- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 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.
연구 개요
연구 유형
단계
- 해당 없음
연락처 및 위치
연구 장소
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Kharkiv, 우크라이나, 61068
- SI "Institute of Neurology, Psychiatry and Narcology of NAMS of Ukraine"
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Signed informed consent
- 5q SMA confirmed by molecular testing
Exclusion Criteria:
- Need for ventilation
- Hypersensitivity (pain or allergic reaction) to current stimulation
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 다른
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 네 배로
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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가짜 비교기: 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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실험적: 100 microamperes direct current stimulation
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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실험적: 1 milliampere direct current stimulation
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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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
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Strength Changes from baseline measured by handheld myometry after spinal cord direct current stimulation of different intensity
기간: 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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2차 결과 측정
결과 측정 |
기간 |
|---|---|
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Short time fluctuations of Hammersmith Functional Motor Scale indexes
기간: 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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공동 작업자 및 조사자
수사관
- 수석 연구원: Andriy V. Shatillo, MD, PhD, State Institution "Institute of Neurology, Psychiatry and Narcology of NAMS of Ukraine"
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .