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临床试验/NCT07362875
NCT07362875招募中不适用

Development of Quantitative Muscle Imaging as a Biomarker of Disease Endpoints in Myotonic Dystrophy (DeQoDE-DM)

Wake Forest University Health Sciences1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2025年5月15日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
75
试验地点
1
主要终点
Contractile muscle volume (CMV, cm3)

研究概览

简要总结

Myotonic dystrophy (dystrophia myotonica; DM), the most prevalent form of muscular dystrophy in adults, is characterized by progressive myopathy, myotonia, and multi-systemic involvement. DM causes severe disability and profoundly affects the patient's quality of life. Currently, no effective treatments are available that alter the course of the disease, but ongoing clinical trials are underway.

详细描述

Past and current clinical trials in DM1 have relied on muscle biopsies to evaluate pathology and measure drug activity. However, this method is invasive and inefficient for long-term monitoring. What is lacking are non-invasive imaging biomarkers capable of providing comparable data, which would enhance trial planning, accelerating drug development while reducing morbidity and costs. Non-invasive muscle imaging, particularly through Quantitative Magnetic Resonance Imaging (qMRI), is essential to better understand how DM affects muscle structure. Moreover, the relationships between Magnetic Resonance Imaging (MRI) measures, disease severity, and Ribonucleic Acid (RNA) splicing outcomes from muscle tissues in the same DM patients are not yet known. As MRI has been relatively unstudied in DM, there needs to be a comprehensive baseline characterization of muscle structure and its relationship to clinical endpoints and RNA-associated disease processes. This will help evaluate the potential of qMRI as a biomarker of disease severity in DM.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • DM subjects
  • Age 18 - 65 years
  • Diagnosis of DM1 or DM2 by clinical or genetic criteria. If DM1 or DM2 was diagnosed by clinical criteria, a first-degree relative must have genetic testing confirmation and sign a genetic consent form to release their genetic information
  • Clinically affected, as defined by muscle weakness or myotonia
  • Ambulate independently (a walker is not permitted)
  • Able to provide informed consent for participation in the study
  • Control subjects
  • Age 18 - 65 years old
  • Healthy as defined by no significant medical or neurological conditions
  • Able to provide informed consent for participation in the study

排除标准

  • Cardiac pacemaker, defibrillator, metal implants, or other contraindications for MRI
  • Use of anabolic or catabolic agents within one year of entry
  • History of lumbar spine or leg surgery, lumbar radiculopathy, or peripheral neuropathy
  • BMI > 35 because obesity compromises positioning on the MR scanner
  • Pregnancy
  • For muscle biopsy, history of bleeding disorders or on anticoagulation. Subjects taking nonsteroidal anti- inflammatory agents will be asked to discontinue these medications 7 days prior to muscle biopsy.

研究组 & 干预措施

Control subjects

  1. Age 18 - 65 years old
  2. Healthy as defined by no significant medical or neurological conditions
  3. Able to provide informed consent for participation in the study

DM subjects

  1. Age 18 - 65 years
  2. Diagnosis of DM1 or DM2 by clinical or genetic criteria. If DM1 or DM2 was diagnosed by clinical criteria, a first-degree relative must have genetic testing confirmation and sign a genetic consent form to release their genetic information.
  3. Clinically affected, as defined by muscle weakness or myotonia
  4. Ambulate independently (a walker is not permitted)
  5. Able to provide informed consent for participation in the study

结局指标

主要结局

Contractile muscle volume (CMV, cm3)

时间窗: Baseline

Contractile muscle volume (CMV, cm3) of individual muscles and the total CMV within the thigh (anterior, medial, posterior) and calf (anterior, lateral, posterior) compartments

Muscle fat fraction (MFF, %)

时间窗: Baseline

Muscle fat fraction (MFF, %) of individual muscles and the total CMV within the thigh (anterior, medial, posterior) and calf (anterior, lateral, posterior) compartments

次要结局

  • Average measures of Manual muscle testing (MMT)(Baseline)
  • Average measures of Quantitative Muscle Testing (QMT)(Baseline)
  • Average measures of grip strength (pounds or kilograms)(Baseline)
  • Average measures of pinch strength(Baseline)
  • The 6-minute walk test (6MWT) times(Baseline)
  • gait speed times(Baseline)
  • step test amount(Baseline)
  • sit-to-stand test amount(Baseline)
  • Short Physical Performance Battery (SPPB) Scores(Baseline)
  • Nine-Hole Peg Test (9HPT) times(Baseline)
  • Time Up and Go (TUG) times(Baseline)
  • DM1-Activity and Participation Scale (DM1-Activ) Scores(Baseline)
  • Patient-Reported Outcomes Measurement Information System (PROMIS-10) Scores(Baseline)
  • Brief Pain Inventory (BPI) Scores(Baseline)
  • Checklist Individual Strength (CIS-fatigue) Scores(Baseline)
  • Muscular Impairment Rating Scale (MIRS) Scores(Baseline)
  • presence of edema-liked changes(Baseline)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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