1. StudyEvent: combicare trial
    1. Screening
    2. Intervention
    3. POD 3
    4. POD 7
    5. POD 14 / Discharge
    6. POD 30
    7. POD 60/Discontinuation
    8. Signature
  2. StudyEvent: Readmission To Hospital
    1. Readmission To Hospital
  3. StudyEvent: Adverse Events
    1. Adverse Events
  4. StudyEvent: Concomitant Medication
    1. Concomitant Medication
  5. StudyEvent: Protocol Violation
    1. Protocol violation
Investigator's statement
Descripción

Investigator's statement

Alias
UMLS CUI [1,1]
C2346576
I confirm that all data entered in the eCRF are complete and accurate at the best of my knowledge
Descripción

confirmation

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0750484
Investigator's signature
Descripción

Investigator's signature

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2346576

Similar models

  1. StudyEvent: combicare trial
    1. Screening
    2. Intervention
    3. POD 3
    4. POD 7
    5. POD 14 / Discharge
    6. POD 30
    7. POD 60/Discontinuation
    8. Signature
  2. StudyEvent: Readmission To Hospital
    1. Readmission To Hospital
  3. StudyEvent: Adverse Events
    1. Adverse Events
  4. StudyEvent: Concomitant Medication
    1. Concomitant Medication
  5. StudyEvent: Protocol Violation
    1. Protocol violation
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Investigator's statement
C2346576 (UMLS CUI [1,1])
confirmation
Item
I confirm that all data entered in the eCRF are complete and accurate at the best of my knowledge
boolean
C0750484 (UMLS CUI [1,1])
Investigator's signature
Item
Investigator's signature
text
C2346576 (UMLS CUI [1,1])