ID

27273

Beskrivning

Study ID: 101468/188 Clinical Study ID: SKF-101468/188 Study Title:A Study of the Maintained Efficacy and Safety of Ropinirole Versus Placebo in the Long Term Treatment of Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication: Parkinson Disease Module: Study Conclusion

Nyckelord

Versioner (1)
  1. 2017-11-06 2017-11-06 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

6 november 2017

DOI

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Licens

Creative Commons BY-NC 3.0
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GSK Ropinirole in Patients Suffering from Restless Legs Syndrome 101468/188

Engelsk

Study Conclusion

1 Formulär  
  1. StudyEvent: ODM
    1. Study Conclusion
Study Conclusion
Beskrivning

Study Conclusion

Alias
UMLS CUI-1
C2348568
UMLS CUI-2
C1707478
UMLS CUI-3
C0008976
UMLS CUI-4
C0035258
Did the patient complete the study according to the protocol?
Beskrivning

End of Study

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0444496
If ’No’, please mark the primary cause of withdrawal. (Mark one box only)
Beskrivning

primary cause of withdrawal

Datatyp

integer

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C0392360
Primary cause of withdrawal: If 'Other', please specify
Beskrivning

primary cause of withdrawal

Datatyp

text

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C0392360
Investigator’s Signature
Beskrivning

Investigator’s Signature

Datatyp

text

Alias
UMLS CUI [1]
C2346576
Investigator’s Signature Date
Beskrivning

Investigator’s Signature Date

Datatyp

date

Alias
UMLS CUI [1,1]
C2346576
UMLS CUI [1,2]
C0011008
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Similar models

Study Conclusion

1 Formulär
  1. StudyEvent: ODM
    1. Study Conclusion
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Study Conclusion
C2348568 (UMLS CUI-1)
C1707478 (UMLS CUI-2)
C0008976 (UMLS CUI-3)
C0035258 (UMLS CUI-4)
End of Study
Item
Did the patient complete the study according to the protocol?
boolean
C2348568 (UMLS CUI [1,1])
C0444496 (UMLS CUI [1,2])
Item
If ’No’, please mark the primary cause of withdrawal. (Mark one box only)
integer
C0422727 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
primary cause of withdrawal
Code List
If ’No’, please mark the primary cause of withdrawal. (Mark one box only)
CL Item
Adverse experience (please complete AE page)  (1)
CL Item
Insufficient therapeutic effect (2)
CL Item
Protocol deviation (including non-compliance) (3)
CL Item
Lost to follow-up (4)
CL Item
Other (5)
primary cause of withdrawal
Item
Primary cause of withdrawal: If 'Other', please specify
text
C0422727 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Investigator’s Signature
Item
Investigator’s Signature
text
C2346576 (UMLS CUI [1])
Investigator’s Signature Date
Item
Investigator’s Signature Date
date
C2346576 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Tillbaka till toppen 

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