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  • HP:0001681: Angina pectoris
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    HP:0001681: Angina pectoris

    Developed by Shray Alag, The Harker School
    Sections: Correlations, Clinical Trials, and HPO

    Correlations computed by analyzing all clinical trials.

    Navigate: Clinical Trials and HPO


    Correlated Drug Terms (5)


    Name (Synonyms) Correlation
    drug179 Ad5FGF-4 Wiki 0.71
    drug3386 Tele-medicine platform Wiki 0.71
    drug17 14C-lazertinib Wiki 0.71
    Name (Synonyms) Correlation
    drug427 BRII-198 Wiki 0.71
    drug2505 Placebo Wiki 0.03

    Correlated MeSH Terms (11)


    Name (Synonyms) Correlation
    D000787 Angina Pectoris NIH 1.00
    D060050 Angina, Stable NIH 0.71
    D003324 Coronary Artery Disease NIH 0.53
    Name (Synonyms) Correlation
    D054143 Heart Failure, Systolic NIH 0.50
    D009203 Myocardial Ischemia NIH 0.34
    D054058 Acute Coronary Syndrome NIH 0.32
    D007511 Ischemia NIH 0.29
    D003327 Coronary Disease NIH 0.27
    D006333 Heart Failure NIH 0.22
    D002318 Cardiovascular Diseases NIH 0.13
    D013577 Syndrome NIH 0.07

    Correlated HPO Terms (4)


    Name (Synonyms) Correlation
    HP:0001677 Coronary artery atherosclerosis HPO 0.58
    HP:0001658 Myocardial infarction HPO 0.38
    HP:0001635 Congestive heart failure HPO 0.24
    Name (Synonyms) Correlation
    HP:0001626 Abnormality of the cardiovascular system HPO 0.13

    Clinical Trials

    Navigate: Correlations   HPO

    There are 2 clinical trials


    1 A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multicenter, Phase 3 Study to Evaluate the Safety and Efficacy of Ad5FGF-4 in Patients With Refractory Angina Due to Myocardial Ischemia

    The purpose of this study is to determine whether a single intracoronary infusion of an adenovirus serotype 5 virus expressing the gene for human fibroblast growth factor-4 (Ad5FGF-4) is effective in improving angina-limited exercise duration, angina functional class, frequency of angina attacks, frequency of nitroglycerin usage, and quality of life. Half of the study participants will receive Ad5FGF-4, and half will receive placebo. The primary endpoint is the change from baseline to Month 6 in Exercise Tolerance Test (ETT) duration. Long-term safety of Ad5FGF-4 will also be assessed.

    NCT02928094
    Conditions
    1. Angina, Stable
    Interventions
    1. Biological: Ad5FGF-4
    2. Biological: Placebo
    MeSH:Angina Pectoris Myocardial Ischemia Coronary Artery Disease Angina, Stable Ischemia
    HPO:Angina pectoris Coronary artery atherosclerosis Myocardial infarction

    Primary Outcomes

    Description: Modified Bruce Protocol with exercise duration limited by angina or angina equivalent

    Measure: Change in Exercise Tolerance Test (ETT) duration

    Time: Baseline and Month 6

    Secondary Outcomes

    Description: Canadian Cardiovascular Society (CCS) angina classification

    Measure: Change in patient functional status (CCS class)

    Time: Baseline and Month 6

    Description: Average weekly angina episodes

    Measure: Change in weekly angina frequency

    Time: Baseline and Month 6

    Description: Average weekly nitroglycerin usage

    Measure: Change in weekly nitroglycerin usage

    Time: Baseline and Month 6

    Description: Seattle Angina Questionnaire

    Measure: Change in quality of life

    Time: Baseline and Month 6

    Description: Adverse events and clinical laboratory testing

    Measure: Safety of Ad5FGF-4

    Time: Through Month 6

    Description: Occurrence of clinically significant events

    Measure: Long-term safety of Ad5FGF-4

    Time: Through Month 60
    2 Integrated Distance Management Strategy for Patients With Cardiovascular Disease (Ischaemic Coronary Artery Disease, High Blood Pressure, Heart Failure) in the Context of the COVID-19 Pandemic

    Management of known patients with cardiovascular disease (in particular the whole spectrum of atherosclerotic ischaemic coronary artery disease, essential hypertension under treatment, and also patients with chronic heart failure under medication) and with other associated chronic pathologies, with obvious effects on the management of the pandemic with modern / distance means (e-Health) of patients at high risk of mortality in contact with coronavirus. Given the Covid-19 Pandemic, all the above complex cardiovascular patients are under the obligation to stay in the house isolated and can no longer come to standard clinical and paraclinical monitoring and control visits. Therefore, a remote management solution (tele-medicine) of these patients must be found. The Investigators endeavour is to create an electronic platform to communicate with these patients and offer solutions for their cardiovascular health issues (including psychological and religious problems due to isolation). The Investigators intend to create this platform for communicating with a patient and stratify their complaints in risk levels. A given specialist will sort and classify their needs on a scale, based on specific algorithms (derived from the clinical European Cardiovascular Guidelines), and generate specific protocols varying from 911 like emergencies to cardiological advices or psychological sessions. These could include medication changing of doses, dietary advices or exercise restrictions. Moreover, in those patients suspected of COVID infection, special assistance should be provided per protocol.

    NCT04325867
    Conditions
    1. Angina Pectoris
    2. Acute Coronary Syndrome
    3. Coronary Syndrome
    4. Coronary Artery Disease
    5. Angioplasty
    6. Stent Restenosis
    7. Hypertension
    8. Heart Failure, Systolic
    9. Depression, Anxiety
    10. Covid-19
    11. Isolation, Social
    Interventions
    1. Other: Tele-medicine platform
    MeSH:Heart Failure Cardiovascular Diseases Coronary Artery Disease Myocardial Ischemia Coronary Disease Acute Coronary Syndrome Angina Pectoris Heart Failure, Systolic Syndrome
    HPO:Abnormality of the cardiovascular system Angina pectoris Congestive heart failure Coronary artery atherosclerosis Left ventricular dysfunction Myocardial infarction Right ventricular failure

    Primary Outcomes

    Description: Development of an electronic (e-HEALTH) framework structure for management of patients with known cardiovascular disease in COVID19 pandemic social context

    Measure: Providing a special electronic platform (e-health) for remote managing cardiovascular outpatients

    Time: 6 months

    Description: patients come into direct contact with the case coordinator, who provides ongoing assistance, including for connecting to devices that ensure real-time data transmission and directing to specialist teams that establish stage diagnosis and management / therapy behavior (including adjustment). doses, decisions to discontinue medication or to add medication);

    Measure: Number of patients included in this platform

    Time: 6 months

    Secondary Outcomes

    Description: Will be the number of sessions per patient multiplied with the number of patients included

    Measure: Number of consultations/sessions given

    Time: 6 months

    HPO Nodes


    Reports

    Data processed on September 26, 2020.

    An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.

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