- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT01888770
The Effect of Prematurity and Hypertensive Disorders of Pregnancy on Offspring Cardiovascular Health (EPOCH)
연구 개요
상세 설명
While the incidence of cardiovascular disease has reduced dramatically, coinciding with favourable changes in risk factors, cardiovascular disease remains the single largest cause of mortality and premature mortality in the United Kingdom. Identification of novel biological pathways that underlie disease susceptibility raises the potential for new early primary prevention strategies to complement classical management. There is particular interest in the role of early environment in 'programming' risk of cardiovascular disease in later life and growing evidence that various early life exposures impact cardiovascular health in the longer term.
The investigators have therefore designed the EPOCH study to investigate whether those individuals born to hypertensive pregnancies and/or to a preterm birth demonstrate differences in the cardiovascular phenotype at birth, or whether they develop any differences over the first three months of life and whether this varies with other perinatal factors. This study also allows investigation of the short term impact of perinatal interventions used in this cohort. Comprehensive multi-modality non-invasive imaging measures of cardiovascular structure and function allow precise quantification of cardiovascular phenotype in this population.
연구 유형
등록 (예상)
연락처 및 위치
연구 장소
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Oxfordshire
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Oxford, Oxfordshire, 영국, OX3 9DU
- 모병
- Cardiovascular Clinical Research Facility, Dept of Cardiovascular Medicine, University of Oxford
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연락하다:
- Paul Leeson, PhD, MRCP
- 이메일: paul.leeson@cardiov.ox.ac.uk
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수석 연구원:
- Paul Leeson, PhD, FRCP
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
샘플링 방법
연구 인구
설명
Inclusion Criteria:
- Available for assessment within the neonatal period,
- Parent is willing and able to give informed consent for participation in the study,
- Physical condition is suitable to allow non-invasive vascular testing,
- Mother meets criteria for inclusion in the study and is willing to participate in the study. (Aged >/= 16 years and Is able and willing to give informed consent for participation in the study, and is able and willing to give informed consent for her infants participation in the study. )
- Cases: Diagnosed during pregnancy with preeclampsia or gestational hypertension and/or delivered preterm (<37 weeks gestation)
- Controls: No history of gestational hypertension or preeclampsia during this pregnancy and delivered at term (>37 weeks gestation)
Exclusion Criteria:
- Parent is unwilling to give consent,
- Unavailable for assessment of cardiovascular system,
- Physical condition unsuitable to allow for non-invasive testing of cardiovascular system,
- Evidence of congenital cardiovascular disease (with the exception of Persistent Patent Ductus Arterious (PDA) and Atrial Septal Defect (ASD)),
- Cardiorespiratory instability at time of proposed measures,
- Active infection at time of proposed study measures,
- Mother of infant is excluded from the study. (Aged <16 years, unable or unwilling to consent to study or Physical condition post delivery such that it would preclude participation in the study)
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
코호트 및 개입
그룹/코호트 |
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Normotensive Term
Infants born at term (>37 weeks) to Normotensive pregnancies
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Term Preeclampsia
Infants born at term (>37 weeks gestation) and exposed to a preeclamptic pregnancy
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Preterm Normotensive
Infants born to Normotensive pregnancies at <37 weeks gestation
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Preterm Hypertensive
Infants born to hypertensive pregnancies at <37 weeks completed gestation
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Term Pregnancy-induced Hypertension
Infants born at term (>37 weeks gestation) and exposed to pregnancy-induced hypertension
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Systolic Cardiac Function
기간: Birth and 3 months
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Cardiac Function will be assessed by ECHO at birth and 3 months
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Birth and 3 months
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Micro-vascular Structure
기간: Birth and 3 months
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Micro-vascular Structure will be assessed using Side Stream Dark Field (SDF) imaging device at birth and 3 months (as capillary density at baseline)
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Birth and 3 months
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Pulse wave velocity and pulse-wave analysis
기간: Birth and 3 months
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Birth and 3 months
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Cardiac Structure
기간: Birth and 3 months
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Cardiac structure will be assessed by echocardiography at in utero, at birth and 3 months (as left and right ventricular mass)
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Birth and 3 months
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Cardiac diastolic function
기간: Birth and 3 months
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Cardiac Function will be assessed by ECHO at birth and 3 months
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Birth and 3 months
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Blood pressure
기간: Birth and 3 months
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Birth and 3 months
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Heart rate variability
기간: Birth and 3 months
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Heart rate variability will be assessed by a 5 minute electrocardiogram
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Birth and 3 months
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공동 작업자 및 조사자
수사관
- 수석 연구원: Paul Leeson, PhD, FRCP, University of Oxford Department of Cardiovascular Medicine
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (예상)
연구 완료 (예상)
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 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. .