ID
35462
Description
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
Mots-clés
Versions (1)
- 05/03/2019 05/03/2019 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
5 mars 2019
DOI
Pour une demande vous connecter.
Licence
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
Description
Electrocardiogram (12 Lead)
Alias
- UMLS CUI-1
- C0430456
Description
12 lead ECG, Date in time
Type de données
date
Alias
- UMLS CUI [1,1]
- C0430456
- UMLS CUI [1,2]
- C0011008
Description
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.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0430456
- UMLS CUI [1,2]
- C1704258
Description
Physical Examination
Alias
- UMLS CUI-1
- C0031809
Description
Laboratory Evaluation
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0220825
Description
Collection of blood specimen for laboratory procedure, Date in time
Type de données
date
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0011008
Description
Laboratory Procedures, Laboratory specimen identification label
Type de données
text
Alias
- UMLS CUI [1,1]
- C0022885
- UMLS CUI [1,2]
- C4273937
Description
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.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0022885
- UMLS CUI [1,2]
- C1704258
Description
Urine Dipstick
Alias
- UMLS CUI-1
- C0430370
Description
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.
Type de données
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])