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  1. 1. Klinische studie
  2. 2. Routinedocumentatie
  3. 3. Register-/kohortstudies
  4. 4. Kwaliteitswaarborging
  5. 5. Datastandaard
  6. 6. Patiëntenvragenlijst
  7. 7. Medisch vakgebied
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- 25-07-17 - 1 Formulier, 26 Itemgroepen, 74 Data-elementen, 1 Taal
Itemgroepen: Study entry, Vital signs, Medical Procedures, Concomitant Medication, Adverse reaction, Exclusion Criterion, Healthcare resource utilisation - visits/contacts with physician, Healthcare resource utilisation - visits/contacts with physician, Healthcare resource utilisation - Visits/Contacts with other Paramedical Practitioners, Healthcare resource utilisation - Visits/Contacts with other Paramedical Practitioners, Healthcare resource utilisation - Hospitalisation, Healthcare resource utilisation - hospitalisation, Healthcare resource utilisation - accident & emergency / emergency room visits, Healthcare resource utilisation - accident & emergency / emergency room visits, Clinical Global impression, RLS Rating scale, Patient rated scale, Pregnancy information, Study Subject Participation Status, Investigator signature, Orthostatic vital signs, Pre-Dose Reading 1, Pre-Dose Reading 2, Pre-Dose Reading 3, Time of dose, 2 hours Post-Dose Reading 1

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