Englisch

Study conclusion

1 Formulare  
  1. StudyEvent: ODM
    1. Study conclusion
Study conclusion
Beschreibung

Study conclusion

Date of last contact
Beschreibung

Date of last contact

Datentyp

date

Was the subject withdrawn from the study?
Beschreibung

Was the subject withdrawn from the study?

Datentyp

text

if "Yes" choose one primary reason for withdrawal:
Beschreibung

if "Yes" choose one primary reason for withdrawal:

Datentyp

text

Date of decision to withdraw
Beschreibung

Date of decision to withdraw

Datentyp

date

Investigator comment log
Beschreibung

Investigator comment log

Only use this form to record explanatory information on anomalies such as missing data, departures from planned investigational product administration or missed visits.
Beschreibung

Only use this form to record explanatory information on anomalies such as missing data, departures from planned investigational product administration or missed visits.

Datentyp

text

CRF page number
Beschreibung

if applicable

Datentyp

integer

Comment
Beschreibung

Comment

Datentyp

text

Investigator's signature
Beschreibung

Investigator's signature

Investigator's signature
Beschreibung

I confirm that I have reviewed the data in this Case Report Form for this subject. All information entered by myself or my colleagues is, to the best of my knowledge, complete and accurate, as of the date below

Datentyp

text

Investigator's name
Beschreibung

Print

Datentyp

text

Date
Beschreibung

Date

Datentyp

date

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Ähnliche Modelle

Study conclusion

1 Formulare
  1. StudyEvent: ODM
    1. Study conclusion
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Study conclusion
Date of last contact
Item
Date of last contact
date
Item
Was the subject withdrawn from the study?
text
Was the subject withdrawn from the study?
Code List
Was the subject withdrawn from the study?
CL Item
Yes (1)
CL Item
No (2)
Item
if "Yes" choose one primary reason for withdrawal:
text
if "Yes" choose one primary reason for withdrawal:
Code List
if "Yes" choose one primary reason for withdrawal:
CL Item
[1] Adverse event -> Record retails on the Non-Serious Adverse Events or Serious Adverse Events pages as appropriate (1)
CL Item
[3] Protocol deviation (2)
CL Item
[5] Study closed/terminated (3)
CL Item
[6] Lost to follow-up (4)
CL Item
[8] Withdrew consent (Only choose when none of the primary reasons are appropriate) (5)
Date of decision to withdraw
Item
Date of decision to withdraw
date
Item Group
Investigator comment log
Only use this form to record explanatory information on anomalies such as missing data, departures from planned investigational product administration or missed visits.
Item
Only use this form to record explanatory information on anomalies such as missing data, departures from planned investigational product administration or missed visits.
text
CRF page number
Item
CRF page number
integer
Comment
Item
Comment
text
Item Group
Investigator's signature
Investigator's signature
Item
Investigator's signature
text
Investigator's name
Item
Investigator's name
text
Date
Item
Date
date
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