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New injection technique offers hope for stubborn neck pain sufferers

NCT ID NCT07503574

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested two types of injections for people with long-lasting neck pain caused by muscle knots that didn't get better with usual treatments. 96 adults received either a dextrose solution or a lidocaine-saltwater mix injected between layers of tissue under ultrasound guidance. The goal was to see which injection worked better for reducing pain, improving neck movement, and enhancing daily life over three months.

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

96 people

The number who actually took part.

Started

Apr 2025

Finished

Aug 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 to 65 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: * Patients aged 18-65 years old * Chronic neck pain associated with MAS in the upper trapezius for at least 3 months and a VAS score above 5 * Compliance with the MAS criteria defined by Travel and Simons (five major and one minor criterion) * Lack of response to conservative treatment methods such as medical and physical therapy for neck pain * Willingness to participate in the study Exclusion Criteria: * Previous surgery on the shoulder or cervical region * History of neck and shoulder trauma * Presence of fibromyalgia syndrome * Presence of cervical radiculopathy or shoulder pathologies * Patients who have undergone injection or physical therapy program within the last three months * History of lidocaine allergy * Presence of coagulopathy * Presence of rheumatological and neurological diseases * Patients with uncontrolled diabetes mellitus * Presence of severe psychiatric comorbidity * Presence of local or systemic infection * Presence of needle phobia

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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

  • Ankara Training and Research Hospital

    Ankara, Ankara, 06010, Turkey (Türkiye)

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Other studies related to the condition(s) this trial covers.