ID
35142
Beschrijving
Study ID: 101468/205 Clinical Study ID: 101468/205 Study Title:A 12-Week, Double-Blind, Placebo Controlled, Parallel Group Study to Assess the Efficacy and Safety of Ropinirole XR (Extended Release) in Patients with Restless Legs Syndrome Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00197080 Sponsor: GlaxoSmithKline Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara; Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication: Restless Legs Syndrome
Trefwoorden
Versies (1)
- 19-02-19 19-02-19 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
19 februari 2019
DOI
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Licentie
Creative Commons BY-NC 3.0
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Efficacy and Safety of Ropinirole XR (Extended Release) in Patients with Restless Legs Syndrome NCT00197080
Pregnancy Information; Study Conclusion; Investigator Comment Log; Investigator's Signature
Beschrijving
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Beschrijving
Date of subject completion or withdrawal
Datatype
date
Alias
- UMLS CUI [1]
- C2983670
Beschrijving
If Yes, check the primary reason for withdrawal
Datatype
boolean
Alias
- UMLS CUI [1]
- C0422727
Beschrijving
If Adverse Event, r ecord details on the Non-Serious Adverse Events or Serious Adverse Event pages as appropriate.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0392360
Beschrijving
If other reason for withdrawal, specify.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Beschrijving
Administrative
Alias
- UMLS CUI-1
- C1320722
Beschrijving
Investigator Comment Log
Alias
- UMLS CUI-1
- C0008961
- UMLS CUI-2
- C0947611
Beschrijving
Investigator's Signature
Alias
- UMLS CUI-1
- C2346576
Beschrijving
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.
Datatype
text
Alias
- UMLS CUI [1]
- C2346576
Beschrijving
Investigator’s name (print)
Datatype
text
Alias
- UMLS CUI [1]
- C2826892
Beschrijving
Date
Datatype
date
Alias
- UMLS CUI [1]
- C0011008
Similar models
Pregnancy Information; Study Conclusion; Investigator Comment Log; Investigator's Signature
C0392360 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
C0947611 (UMLS CUI-2)
C1516308 (UMLS CUI [1,2])