- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02235090
Study of Feasibility to Reliably Measure Functional Abilities' Changes in Nonambulant Neuromuscular Patients Without Trial Site Visiting
Assessment of Feasibility and Statistical Reliability of Functional Outcomes Measurement in Neuromuscular Patients Without Trial Site Visiting by Standard Functional Scales and by Special Autonomic Device in Double-blind, Placebo Controlled Study of Cervical Spinal Cord Transdermal Direct Current Stimulation in Patients With Spinal Muscular Atrophy
Clinical trials organization in several neuromuscular disorders (NMD) has some specific issues. Nonambulant status and difficulties with transportation are among them. Moreover a lot of patients with NMD have so poor condition that even short transportation is able to worse it. Such situation forces researchers to limit a region of recruitment for clinical trials and to exclude from trials more severe subgroup of patients, which cause additional issues especially for rare diseases.
The purpose of this study is to prove hypothesis about possibility to reliably monitor patient condition remotely, without trial site visiting. Visit-free study design is potentially able to widen eligible patient population and to decrease patient dropout rate as well as burden of numerous assessments. Meanwhile assessment frequency could be increased enabling monitoring of short fluctuations in patients' condition.
Spinal muscular atrophy (SMA) is a rare neuromuscular condition to which all mentioned above issues are completely applicable. Direct current stimulation (DCS) of neural structures is well studied and safe intervention, however, its effects on SMA patients' strength and durability has not been reported for today. The investigators suppose that investigation of DCS action in SMA patient population is an adequate model for visit-free design feasibility, reliability and sensitivity evaluation.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Kharkiv, Ukraine, 61068
- SI "Institute of Neurology, Psychiatry and Narcology of NAMS of Ukraine"
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Signed informed consent
- 5q SMA confirmed by molecular testing
Exclusion Criteria:
- Need for ventilation
- Hypersensitivity (pain or allergic reaction) to current stimulation
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Andet
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Sham-komparator: Zero-strength of direct current stimulation
Sham transdermal direct current stimulation of cervical spinal cord
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10 minutes direct current stimulation of 0, 100 microamperes, 1 milliampere strengths applied through dermal electrodes to cervical spinal cord
|
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Eksperimentel: 100 microamperes direct current stimulation
Transdermal direct current stimulation of cervical spinal cord
|
10 minutes direct current stimulation of 0, 100 microamperes, 1 milliampere strengths applied through dermal electrodes to cervical spinal cord
|
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Eksperimentel: 1 milliampere direct current stimulation
Transdermal direct current stimulation of cervical spinal cord
|
10 minutes direct current stimulation of 0, 100 microamperes, 1 milliampere strengths applied through dermal electrodes to cervical spinal cord
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Strength Changes from baseline measured by handheld myometry after spinal cord direct current stimulation of different intensity
Tidsramme: Before and 0, 15, 30 minutes after spinal cord direct current stimulation
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Before and 0, 15, 30 minutes after spinal cord direct current stimulation
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Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Short time fluctuations of Hammersmith Functional Motor Scale indexes
Tidsramme: Three times, three days consecutive measurement, every two months, assessed up to 6 months
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Three times, three days consecutive measurement, every two months, assessed up to 6 months
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Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: Andriy V. Shatillo, MD, PhD, State Institution "Institute of Neurology, Psychiatry and Narcology of NAMS of Ukraine"
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- CSMA-INPN-1
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