ID
40761
Descripción
Study ID: 101468/218 Clinical Study ID: SKF-101468/218 Study Title:A Single-Blind, Randomised, Placebo-Controlled, Parallel-Group, Multicentre, Phase IIa Study to Determine the Pharmacokinetics and Tolerability of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: requip Study Indication: Restless Legs Syndrome
Palabras clave
Versiones (1)
- 8/5/20 8/5/20 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
8 de mayo de 2020
DOI
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Licencia
Creative Commons BY-NC 4.0
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Pharmacokinetics and Tolerability of Ropinirole in Patients Suffering from Restless Legs Syndrome 101468/218
Pregnancy Information; Study Conclusion, Investigator's Statement (Follow-Up)
Descripción
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Descripción
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Descripción
Did the subject complete the study as planned?
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C2348577
Descripción
If the subject did not complete the study as planned, mark the most appropriate category
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C2348577
- UMLS CUI [1,2]
- C2826287
Descripción
Other reason for not completing the study as planned
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2348577
- UMLS CUI [1,2]
- C2826287
- UMLS CUI [1,3]
- C0205394
Descripción
Comments on reason for withdrawal:
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0947611
- UMLS CUI [1,2]
- C2349954
- UMLS CUI [1,3]
- C0566251
Descripción
Date of Withdrawal:
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C0011008
Descripción
Time of Withdrawal:
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C0040223
Descripción
Date of Final Dose:
Tipo de datos
date
Alias
- UMLS CUI [1]
- C1762893
Descripción
Time of Final Dose:
Tipo de datos
time
Alias
- UMLS CUI [1]
- C0946444
Descripción
Investigator's Statement
Alias
- UMLS CUI-1
- C0008961
- UMLS CUI-2
- C1710187
Descripción
Check all Adverse Event forms are up to date and complete
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0920316
- UMLS CUI [1,3]
- C0205197
Descripción
Check that the Concomitant Medication form is up to date
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0920316
- UMLS CUI [1,3]
- C0237400
Descripción
Check that all appropriate pages are signed (thus indicating completion) and dated
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0805732
- UMLS CUI [1,2]
- C1283174
Descripción
Check that laboratory results are included
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1254595
- UMLS CUI [1,2]
- C0920316
Descripción
I certify that the observations and findings are recorded correctly and completely in this CRF.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2346576
Descripción
Investigator's Signature Date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Similar models
Pregnancy Information; Study Conclusion, Investigator's Statement (Follow-Up)
C0019994 (UMLS CUI [1,2])
C2826287 (UMLS CUI [1,2])
C2826287 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2349954 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C1710187 (UMLS CUI-2)
C0920316 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
C0920316 (UMLS CUI [1,2])
C0237400 (UMLS CUI [1,3])
C1283174 (UMLS CUI [1,2])
C0920316 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])