ID

24586

Description

Study part: Concomitant Medications (CONMEDS). A 52-Week, Open-Label Study to Assess the Long-Term Safety of Ropinirole Extended Release (XR) in Patients with Restless Legs Syndrome (RLS). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Clinicaltrials.gov Identifier: NCT00355641. 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. Study ID: 101468/206. Clinical Study ID: 101468/206.

Mots-clés

Versions (1)
  1. 07/08/2017 07/08/2017 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

7 août 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
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Concomitant Medications (CONMEDS) Ropinirole Restless Legs Syndrom NCT00355641

Anglais

Concomitant Medications (CONMEDS)

1 Formulaires  
CONCOMITANT MEDICATIONS
Description

CONCOMITANT MEDICATIONS

Alias
UMLS CUI-1
C2347852
Sequence Number
Description

Sequence Number

Type de données

text

Alias
UMLS CUI [1]
C2348184
1. Drug Name
Description

(Trade Name preferred)

Type de données

text

Alias
UMLS CUI [1]
C0013227
2. Modified reported term
Description

Modified reported term

Type de données

text

Alias
UMLS CUI [1]
C2826819
GSK Drug synonym
Description

Drug synonym

Type de données

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0871468
GSK Drug Collection code
Description

Drug Collection code

Type de données

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C1516698
UMLS CUI [1,3]
C0805701
Failed coding
Description

Failed coding Concomitant Agent

Type de données

text

Alias
UMLS CUI [1,1]
C0805701
UMLS CUI [1,2]
C0231175
UMLS CUI [1,3]
C2347852
3. Reason for Medication
Description

Reason for Medication

Type de données

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0013227
4. Start Date
Description

Start Date

Type de données

date

Alias
UMLS CUI [1]
C0808070
5. Taken Prior to Study?
Description

Taken Prior to Study?

Type de données

boolean

Alias
UMLS CUI [1]
C2826667
6. Ongoing?
Description

Ongoing?

Type de données

text

Alias
UMLS CUI [1,1]
C0549178
UMLS CUI [1,2]
C2347852
Medication Type
Description

Medication Type

Type de données

text

Alias
UMLS CUI [1,1]
C0332307
UMLS CUI [1,2]
C0013227
Retour au début de la page

Similar models

Concomitant Medications (CONMEDS)

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
CONCOMITANT MEDICATIONS
C2347852 (UMLS CUI-1)
Sequence Number
Item
Sequence Number
text
C2348184 (UMLS CUI [1])
Drug Name
Item
1. Drug Name
text
C0013227 (UMLS CUI [1])
Modified reported term
Item
2. Modified reported term
text
C2826819 (UMLS CUI [1])
Drug synonym
Item
GSK Drug synonym
text
C0013227 (UMLS CUI [1,1])
C0871468 (UMLS CUI [1,2])
Drug Collection code
Item
GSK Drug Collection code
text
C0013227 (UMLS CUI [1,1])
C1516698 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
Failed coding Concomitant Agent
Item
Failed coding
text
C0805701 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,3])
Reason for Medication
Item
3. Reason for Medication
text
C0392360 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Start Date
Item
4. Start Date
date
C0808070 (UMLS CUI [1])
Taken Prior to Study?
Item
5. Taken Prior to Study?
boolean
C2826667 (UMLS CUI [1])
Ongoing?
Item
6. Ongoing?
text
C0549178 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Medication Type
Item
Medication Type
text
C0332307 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Retour au début de la page 

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