Reset filter
Keywords
Medical History Taking ×
Show more Keywords
Table of contents
  1. 1. Clinical Trial
  2. 2. Routine Documentation
  3. 3. Registry/Cohort Study
  4. 4. Quality Assurance
  5. 5. Data Standard
  6. 6. Patient-Reported Outcome
  7. 7. Medical Specialty
Selected data models

You must log in to select data models for download or further analysis.

647 Search results.
Relevance Rating New first Old first

Common Data Elements for Retinal Neovascular Diseases - Risk Factors or Past Medical History

- 9/20/21 - 4 forms, 1 itemgroup, 35 items, 2 languages
Itemgroup: Risk Factors; Past Medical History
Common Data Elements for retinal neovascular diseases. The CDEs may be used in clinical routine, clinical trial, patient outcome, quality assurance and registry documentation of Age related macular degeneration (AMD), Diabetic Retinopathy (DR) and Retinal vein occlusion (RVO). The CDEs were developed by the Institute of Medical Informatics of the University Muenster in cooperation with the Department of Ophthalmology of the University Hospital Muenster.

Diagnosis and Examination

1 itemgroup 11 items

Eye Examination

1 itemgroup 18 items

Therapy

1 itemgroup 9 items

Hypersensitivity/ Anaphylaxis Evaluation Mepolizumab HES NCT00086658 - Hypersensitivity/ Anaphylaxis Evaluation

- 9/20/21 - 1 form, 1 itemgroup, 53 items, 1 language
Itemgroup: evaluation Hypersensitivity
Study part: Hypersensitivity/ Anaphylaxis Evaluation.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

EUMDS registry DRKS00003844 NCT00600860 - Patient registration

- 9/20/21 - 9 forms, 1 itemgroup, 12 items, 1 language
Itemgroup: Patient registration
Further Information: http://www.eumds.org/

Eligibility

1 itemgroup 5 items

Visit details

6 itemgroups 29 items

Bone marrow assessment

3 itemgroups 13 items

Concomitant treatment

1 itemgroup 5 items

Withdrawal

2 itemgroups 7 items

General medical history

1 itemgroup 5 items

Family prevalence (EHR archetype) - openEHR-EHR-CLUSTER.family_prevalence.v1

- 9/20/21 - 1 form, 1 itemgroup, 10 items, 1 language
Itemgroup: openEHR-EHR-CLUSTER.family_prevalence.v1.xml
Derived from www.openehr.org Use to record information about the prevalence of an identified risk factor, problem or diagnosis in genetic and non-genetic family members. This archetype has specifically been designed to be used in the 'Detail' SLOT within the EVALUATION.health_risk archetype to support assessment of risk in the subject of care for the identified 'Risk factor' and the 'Family prevalence' SLOT in the EVALUATION.family_history archetype. It can also be used in the 'Specific details' SLOT within the EVALUATION.problem_diagnosis archetype ,or other EVALUATION or CLUSTER archetypes, where clinically appropriate.

Dose Level 1 GSK Ropinirole Restless Legs Syndrome 101468

- 9/20/21 - 1 form, 11 itemgroups, 67 items, 1 language
Itemgroups: Patient Information, Predose Checklist, RLS Rating Scale, Prior Medication, Pregnancy Test, Pre-Dose Vital Signs, Baseline Signs and Symptoms, Dosing Details, Post-Dose Vital Signs, Adverse Event, Study Protocol
Study ID: 101468/207 Clinical Study ID: SKF-101468/207 Study Title:A double-blind, randomized, placebo-controlled, parallel-group study to investigate the tolerability of a dose-escalating regimen of ropinirole in patients suffering from Restless Legs Syndrome (RLS). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 2 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication : Restless Legs Syndrome Dose Level 1 (Day 1)

Pediatric medical history MS University Hospital Muenster (UKM) Subform - Pädiatrische Anamnese MS University Hospital Muenster (UKM) Subform

- 9/20/21 - 1 form, 10 itemgroups, 80 items, 1 language
Itemgroups: General information, Current medical history, Medical history, Peripartum history, Milestones, Prior hospital admission and surgery, Family social history, Examination, Treatment plan, Patient chart: medical orders
Hospital Routine Documentation Subform at the University Hospital Muenster. Original Form name: Pädiatrische Anamnese

Balance Sheet Pediatric surgery UKM - Patient admission

- 9/20/21 - 1 form, 2 itemgroups, 44 items, 2 languages
Itemgroups: Patient admission, Patient questionnaire
Balance Sheet converted to ODM format. Routine documentation of University Hospital of Münster. Publication granted by Dr. med. V. Müller

Medical history Nuclear medicine UKM - Medical history

- 9/20/21 - 1 form, 5 itemgroups, 69 items, 2 languages
Itemgroups: Patient demographics, Medical history, Eyes, Thyroid gland, Finding
Medical history form converted to ODM format. Routine documentation of University Hospital of Münster. Publication granted by Univ.-Prof. Dr. med. Michael Schäfers

Birth sheet, obstetric sheet Routine documentation in German hospitals DMI

- 9/20/21 - 1 form, 6 itemgroups, 44 items, 2 languages
Itemgroups: General information, Medical history, Medical examination, General findings, Current pregnancy, Current pregnancy complications
Routine documentation in German hospitals. Source file name: SD070109_Geburtenbogen. Examplary forms provided by DMI (http://www.dmi.de/)

Premedication Example 2 Routine documentation in German hospitals DMI

- 9/20/21 - 1 form, 20 itemgroups, 158 items, 2 languages
Itemgroups: Patient data, Physical parameters, Medical procedure, Preoperative state; risk factors, ECG, heart, lungs, circulatory system, Neurology, metabolism, Other findings, Laboratory, Blood test, Anticoagulation, assessment Preoperative, instructions preoperative, Transfusion, criteria surgery, food intake, Premedication
Routine documentation in German hospitals. Source file name: TH130110_Prämedikationsprotokoll Examplary forms provided by DMI (http://www.dmi.de/)

Premedication Example 1 Routine documentation in German hospitals DMI

- 9/20/21 - 1 form, 9 itemgroups, 74 items, 2 languages
Itemgroups: Patient data, Laboratory values, risk assessment Organ function, Preoperative assessment, Medical procedure, Checklist, Medication, Further instructions, Further information
Routine documentation in German hospitals. Source file name: TH130110_Prämedikationsprotokoll Examplary forms provided by DMI (http://www.dmi.de/)

Years 6-9 Medical & Personal History Cardiovascular Health Study (CHS)

- 9/20/21 - 1 form, 1 itemgroup, 314 items, 1 language
Itemgroup: medical history
Documentation part: Record 59 Years 6-9 Medical & Personal History The Cardiovascular Health Study (CHS) was initiated by the National Heart, Lung and Blood Institute (NHLBI) in 1987 to determine the risk factors for development and progression of cardiovascular disease (CVD) in older adults, with an emphasis on subclinical measures. The study recruited 5,888 adults aged 65 or older at entry in four U.S. communities and conducted extensive annual clinical exams between 1989-1999 along with semi-annual phone calls, events adjudication, and subsequent data analyses and publications. Additional data were collected by studies ancillary to CHS. With the exception of annual clinic visits, these activities are still ongoing. Data obtained from: https://chs-nhlbi.org/ Permission granted by: Erika Enright.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial