ID
35688
Description
Study ID: 101468/192 Clinical Study ID: 101468/192 Study Title:A 52 Week Open-Label Extension Study of the Long-Term Safety of Ropinirole in Subjects Suffering from 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: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara; Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication : Restless Legs Syndrome The study consists of 16 visits which are devided in 3 study books: Book 1: Screening (+Baseline), Day 2, Week 1, Week 2 , Week 3 , Week 4, Week 5, Week 6, Week 7, Week 8 Book 2: Week 12, Week 24, Week 36, Week 48, Week 52, Follow-up Book 3: Early withdrawal and Follow-up Each follow-up Visit takes place 7 +/- 3 days after last dose This document contains the study conclusion form. It has to be filled in for the end of study or for early withdrawal.
Mots-clés
Versions (1)
- 15/03/2019 15/03/2019 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
15 mars 2019
DOI
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Licence
Creative Commons BY-NC 3.0
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Long-Term Safety of Ropinirole in Subjects Suffering from Restless Legs Syndrome (RLS), 101468/192
Study Conclusion
- StudyEvent: ODM
Description
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Description
Study Conclusion
Type de données
text
Alias
- UMLS CUI [1,1]
- C1707478
- UMLS CUI [1,2]
- C0008972
Description
Reason of withdrawal
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0085978
Description
Other reason
Type de données
text
Alias
- UMLS CUI [1]
- C3840932
Description
Serious Adverse Experiences
Alias
- UMLS CUI-1
- C1519255
Description
Person Reporting SAE
Type de données
text
Alias
- UMLS CUI [1]
- C0008961
Description
AEGIS Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0237753
- UMLS CUI [1,2]
- C0600091
Description
Serious Adverse Experience
Type de données
text
Alias
- UMLS CUI [1]
- C1519255
Description
Specify reason(s) for considering this a serious AE
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0011065
Description
Specify reason(s) for considering this a serious AE
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C2826244
Description
Specify reason(s) for considering this a serious AE
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0019993
Description
Specify reason(s) for considering this a serious AE
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0231170
Description
Specify reason(s) for considering this a serious AE
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0000768
Description
Specify reason(s) for considering this a serious AE
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0205394
Description
Other reason, specification
Type de données
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C3840932
- UMLS CUI [1,3]
- C1521902
Description
day month year 00:00-23:59
Type de données
datetime
Alias
- UMLS CUI [1]
- C2826806
Description
day month year 00:00-23:59
Type de données
datetime
Alias
- UMLS CUI [1]
- C2826793
Description
If patient died, STOP: go to SAE section and follow instructions given there
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1705586
- UMLS CUI [1,2]
- C1519255
Description
Experience Course
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0750729
Description
Number of episodes
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C4086638
Description
Action Taken with Respect to Investigational Drug
Type de données
integer
Alias
- UMLS CUI [1]
- C2826626
Description
SAE abate
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C3853704
Description
dosage change
Type de données
text
Alias
- UMLS CUI [1]
- C0420247
Description
Serious Adverse Experiences recurrence
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0034897
Description
Relationship to Investigational Drug
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0013230
- UMLS CUI [1,3]
- C0439849
Description
Relationship to Investigational Drug
Type de données
integer
Description
Another drug
Type de données
text
Alias
- UMLS CUI [1]
- C1115771
Description
If ‘Yes’, record details in the Concomitant Medication section and/or Healthcare Resource Utilisation form if appropriate
Type de données
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0087111
Description
patient withdrawn due to this specific AE
Type de données
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C1518404
Description
Relevant Laboratory Data
Alias
- UMLS CUI-1
- C0022877
Description
Test
Type de données
text
Alias
- UMLS CUI [1,1]
- C0022885
- UMLS CUI [1,2]
- C0332307
Description
day month year
Type de données
date
Alias
- UMLS CUI [1]
- C0011008
Description
Value
Type de données
text
Alias
- UMLS CUI [1]
- C1522609
Description
Units
Type de données
text
Alias
- UMLS CUI [1]
- C1519795
Description
Normal Range
Type de données
text
Alias
- UMLS CUI [1]
- C0086715
Description
Remarks
Type de données
text
Alias
- UMLS CUI [1]
- C0947611
Description
randomisation code broken
Type de données
text
Alias
- UMLS CUI [1,1]
- C3897778
- UMLS CUI [1,2]
- C1272691
Description
Randomisation Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0034656
- UMLS CUI [1,2]
- C0237753
Description
Investigators Signature
Type de données
text
Alias
- UMLS CUI [1]
- C2346576
Description
day month year
Type de données
date
Alias
- UMLS CUI [1]
- C0011008
Description
Investigator's Name
Type de données
text
Alias
- UMLS CUI [1]
- C2826892
Description
Medical Monitor’s Signature
Type de données
text
Alias
- UMLS CUI [1]
- C2346576
Description
Medical Monitor's Name
Type de données
text
Alias
- UMLS CUI [1,1]
- C0027365
- UMLS CUI [1,2]
- C1708968
Description
day month year
Type de données
date
Alias
- UMLS CUI [1,1]
- C0807937
- UMLS CUI [1,2]
- C1708968
Similar models
Study Conclusion
- StudyEvent: ODM
C0019994 (UMLS CUI [1,2])
C0008972 (UMLS CUI [1,2])
C0085978 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,2])
C0011065 (UMLS CUI [1,2])
C2826244 (UMLS CUI [1,2])
C0019993 (UMLS CUI [1,2])
C0231170 (UMLS CUI [1,2])
C0000768 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C3840932 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
C0750729 (UMLS CUI [1,2])
C4086638 (UMLS CUI [1,2])
C0034897 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C1518404 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,2])
C1272691 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,2])
C1708968 (UMLS CUI [1,2])
C1708968 (UMLS CUI [1,2])