- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT01226641
Usefulness of a Telemedicine System for OSA Patients Follow-up With High Cardiovascular Risk (TELESAS)
연구 개요
상세 설명
The obstructive sleep apnea syndrome (OSAS) corresponds to repeated epochs of complete or incomplete pharynx collapses occurring during sleep. The Continuous Positive Airway Pressure is the gold standard treatment for OSAS. It consists of air insufflation in upper airways with a pressure of about 5 to 15 cm of water with a facial or nasal mask. CPAP treatment reduces cardiovascular morbi-mortality.
OSAS is associated with cardiovascular mortality. A dose response effect exists between severity and arterial blood pressure. A recent meta-analysis has shown in unselected OSAS patients with or without hypertension, treated or non-treated for hypertension, CPAP reduces 24 h ambulatory blood pressure of approximately 2 mmHg. This decrease corresponds to a significant reduction in cardiovascular risk.
The aim of the present study is to include OSAS patients with a high cardiovascular risk and to measure the effect of CPAP on home measurements of arterial blood pressure. This controlled randomized trial will compare the effect CPAP on arterial blood pressure in a group with a telemedicine system versus a group with standard home care CPAP treatment.
An interim analysis will be carried out when 100 patients have been included in the study.
연구 유형
등록 (실제)
단계
- 해당 없음
연락처 및 위치
연구 장소
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Boulogne Billancourt, 프랑스, 92100
- Liberal Office
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Brest, 프랑스, 29200
- Clermont Tonerre military hospital
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Chambery, 프랑스, 73000
- Liberal Office
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Grenoble, 프랑스, 38000
- University Hospital
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Grenoble, 프랑스, 38000
- Liberal Office
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Montigny les Metz, 프랑스, 57950
- Liberal Office
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Nancy, 프랑스, 54000
- Liberal Office
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Quimper, 프랑스, 29107
- Cornouaille Hospital
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St Andre les Vergers, 프랑스, 10120
- Montier Polyclinic
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St Avold, 프랑스, 57500
- Hospitalor Hospital
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St Jean de Maurienne, 프랑스, 73300
- Liberal Office
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St Martin les Boulogne, 프랑스, 62280
- Liberal Office
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StIsmier, 프랑스, 38330
- Liberal Office
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Strasbourg, 프랑스, 67000
- Liberal Office
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- 18 to 85 years old men and women
- stable patient
- BMI<40kg/m²
- OSA patients diagnosed with polysomnography or polygraphy
- SCORE>5% and/or cardiovascular disease pas history :
- transient ischemic attack, stroke, cerebral haemorrhagy
- myocardial infraction, angor, coronary revascularization, arteriopathy, aortic aneurism
Exclusion Criteria:
- central sleep apnea syndrome
- SCORE<5%
- cardiac failure
- past history of hypercapnic chronic respiratory failure
- past history of severe or intercurrent pathology which can not allow the patient follow-up
- Incapacitated patients in accordance with article L 1121-6 of the public health code
- patients taking part in another clinical trial
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
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실험적: Telemedecine
CPAP treatment with telemedicine system
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CPAP treatment with telemedicine system
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활성 비교기: Standard Care
Standard care, including CPAP
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Standard care, including CPAP
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Home Arterial Blood Pressure
기간: Home arterial Blood Pressure is assessed at week 1
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the primary outcome is assessed at weeks 1 and 16 for the both groups, moreover home arterial blood pressure is assessed each day, 2 times : morning and afternoon in the telemedicine group.
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Home arterial Blood Pressure is assessed at week 1
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Home Arterial Blood Pressure
기간: Home arterial Blood Pressure is assessed at week 16
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the primary outcome is assessed at weeks 1 and 16 for the both groups, moreover home arterial blood pressure is assessed each day, 2 times : morning and afternoon in the telemedicine group.
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Home arterial Blood Pressure is assessed at week 16
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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CPAP compliance
기간: week 16
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the CPAP compliance is assessed in the two groups at week 16
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week 16
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Sleepiness
기간: weeks 1 and 16
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Sleepiness is assessed with Epworth Sleepiness Scale at weeks 1 and 16 for the two groups
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weeks 1 and 16
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Physical Activity
기간: week 1
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Daily Physical Activity is assessed with an accelerometer (Sensewear Armband, Bodymedia) at weeks 1 and 16 in the two groups.
Daily expenditure, steps number, daily METs are assessed.
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week 1
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Quality of Life
기간: week 16
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Quality of life is assessed with SF-12 questionnaire at weeks 1 and 16 in the two groups.
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week 16
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Cardiovascular risk SCORE
기간: Week 1
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The cardiovascular risk SCORE is assessed at weeks 1 and 16 in the two groups.
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Week 1
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Sleepiness
기간: week 16
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Sleepiness is assessed with Epworth Sleepiness Scale at weeks 1 and 16 for the two groups
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week 16
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Physical Activity
기간: week 16
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Daily Physical Activity is assessed with an accelerometer (Sensewear Armband, Bodymedia) at weeks 1 and 16 in the two groups.
Daily expenditure, steps number, daily METs are assessed.
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week 16
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Quality of Life
기간: week 1
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Quality of life is assessed with SF-12 questionnaire at weeks 1 and 16 in the two groups.
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week 1
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Cardiovascular risk SCORE
기간: Week 16
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The cardiovascular risk SCORE is assessed at weeks 1 and 16 in the two groups.
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Week 16
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공동 작업자 및 조사자
수사관
- 수석 연구원: Jean Louis PEPIN, Prof, PhD, University Hospital, Grenoble
간행물 및 유용한 링크
일반 간행물
- Mendelson M, Vivodtzev I, Tamisier R, Laplaud D, Dias-Domingos S, Baguet JP, Moreau L, Koltes C, Chavez L, De Lamberterie G, Herengt F, Levy P, Flore P, Pepin JL. CPAP treatment supported by telemedicine does not improve blood pressure in high cardiovascular risk OSA patients: a randomized, controlled trial. Sleep. 2014 Nov 1;37(11):1863-70. doi: 10.5665/sleep.4186.
- Mendelson M, Tamisier R, Laplaud D, Dias-Domingos S, Baguet JP, Moreau L, Koltes C, Chavez L, de Lamberterie G, Herengt F, Levy P, Flore P, Pepin JL. Low physical activity is a determinant for elevated blood pressure in high cardiovascular risk obstructive sleep apnea. Respir Care. 2014 Aug;59(8):1218-27. doi: 10.4187/respcare.02948.
연구 기록 날짜
연구 주요 날짜
연구 시작
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 (추정)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- InitiativePS-TELESAS
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. .
폐쇄성 수면 무호흡 증후군에 대한 임상 시험
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Fujian Shengdi Pharmaceutical Co., Ltd.모병Bstructive sleep apnea (OSA) 및 비만중국