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临床试验/NCT05980728
NCT05980728尚未招募不适用

The Prognostic Value of Biomarker in Connective Tissue Disease Patients With Pulmonary Hypertension

The First Affiliated Hospital with Nanjing Medical University0 个研究点目标入组 500 人开始时间: 2023年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
500
主要终点
Death

研究概览

简要总结

Adult patients with suspected or confirmed Connective Tissue Disease Patients (CTD)With Pulmonary Hypertension(PH)will be recruited. Patients will be approached, consented, have baseline demographics, diagnostics and disease activity measures recorded, and blood taken. The collection of data and biological material will mirror usual clinical practice as far as possible. Subjects will ideally attend further visits at 3, 6 and 12 months to have bloods taken, outcome measures recorded and questionnaires completed.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Definite diagnosis of CTD included Systemic lupus erythematosus(SLE) diagnosed according to the 2019 The European Alliance of Associations for Rheumatology(EULAR) criteria, primary Sjogren's syndrome (pSS) defined according to the 2016 American College of Rheumatology(ACR) criteria, Systemic Sclerosis(SSc) defined according to the 2013 ACR criteria, mixed connective tissue disease (MCTD) defined by Sharp criteria, and Rheumatoid Arthritis(RA) defined according 2010 ACR criteria of two or more CTD at the same time were defined as having overlap syndrome (OS). Patients who had clinical and serological manifestations suggestive of systemic autoimmune diseases but did not fulfil the classification criteria for CTD were defined as having undifferentiated CTD (UCTD).
  • PAH was diagnosed by right heart catheterization was defined as mean Pulmonary Artery Pressure (mPAP)>20 Millimeters of mercury(mmHg), Pulmonary Artery Wedge Pressure(PAWP)≤15mmHg, Pulmonary Vascular Resistance(PVR)>2 Wood

排除标准

  • significant interstitial lung disease or chronic obstructive pulmonary disease;
  • left heart disease or congenital heart disease associated with pulmonary hypertension;
  • chronic thromboembolic pulmonary hypertension;
  • portal hypertension;
  • drug or toxin exposure;
  • HIV infection;
  • any other diseases known to be associated with PAH;
  • age<18 years.

结局指标

主要结局

Death

时间窗: 30 years

number of participants with All cause death

次要结局

  • Clinical worsening(30 years)

研究者

申办方类型
Other
责任方
Sponsor

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