ID
29078
Description
Study ID: 101468/249 Clinical Study ID: 101468/249 Study Title: A 12-Week, Double-Blind, Placebo Controlled, Parallel Group Study to Assess the Efficacy and Safety of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00363857 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: N/A 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; Restless Legs Syndrome (RLS)
Mots-clés
Versions (1)
- 23/02/2018 23/02/2018 -
Détendeur de droits
GlaxoSmithKline (GSK)
Téléchargé le
23 février 2018
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
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Clinical Study, Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS), Study ID: 101468/249, NCT00363857
Assessment Week2
- StudyEvent: ODM
Description
IRLS Rating Scale
Alias
- UMLS CUI-1
- C0681889
- UMLS CUI-2
- C0035258
Description
Orthostatic vital signs
Alias
- UMLS CUI-1
- C0518766
Description
Orthostatic vital signs
Type de données
integer
Alias
- UMLS CUI [1]
- C0518766
Description
Time Vitals Taken
Type de données
time
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0040223
Description
Blood pressure
Type de données
integer
Unités de mesure
- mmHg
Alias
- UMLS CUI [1]
- C0005823
Description
Pulse
Type de données
integer
Unités de mesure
- beats/min
Alias
- UMLS CUI [1]
- C0232117
Description
Please record any medical procedures performed since the last visit in the Medical Procedures section at the back of this book.
Alias
- UMLS CUI-1
- C0199171
Description
Please record any changes in concomitant medication since the last visit in the Concomitant Medication section at the back of this book.
Alias
- UMLS CUI-1
- C2347852
Description
Please record any adverse experiences observed or elicited by the following direct question to the patient: "Have you felt different in any way since the last visit?" in the Adverse Experience and/or SAE section at the back of this book.
Alias
- UMLS CUI-1
- C0877248
Description
Clinical Global Impressions
Alias
- UMLS CUI-1
- C3639708
Description
If the patient requires a dose reduction between this and the next visit please complete the Study Medication Record and Dose Reductions Due To Adverse Experiences pages at the back of this book.
Alias
- UMLS CUI-1
- C0178602
- UMLS CUI-2
- C0547047
Description
Ramos Dispensing
Alias
- UMLS CUI-1
- C0034656
- UMLS CUI-2
- C0947323
Similar models
Assessment Week2
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])
C0035258 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C0547047 (UMLS CUI-2)
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