NCT06782464Recruiting
Upper Limb Nerve Cryoneurolysis is Non Inferior to the Usual Care and Has Therapeutic Add Value in Dealing With Shoulder Pain and Functional Problems Caused by Spasticity and Motor Impairment
Ultrasound Guided Cryoneurolysis to Treat Shoulder Pain and Functional Problems Related to Upper Limb Spasticity
Source: ClinicalTrials.gov · Last updated 19 Mar 2026
Brief summary (registry, in English)
This trial is part of the spastiCRYO clinical research project. The primary objective of this clinical trial is to test the hypothesis: "Upper limb nerve cryoneurolysis is non inferior to the usual care and has therapeutic add value in dealing with shoulder pain and functional problems caused by spasticity and motor impairment". It is a non-inferiority study on the referred topic, comparing the therapeutic effect (improvement in function and pain) of cryoneurolysis of selected nerves (lateral pectoral nerve and thoracodorsal nerve) with the usual care: intramuscular botulinum neurotoxin type A (BoNT-A) injection of pectoralis major, teres major and subscapularis muscles. The hypothesis is that cryoneurolysis is not inferior to the usual care in terms of magnitude of the therapeutic effect and might have a therapeutic add-value in terms of duration of that effect. Two secondary hypotheses are firstly, that cryoneurolysis is a safe procedure that can be deployed in a rehabilitation hospital setting with minimum requirements to perform mini-invasive procedures and secondly that selecting patients who might benefit from this treatment is straightforward. To test these hypotheses, the research team will gather, analyse and compare outcome measures data from the endpoints which are the changes along the trial duration in shoulder pain, upper limb function, involved muscles spasticity, shoulder range of motion (abduction and external rotation) level of impairment, and follow-up of potential adverse effects in two independent and equivalent groups of participants who have shoulder pain and functional limitations caused by spasticity and are in a stable phase of their condition. Participants in one group (cryoneurolysis arm) have one session of selected nerves ultrasound and neurostimulation guided cryoneurolysis and participants in the other group (BoNT-A arm) have one session of ultrasound and neurostimulation guided injection of BoNT-A in the pectoralis major, teres major and subscapularis. The participants of the two groups follow an upper limb analogous rehabilitation program for 24 weeks after each intervention. Longitudinal follow-up in the trial will take 24 weeks. In a real-world scenario, within 24 weeks the effect of Bont-A intramuscular injection has already waned, and the procedure should be repeated. Secondary objectives are to compare changes in upper limb sensory function and electroneuromyographic parameters with the intention to understand the cryoneurolysis mechanism of action and the reversibility of this mini-invasive intervention. Changes in quality-of-life dimension of participants is a secondary endpoint as well.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- First submitted
- 13 Dec 2024
- Start date
- 12 Dec 2024
- Primary completion date
- 12 Dec 2028
- Lead sponsor
- Centre National de Rééducation Fonctionnelle et de Réadaptation
- Diseases
- Stroke, Multiple sclerosis
- NCT number
- NCT06782464
What you commit to
- Study type: Interventional
- Planned participants: 50
- From 12 Dec 2024 to the primary completion date, 12 Dec 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previous intervention or condition that altered the target neural anatomy of the upper limb.
- Current enrollment in an investigational drug or device study targeting spasticity management.
- Chronic medication use (prescription or over-the-counter) that, in the investigator's opinion, would affect study participation or subject safety.
- Diagnosis of concomitant progressive neurological diseases such as Amyotrophic Lateral Sclerosis.
Other illness
- Allergy or intolerance to local anesthesia/BoNT-A.
- Contraindications to BoNT-A administration, such as:
- Myasthenia Gravis
- Eaton-Lambert syndrome
- Possible drug interactions (e.g., aminoglycosides and BoNT-A)
- Any local skin condition at the treatment site that may adversely affect treatment or outcomes.
- Contraindications to cryoneurolysis, including:
- Diagnosis of cryoglobulinemia
- Paroxysmal cold hemoglobinuria
- Cold urticaria
- Raynaud's disease
- Any form of peripheral neuropathy
- Open and/or infected wounds on the affected limb
- Any reason, in the investigator's opinion, that the subject may not be suitable for study participation (e.g., history of noncompliance, drug addiction, or any related upper limb injury).
Other
- In the investigator's opinion, the subject will be exposed to unacceptable risk by participation.
- Any injection (neurolytic, sclerosing, anesthesia, etc.) to the upper limb within the last 4 months.
- Spasticity invasive treatment such as intrathecal baclofen during the trial.
- Pregnancy or lactation.
Who the study is looking for
- Be over 18 years old.
- Have a clinically and functionally stable condition.
- Present spastic hemiplegia of the upper limb caused by a stroke, traumatic, or hypoxic brain event occurring more than 6 months before the study.
- The paretic upper limb must present significant spastic plegia at the shoulder adductors and/or shoulder internal rotators (≥ 1+ on the Modified Ashworth Scale).
- Have a Visual Analogue Scale (VAS) pain score \> 40/100 mm.
- Have spasticity causing limitations in providing care.
- Have the cognitive capacity to make informed decisions. A comprehensive explanation of the study will be provided orally and in writing to participants and a trusted relative of their choosing.
- Maintain any medications on a stable schedule.
- Accept and have access to an interdisciplinary rehabilitation program and standardized evaluation sessions throughout the study.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Rehazenter, Centre National de Rééducation fonctionnelle et de Réadaptation Coordinator of this site? Confirm its status | Luxembourg | Luxembourg | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.