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Spinal Muscular Atrophy clinical trials

View clinical trials related to Spinal Muscular Atrophy.

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NCT ID: NCT04335942 Completed - Clinical trials for Duchenne Muscular Dystrophy

Characterization of the Postural Habits of Wheelchair Users Analysis of the Acceptability of International Recommendations in the Prevention of Pressure Sores Risk by Using a Connected Textile Sensor

Es-Alert
Start date: September 30, 2021
Phase: N/A
Study type: Interventional

Spinal cord injuries and people with Duchenne Muscular Dystrophy or Infant Spinal Muscular Atrophy (ISA) are prone to pain and pressure sores associated with prolonged sitting. For this reason, it is recommended that people with spinal cord injuries release pressure every 15 to 30 minutes and motorized wheelchair users use the electric positioning functions at least 1 minute every hour. The aim is to prevent and/or reduce pain and pressure sores. These devices could help to observe daily the variability of users' pressure maps, their impact on occupational performance, the link with pain and redness and could propose customized adjustments.

NCT ID: NCT04228718 Completed - Clinical trials for Spinal Muscular Atrophy

The Burden of Primary Caregivers of Spinal Muscular Atrophy Patients and Their Needs

Start date: July 1, 2019
Phase:
Study type: Observational

The purpose of this study is to assess carer burden, needs, and expectations of Spinal Muscular Atrophy Parents

NCT ID: NCT04115475 Completed - Clinical trials for Spinal Muscular Atrophy

New Imaging Biomarkers for Muscular Diseases - Multispectral Optoacoustic Imaging in Spinal Muscular Atrophy

MSOT_SMA
Start date: November 7, 2019
Phase: N/A
Study type: Interventional

This study aims to refine the capability of MSOT to characterise muscle tissue and to determine non-invasive, quantitative biomarkers for the disease assessment in patients with spinal muscular atrophy (SMA) using Multispectral Optoacoustic Tomography (MSOT).

NCT ID: NCT03988907 Completed - Clinical trials for Spinal Muscular Atrophy

A Drug-drug Interaction Study With Risdiplam Multiple Dose and Midazolam in Healthy Participants

Start date: June 18, 2019
Phase: Phase 1
Study type: Interventional

This will be a Phase I, 2-part, open-label, non-randomized study to investigate the safety, tolerability, and pharmacokinetics (PK) of a multiple-dosing regimen of risdiplam (Part 1) and the effect of risdiplam on the PK of midazolam (Part 2) following oral administration in healthy adult male and female participants.

NCT ID: NCT03970135 Completed - Clinical trials for Spinal Muscular Atrophy

Fat and Glucose Metabolism in Fed and Fasted State in Patients With Low Skeletal Muscle Mass

Start date: May 29, 2017
Phase: N/A
Study type: Interventional

In a study from 2003 the investigators showed that adult patients with very low skeletal muscle mass (spinal muscular atrophy (SMA) type II, Duchenne muscular dystrophy, congenital muscular dystrophy) are prone to develop hypoglycemia during prolonged fasting. Since then case reports have described the same phenomenon with hypoglycemia and metabolic crises in children with low skeletal muscle mass provoked by infection, fasting and surgery. Pathophysiological mechanisms of metabolism have never been investigated in adults or children with SMA II. Thus the investigators studied fat and glucose metabolism during prolonged fasting in patients with SMA II and LAMA 2 and compared results to those found in healthy controls.

NCT ID: NCT03921528 Completed - Clinical trials for Neuromuscular Diseases

An Active Treatment Study of SRK-015 in Patients With Type 2 or Type 3 Spinal Muscular Atrophy

TOPAZ
Start date: April 22, 2019
Phase: Phase 2
Study type: Interventional

The TOPAZ study will assess the safety and efficacy of SRK-015 in later-onset Spinal Muscular Atrophy (SMA Type 2 and Type 3) in pediatric and adult patients.

NCT ID: NCT03808233 Completed - Clinical trials for Spinal Muscular Atrophy

Reliability and Validity of the ACTIVE-mini for Quantifying Movement in Infants With Spinal Muscular Atrophy

Start date: November 5, 2016
Phase:
Study type: Observational

The purpose of this study is to investigate the measurement properties of the Ability Captured Through Interactive Video Evaluation-mini (ACTIVE-mini) for quantifying movement in infants with Spinal Muscular Atrophy (SMA). Specifically, I will investigate within-day and between-day test-retest reliability and calculate the minimal detectable change of the ACTIVE-mini. Additionally, I will determine the concurrent validity of the ACTIVE-mini with The Children's Hospital of Philadelphia Infant Test for Neuromuscular Disease (CHOP INTEND) and the construct validity of the ACTIVE-mini in infants with SMA using a known group methodology.

NCT ID: NCT03554343 Completed - Clinical trials for Spinal Muscular Atrophy

Sun May Arise on SMA : Newborn Screening of Spinal Muscular Atrophy in Belgium

Start date: March 5, 2018
Phase:
Study type: Observational

Medico-economic study of Newborn screening of Spinal Muscular Atrophy

NCT ID: NCT03505099 Completed - Clinical trials for Spinal Muscular Atrophy

Pre-Symptomatic Study of Intravenous Onasemnogene Abeparvovec-xioi in Spinal Muscular Atrophy (SMA) for Patients With Multiple Copies of SMN2

SPR1NT
Start date: April 2, 2018
Phase: Phase 3
Study type: Interventional

To evaluate the safety and efficacy of intravenous onasemnogene abeparvovec-xioi in pre-symptomatic patients with SMA and 2 or 3 copies SMN2

NCT ID: NCT03339830 Completed - Clinical trials for Spinal Muscular Atrophy

European Registry of Patients With Infantile-onset Spinal Muscular Atrophy

Start date: October 10, 2017
Phase:
Study type: Observational [Patient Registry]

IO-SMA-Registry is a prospective, longitudinal and observational study which objective is to collect prospectively information on longevity, psychomotor development and respiratory function of patients with infantile-onset spinal muscular atrophy.