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Modelos de datos seleccionados

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

Multiple Sclerosis - Patient Questionnaire (REGIMS)

- 9/12/14 - 1 formulario, 15 itemgroups, 119 items, 2 idiomas
Itemgroups: General information, First Symptoms, Diagnostic procedure within the past 12 months, Fatigability Multiple Sclerosis, Course, Aid, manufactured, Medical benefits, Medical benefits past 12 months, Treatment satisfaction, Family history, Symptoms within past 12 months, Medication within last 7 days, Demographics, Doctor visit, Quality of life
Patientenfragebogen Multiple Sklerose REGIMS http://epi.uni-muenster.de

Registry for Sickle Cell Diseases, 1.registration form - Sichel-Reg, 1. Meldebogen

- 17/9/21 - 1 formulario, 7 itemgroups, 38 items, 2 idiomas
Itemgroups: Patient data, Treating Clinic, General practitioner, Patient Characteristics, Professional career, Comments, Signature
Registerzentrale: Dr. Dickerhoff / Dr. Potthoff, Klinik für Kinder-Onkologie, -Hämatologie und Klinische Immunologie, Universitätsklinikum Düsseldorf

REGIMS - SUE Report

- 27/9/21 - 1 formulario, 10 itemgroups, 43 items, 2 idiomas
Itemgroups: SUE, Patientenangaben, SUE: Beschreibung, SUE: Behandlung, SUE: Ausgang, SUE: MS-Medikation, SUE: Begleitmedikation, SUE: Relevante Vorerkrankung / Sypmtome, Ergebnisse der relevanten Diagnostischen Untersuchungen, Kontaktdaten des Berichterstatters
Schwerwiegendes unerwünschtes Ereignis (SUE) in der Therapie SUE Berichtsformular Bitte ausfüllen und faxen oder senden an: Westfälische Wilhelms-Universität Münster, Institut für Epidemiologie und Sozialmedizin, Albert-Schweitzer-Campus 1, Gebäude 03, 48149 Münster Fax: (0251) 83-55300, E-Mail: regims@uni-muenster.de http://epi.uni-muenster.de

Multiple Sclerosis - Base Sheet (REGIMS)

- 19/1/15 - 1 formulario, 9 itemgroups, 38 items, 2 idiomas
Itemgroups: General information, Disease-specific information, Current Symptoms Multiple Sclerosis, Past treatment Multiple Sclerosis, Current Therapy Multiple Sclerosis, Cortisone, MRT, Disease history, Pregnancy, current
Medizinischer Basisbogen Multiple Sklerose http://epi.uni-muenster.de

Multiple Sclerosis - In-/Exclusion Criteria (REGIMS)

- 12/12/14 - 1 formulario, 3 itemgroups, 8 items, 2 idiomas
Itemgroups: Inclusion criteria, Exclusion criteria, Comments
REGIMS Multiple Sklerose-Register http://epi.uni-muenster.de

eurILDreg - K-BILD Questionnaire

- 14/8/24 - 32 formularios, 2 itemgroups, 16 items, 1 idioma
Itemgroups: <div class="rich-text-field-label"><p>KING'S BRIEF INTERSTITIAL LUNG DISEASE QUESTIONNAIRE (K-BILD)</p> <p>Please answer the following questions as precise as possible:</p> <p>&nbsp;</p></div>, K-BILD Questionnaire
This file contains the metadata, events, and data for REDCap project "eurILDreg".

Leicester Cough Questionnaire

2 itemgroups 20 items

MDT board diagnosis

3 itemgroups 70 items

Supportive therapy and immunisation

4 itemgroups 14 items

Health care utilization

3 itemgroups 159 items

Clinical diagnosis

2 itemgroups 67 items

Symptom survey

1 itemgroup 8 items

DZG-Basisdatensatz - DZG_Core_Dataset

- 12/7/24 - 1 formulario, 2 itemgroups, 28 items, 2 idiomas
Itemgroups: General_Information, Diseases
Deutsch: Die Deutsche Zentren der Gesundheitsforschung (DZG) haben sich dazu verpflichtet, die Standardisierung und Harmonisierung ihrer Daten und Prozesse voranzutreiben, um die Zusammenarbeit und Forschungskapazitäten zu stärken. In diesem Zusammenhang wurde der DZG Basisdatensatz von klinisch Forschendern aller DZG entwickelt, der prospektiv in DZG geförderten Studien zu erheben ist. Der DZG-übergreifende Basisdatensatz ermöglicht es Forschenden, mit den erhobenen Daten in offenen Projekten zu arbeiten und trägt so zur Stärkung der Forschungskapazitäten bei. English: The German Centers for Health Research (DZG) have committed to advancing the standardization and harmonization of their data and processes to strengthen collaboration and research capabilities. In this context, the DZG core dataset was developed by clinical researchers from all DZG, which is to be collected prospectively in DZG-funded studies. The DZG basic dataset allows researchers to work with the collected data in open projects and thus contributes to strengthening research capacities.

Heidelberger Register chronischer Singultus - Primary Visit

- 22/3/22 - 2 formularios, 8 itemgroups, 118 items, 2 idiomas
Itemgroups: Demografie und Anamnese bei der Visite, Durchgeführte Diagnostik, Ausführung der Komorbiditäten, Aktuelle Medikation, Pausierung der Medikation, Befund und Beurteilung, Quantifizierung der Symptome, Empfehlungen
Erhebung eines klinischen Datensatzes zum chronischen Singultus (Schluckauf). Durchgeführt durch die Sektion Schmerzmedizin an der Klinik für Anästhesiologie und Intensivmedizin am Universtätsklinikum Heidelberg. Dr. med. Claudia Busch & PD Dr. Jens Keßler

Secondary Visit

6 itemgroups 84 items

Heidelberg Perioperative Deep Data Study – a prospective cohort study - PDMS ICU - Primary data

- 10/1/22 - 1 formulario, 8 itemgroups, 125 items, 1 idioma
Itemgroups: Respiratory system data, Cardiovascular system data, Diagnosis related data, Laboratory values, Medication related data, Medical Scores, Medical device related data, Quantitative data body fluids
HeiPoDD registry will form a clinical database and a corresponding biobank as the basis to predict overall postoperative morbidity and mortality using data-driven, personalized risk prediction from the entirety of available clinical records. Prospective single-center observational registry. DRKS00025924

Heidelberg Perioperative Deep Data Study – a prospective cohort study - DRKS00025924 - Patient monitoring - primary data

- 28/12/21 - 1 formulario, 9 itemgroups, 242 items, 1 idioma
Itemgroups: Height Weight BSA, Respiratory system data, Laboratory data, Medication data, Neurological data, Clinical Scores, Temperature data, Electrocardiography data, Cardiovascular system data
HeiPoDD registry will form a clinical database and a corresponding biobank as the basis to predict overall postoperative morbidity and mortality using data-driven, personalized risk prediction from the entirety of available clinical records. Prospective single-center observational registry. DRKS00025924

ACTION Registry®-GWTG™ - ACTION Registry

- 18/11/21 - 1 formulario, 8 itemgroups, 186 items, 1 idioma
Itemgroups: Demographics, Admission, Cardiac status on first medical contact, History and Risk Factors, Medications, Procedures and Tests, Reperfusion Strategy, In-Hospital clinical events
The ACTION Registry®–GWTG™ is a risk-adjusted, outcomes-based quality improvement program that focuses exclusively on high-risk STEMI/NSTEMI patients. It helps hospitals apply ACC/AHA clinical guideline recommendations in their facilities and provides invaluable tools to measure care and achieve quality improvement goals. (http://cvquality.acc.org/NCDR-Home/Registries/Hospital-Registries.aspx)

Cell Therapy Registry EBMT

- 27/9/21 - 1 formulario, 13 itemgroups, 74 items, 1 idioma
Itemgroups: Cell Therapy Registry – Med-A, CENTRE IDENTIFICATION, REPORT INFORMATION, PATIENT IDENTIFICATION, INDICATION FOR TREATMENT If Primary disease, CELL THERAPY TREATMENT, GRAFT MANIPULATION, TREATMENT, RESPONSE, DATE OF LAST CONTACT, CENTRE IDENTIFICATION, REPORT INFORMATION, PATIENT IDENTIFICATION
The Cell Therapy Registry (CTR) aims to collect data on fetal or adult stem cells, or progenitor cells used for treatment other than haematopoietic stem cell transplantation or donor lymphocyte infusion, as well as data on the clinical characteristics and outcome of the patients. Data will be collected on characteristics of the cell graft, /in/ or /ex vivo/ cell manipulation and the cell origin (autologous versus allogeneic). Data will include details on patients treated with mesenchymal cells, for instance, to enhance haematopoietic engraftment, for prophylaxis and treatment of GvHD. The registry will also include data on patients treated by other disciplines for neurologic, rheumatologic, cardiac and inflammatory bowel diseases and tissue regeneration. For further information, please contact: The registry will also include data on patients treated by other disciplines for neurologic, rheumatologic, cardiac and inflammatory bowel diseases and tissue regeneration. For further information, please contact: Dr. Katarina Le Blanc Karolinska University Hospital Centre for Allogeneic Stem Cell Transplantation Huddinge SE-141 86 Stockholm Sweden e-mail : Katarina.Leblanc@ki.se please refer: http://www.ebmt.org/Contents/Data-Management/Registrystructure/MED-ABdatacollectionforms/Pages/MED-AB-data-collection-forms.aspx

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