Multiple Sclerosis Trial, Recruiting NCT06782464 Sponsor: Centre National de Rééducation Fonctionnelle et de Réadaptation Condition: Multiple Sclerosis
Back to Multiple Sclerosis

Multiple Sclerosis Trial, Recruiting

NCT06782464
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are over 18 years old
  • People whose overall health condition is stable and not changing significantly
  • People who have muscle stiffness and weakness on one side of the body (arm) caused by a stroke, brain injury, or lack of oxygen to the brain, where that event happened more than 6 months ago
  • People whose affected arm shows significant stiffness in the shoulder muscles that pull the arm inward or rotate it inward, at a level measured at 1+ or higher on a standard stiffness scale
  • People who have a pain level greater than 40 out of 100 on a standard pain rating scale
  • People whose arm stiffness makes it difficult for caregivers to assist with daily care tasks
  • People who have the mental capacity to understand the study and make their own decisions about taking part
  • People who are on a stable, unchanged medication schedule
  • People who are able to take part in a rehabilitation program and attend scheduled assessment sessions throughout the study

Who may not be able to join:

  • People where, in the trial doctor's opinion, taking part would put them at an unacceptable health risk
  • People who have had a previous procedure or condition that changed the nerve structure in the affected arm
  • People who have had any injection into the affected arm (such as nerve-blocking, scarring, or anaesthetic injections) within the last 4 months
  • People who are currently receiving an invasive treatment for muscle stiffness, such as a medication pump delivering medication directly to the spinal fluid
  • People who are already enrolled in another clinical trial for a drug or device aimed at treating muscle stiffness
  • People who are pregnant or breastfeeding
  • People who have an allergy or intolerance to local anaesthetic or to botulinum toxin (a medication used to reduce muscle stiffness)
  • People who have certain medical conditions that make botulinum toxin unsafe, including Myasthenia Gravis or Eaton-Lambert syndrome, or who are taking certain medications that may interact with botulinum toxin (such as a class of antibiotics called aminoglycosides) (confirm with trial site)
  • People who have a skin condition at the area where treatment would be applied that could affect the treatment or its results
  • People taking ongoing medications (prescription or non-prescription) that, in the trial doctor's opinion, could affect their safety or the study results
  • People who have certain conditions that make a cold-based nerve treatment (cryoneurolysis) unsafe, including: a condition where abnormal proteins in the blood react to cold (cryoglobulinemia), a condition where red blood cells are broken down by cold temperatures (paroxysmal cold hemoglobinuria), a skin reaction to cold (cold urticaria), a condition causing reduced blood flow to fingers and toes in the cold (Raynaud's disease), any form of nerve damage in the limbs (peripheral neuropathy), or open or infected wounds on the affected arm
  • People who have a progressive neurological disease, such as ALS (also known as motor neurone disease)
  • People who, in the trial doctor's opinion, may not be suitable for other reasons, such as a history of not following medical instructions, substance addiction, or an unrelated injury to the affected arm

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 23 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: +35226984010

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Centre National de Rééducation Fonctionnelle et de Réadaptation
Registry
ClinicalTrials.gov
Start date
12 December 2024
Est. completion
12 December 2028

Where this trial is recruiting

🇱🇺 Luxembourg

Primary endpoints

Change in active Range of motion shoulder; Change in passive range of motion of shoulder

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov