infection * History of elbow surgery or fracture * History of inflammatory arthropathy * Neck pain and radiculopathy * Inability to provide informed consent because of a language problem, dementia or a major psychiatric disorder.

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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

  • Centre hospitalier de l'Université de Montréal

    Montreal, Quebec, H2X 0C1, Canada

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