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Could a nerve block boost frozen shoulder treatment?
NCT ID NCT07680504
First seen Jul 02, 2026 · Last updated Jul 02, 2026
Summary
This study compares two treatments for frozen shoulder (retractile capsulitis): a standard steroid injection into the shoulder joint versus that same injection plus a nerve block near the shoulder blade. The nerve block uses a numbing medicine and a steroid to calm the nerve that supplies the shoulder. Researchers want to see if the combination improves shoulder function more than the injection alone over three months. About 38 adults with shoulder pain and stiffness lasting 2 to 12 months will take part.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- betamethasone (Diprostene) and lidocaine
- What this could lead to
- If it works, this combination approach could offer better pain relief and faster recovery for people with frozen shoulder.
- What could go wrong
- This is a small, early-phase pilot study, so results may not apply to everyone. The nerve block itself carries rare risks like bleeding or nerve damage.
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
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 38 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2029
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.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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 with shoulder pain and stiffness that has persisted for at least 2 months but less than 12 months, with a loss of passive range of motion in at least 2 planes (lateral rotation, medial rotation, abduction, forward flexion) of at least 30 degrees compared to the contralateral side * Patients between the ages of 18 and 65 * Patients enrolled in a social security program Exclusion Criteria: * \- Corticosteroid injection into the affected shoulder \< 4 months ago * History of any surgery on the affected shoulder within the past 12 months * Patients with a neuromuscular condition (neurological deficit) or shoulder condition (arthropathy) that could interfere with the assessment of the primary endpoint * Signs or risk of infection (bacterial-like infection and/or fever and/or antibiotic use) * Poor skin condition of the affected shoulder * Anticoagulation with VKAs or anti-Xa agents, or active bleeding disorder or one in remission for less than 5 years (malignant hematologic disorders, myelodysplasia, autoimmune thrombocytopenia) or chemotherapy (antiplatelet agents permitted except prasugrel and clopidogrel)\* * Uncontrolled hypertension, * Decompensated diabetes or diabetes at risk of decompensation, * Contraindications to diprosten, Kenacort, or lidocaine * Psychiatric conditions that may be exacerbated by corticosteroids * Pregnant or breastfeeding women, or women who refuse to use effective contraception * Individuals belonging to a vulnerable group as defined by Regulation (EU) No. 536/2014 and French law (See section 4.4 of the protocol) - - Patients unable to comply with the protocol requirements (see Section 4.4 of the protocol) * Patients participating in another clinical research protocol involving a drug or medical device * Patients who refuse to participate in the study
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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
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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CHU de Nantes
Nantes, France