ID
35142
Descripción
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
Palabras clave
Versiones (1)
- 19/2/19 19/2/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
19 de febrero de 2019
DOI
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Licencia
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
Descripción
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Descripción
Date of subject completion or withdrawal
Tipo de datos
date
Alias
- UMLS CUI [1]
- C2983670
Descripción
If Yes, check the primary reason for withdrawal
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0422727
Descripción
If Adverse Event, r ecord details on the Non-Serious Adverse Events or Serious Adverse Event pages as appropriate.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0392360
Descripción
If other reason for withdrawal, specify.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Descripción
Administrative
Alias
- UMLS CUI-1
- C1320722
Descripción
Investigator Comment Log
Alias
- UMLS CUI-1
- C0008961
- UMLS CUI-2
- C0947611
Descripción
Investigator's Signature
Alias
- UMLS CUI-1
- C2346576
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2346576
Descripción
Investigator’s name (print)
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2826892
Descripción
Date
Tipo de datos
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])