Using MSOT to Diagnose and Monitor Neuromuscular Diseases in Children
Official title: Multispectral Optoacoustic Imaging (MSOT) as Non-invasive Biomarker for Diagnosis and Monitoring of Neuromuscular Diseases (MSOT-NMD)
Run by Children's Hospital of Eastern Ontario · NCT06438965 · Data updated 2026-11-12
This study is testing a new type of scan to see if it can help doctors diagnose and track the progress of neuromuscular diseases in children without needing invasive procedures.
Quick facts
| Study type | Observational |
|---|---|
| Ages | Any age to 18 Years |
| Sex | All |
| Enrollment | 240 (estimated) |
| Sponsor | Children's Hospital of Eastern Ontario Academic / other |
| Locations | 1 site (Ottawa, Ontario) |
| Status | Recruiting |
| Started | February 7, 2025 |
| Main results expected | July 2027 |
| Study ends | July 2028 |
| Registry record updated | February 12, 2025 |
| Trial ID | NCT06438965 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are children aged from birth to 18 years with a confirmed or suspected diagnosis of a neuromuscular disease.
✕Probably not a fit
Patients with conditions not consistent with a neuromuscular disease or those with active skin lesions may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to evaluate the effectiveness of Multispectral Optoacoustic Tomography (MSOT) as a non-invasive biomarker for diagnosing and monitoring neuromuscular diseases (NMDs) in children. MSOT scans will be performed on muscle regions to assess hemo/myoglobin, collagen, lipid content, and oxygenation levels in patients with confirmed or suspected NMDs. The study will correlate MSOT data with existing clinical, laboratory, and imaging data from standard care procedures over a period of approximately 36 months, with repeated measurements to track disease progression.
Why it matters
Potential benefit: If successful, this approach could provide a non-invasive method for diagnosing and monitoring neuromuscular diseases in children, potentially improving patient care.
How similar studies have gone: While the use of MSOT in this context is relatively novel, similar imaging techniques have shown promise in other areas of medical diagnostics.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: Patients with neuromuscular disease * Children (from birth (infants that are born term) to 18 years of age) participants or consent through authorized guardian * Confirmed or suspected diagnosis of a neuromuscular disease (through molecular genetics, biopsy, clinical examination) Exclusion Criteria: Participants: * Diagnosis is not consistent with a confirmed or suspected neuromuscular disease * Patients with active skin lesions (e.g. infections, trauma) or confirmed genetic disorders (e.g. epidermolysis bullosa) that predisposes to skin lesion * Medically unstable patients * Tattoo on skin overlying the area to be examined * Missing consent form * Exclusion due to safety concerns of the investigator (subject who has any condition, including any physical, psychological, or psychiatric condition, which in the opinion of the Investigator, would compromise the safety of the subject or the quality of the data and renders the subject an unsuitable candidate for the study) * Medication leading to increased light sensitivity
Where it's running
-
Cheo
Ottawa, Ontario, Canada Recruiting
Study contacts
- Study coordinator: Hanns Lochmuller, Dr.
- Email: hlochmuller@toh.ca
- Phone: (613) 737-7600
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.