ID
35462
Descripción
Study ID: 101468/194 Clinical Study ID: 101468/194 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: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: requip Study Indication: Restless Legs Syndrome
Palabras clave
Versiones (1)
- 5/3/19 5/3/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
5 de marzo de 2019
DOI
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Licencia
Creative Commons BY-NC 3.0
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Ropinirole in Patients with Restless Legs Syndrome (Study ID: 101468/194)
Screening Repeat Tests
- StudyEvent: ODM
Descripción
Electrocardiogram (12 Lead)
Alias
- UMLS CUI-1
- C0430456
Descripción
12 lead ECG, Date in time
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0430456
- UMLS CUI [1,2]
- C0011008
Descripción
If ’Yes’, please record details in the Baseline Signs and Symptoms and/or SAE section at the back of this book and exclude the patient from the study.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0430456
- UMLS CUI [1,2]
- C1704258
Descripción
Physical Examination
Alias
- UMLS CUI-1
- C0031809
Descripción
Laboratory Evaluation
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0220825
Descripción
Collection of blood specimen for laboratory procedure, Date in time
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0011008
Descripción
Laboratory Procedures, Laboratory specimen identification label
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0022885
- UMLS CUI [1,2]
- C4273937
Descripción
If ‘Yes’, please record the findings and/or diagnosis in the Baseline Signs and Symptoms and/or SAE section at the back of this book and exclude the patient from the study.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0022885
- UMLS CUI [1,2]
- C1704258
Descripción
Urine Dipstick
Alias
- UMLS CUI-1
- C0430370
Descripción
If ’Positive’, please record details on the Significant Medical/Surgical History and Physical Examination or Baseline Signs and Symptoms/SAE pages and send a sample to Quest Diagnostics for further evaluation.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0430370
- UMLS CUI [1,2]
- C0456984
Similar models
Screening Repeat Tests
- StudyEvent: ODM
C1300638 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1704258 (UMLS CUI [1,2])
C0220825 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C4273937 (UMLS CUI [1,2])
C1704258 (UMLS CUI [1,2])
C0456984 (UMLS CUI [1,2])