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55 Resultados de la búsqueda.
Relevancia Evaluación Nuevo primero Antiguo primero

Endpoint Myocardial infarction GSK study Chronic Coronary Heart Disease NCT00799903

- 3/1/18 - 1 formulario, 3 itemgroups, 48 items, 1 idioma
Itemgroups: Investigator Section, CEC Section, CEC STATUS
Study ID: 100601 Clinical Study ID: LPL100601 Study Title: LPL100601, A Clinical Outcomes Study of Darapladib versus Placebo in Subjects with Chronic Coronary Heart Disease to Compare the Incidence of Major Adverse Cardiovascular Events (MACE) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00799903 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: darapladib Trade Name: darapladib Study Indication: Atherosclerosis Study part: Endpoint Myocardial infarction - Repeating form (Scheduled visits)

Eligibility Myocardial Infarction NCT00850473

- 14/8/17 - 1 formulario, 2 itemgroups, 13 items, 1 idioma
Itemgroups: Inclusion Criteria, Exclusion Criteria
PET/CT Study in the Diagnosis of Coronary Plaque; ODM derived from: https://clinicaltrials.gov/show/NCT00850473

Eligibility Myocardial Infarction NCT00324766

- 15/5/17 - 1 formulario, 2 itemgroups, 16 items, 1 idioma
Itemgroups: Inclusion Criteria, Exclusion Criteria
Levosimendan in Acute Heart Failure Following Acute Myocardial Infarction.; ODM derived from: https://clinicaltrials.gov/show/NCT00324766

Myocardial Infarction Report Form PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

- 3/4/17 - 1 formulario, 7 itemgroups, 24 items, 1 idioma
Itemgroups: Myocardial Infarction Report Form, Assessments, Details for myocardial infarction, Hospitalization, Fatal Outcome, Please remember to fax Supporting Documentation clearly identified with the patient number, Invenstigator´s Declaration
The purpose of the trial is to determine if extended-release dipyridamole + aspirin [Aggrenox, Asasa ntin] is superior to clopidogrel [Plavix], and if telmisartan [Micardis, Gliosartan, Kinzal, Kinzalm ono, Predxal, Pritor, Samertan, Telmisartan] is superior to placebo, in the presence of background antihypertensive therapy, in prevention of a second stroke in patients who have recently suffered a stroke and therefore are at high risk of suffering another one. Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT00153062?term=NCT00153062&rank=1

Eligibility Myocardial Infarction NCT00060554

- 30/10/16 - 1 formulario, 2 itemgroups, 12 items, 1 idioma
Itemgroups: Inclusion Criteria, Exclusion Criteria
A Safety and Efficacy Trial Evaluating the Use of Fondaparinux in Percutaneous Coronary Intervention (PCI)(63133)(WITHDRAWN); ODM derived from: https://clinicaltrials.gov/show/NCT00060554

Input Data Elements CDSS Acute Coronary Syndrome or Myocardial Infarction Management Strauss 2014

- 13/10/16 - 1 formulario, 1 itemgroup, 9 items, 1 idioma
Itemgroup: Risk assessment criteria
Input Data Elements CDSS for Acute Coronary Syndrome or Myocardial Infarction Management to evaluate impact of a real-time decision support to guide percutaneous PCI bleeding avoidance strategies. Published by Strauss et al. 2014

Input Data Elements CDSS Acute Coronary Syndrome or Myocardial Infarction Management Milani 2012

- 10/10/16 - 1 formulario, 1 itemgroup, 5 items, 1 idioma
Itemgroup: Risk factors
Input Data Elements CDSS for Acute Coronary Syndrome or Myocardial Infarction Management to evaluate computer assisted decision support enhancing the likelihood of perfect care in acute coronary syndrome. Published by Milani et al. 2012

AAFP: Acute Myocardial Infarction Admission Order

- 26/6/16 - 1 formulario, 12 itemgroups, 56 items, 2 idiomas
Itemgroups: Default Itemgroup, Status, Attending, Admitting Diagnosis, Condition, Allergies, Diet, Activity, Nursing, Medications, Lab, Consider
AAFP: Acute Myocardial Infarction Admission Order , Standardizes Admission Orders, Author: Robert M. Wiprud, MD The primary purpose of these Ordersets is to decrease unnecessary variability and to improve quality through standardized Admission Orders. Developed by the Scott & White Clinic at College Station, Texas. Copyright © 2006 American Academy of Family Physicians. Physicians may photocopy or adapt for use in their own practices; all other rights reserved. Wiprud RM. Providing consistent care with standardized admission orders. Fam Pract Manag. September 2006: 49-52 See http://www.aafp.org/fpm/2006/0900/p49.html This ODM Form includes the second section ("Acute Myocardial Infarction Admission Order").

Myocardial Infarction Protocol PhenX Toolkit

- 26/4/16 - 1 formulario, 1 itemgroup, 18 items, 1 idioma
Itemgroup: PhenX - myocardial infarct protocol
This measure assesses if an individual has had a myocardial infarction (MI) through collection of personal history of disease, treatment and procedure histories, and medical record abstraction. ODM derived from: https://cde.nlm.nih.gov Primary source: https://www.phenxtoolkit.org/ Recent publication: Hendershot, T., Pan, H., Haines, J., Harlan, W.R., Marazita, M.L., McCarty, C.A., Ramos, E.M., and Hamilton, C.M. (2015) Using the PhenX toolkit to add standard measures to a study. Curr. Protoc. Hum. Genet. 86:1.21.1-1.21.17. doi: 10.1002/0471142905.hg0121s86 Permission to publish granted by Carol M. Hamilton.

Outcome event myocardial infarction Coronary Artery Bypass graft surgery in patients with Asymptomatic Carotid Stenosis DRKS00000521 - CABACS Case Report Form [Outcome event myocardial infarction]

- 7/3/16 - 1 formulario, 1 itemgroup, 17 items, 1 idioma
Itemgroup: Endpoint event "myocardial infarction"
Coronary Artery Bypass graft surgery in patients with Asymptomatic Carotid Stenosis. A randomized controlled clinical trial. Short title: "CABACS" DRKS Number:DRKS00000521 IRSCTN Number:ISRCTN13486906 Phase:Therapeutic confirmatory(Phase III) Head of clinical trial: Prof. Dr. med. Christian Weimar University Duisburg-Essen Phone: 0201/723-6503 Fax: 0201/723-6948 e-mail: christian.weimar@uk-essen.de University Hospital Essen Hospital for Neurology Hufelandstr. 55 45122 Essen Trial coordinator: Dr. med. Stephan Knipp Phone: 0201/723-4915 Fax: 0201/723-5451 e-mail: stephan.knipp@uk-essen.de University Duisburg-Essen University Hospital Essen Hospital for thoracic- and cardiovascular surgery Hufelandstr. 55 45122 Essen Data Management: Anja Marr Phone: 0201/92239-257 Fax: 0201/92239-333 o. 0201/723-5933 e-mail: anja.marr@uk-essen.de University Hospital Essen Center for clinical trials Essen c/o IMIBE Hufelandstr. 55 45122 Essen Monitoring: Dipl.-Biol. Konstantinos Bilbilis Phone: 0201/92239-252 Fax: 0201/92239-310 e-mail: konstantinos.bilbilis@uk-essen.de University Hospital Essen Center for clinical trials Essen c/o IMIBE Hufelandstr. 55 45122 Essen

Eligibility Coronary Disease NCT01422317

- 24/1/16 - 1 formulario, 2 itemgroups, 11 items, 1 idioma
Itemgroups: Inclusion Criteria, Exclusion Criteria
Effects of High-dose n-3 Fatty Acids on Clinical Outcome and Serum Lipids - Omacor Following Acute Myocardial Infarction; ODM derived from: https://clinicaltrials.gov/show/NCT01422317

Global registry of acute coronary events (GRACE) - GRACE Initial Form v3.5

- 25/11/15 - 1 formulario, 17 itemgroups, 193 items, 1 idioma
Itemgroups: General information, Enrollment, Demographics, Medical History, Presentation, ECG Findings, Laboratory, Procedures, Cardiac Cath/Interventions, LVEF, Thrombolytics, Antiplatelets/Antithrombins/Anticoagulants, Other Medications, Medication Contraindications, Lifestyle interventions, In-hospital Events: After Presentation, Discharge status
GRACE is an international observational database of outcomes for patients who are hospitalized with an acute coronary syndrome (ACS). GRACE includes over 200 hospitals in 28 countries that enroll a total of more than 10,000 patients per year. Participating physicians receive confidential quarterly reports showing ther outcomes side-by-side with the aggregate outcomes of all participating hospitals. (http://www.outcomes-umassmed.org/GRACE/overview.aspx)

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