Informationen: Dieses ist nicht die aktuellste Version des Datenmodells. Eine Versionsübersicht finden Sie links unter Versionen. Die aktuellste Version finden Sie hier.
Informationen:
Fehler:
ID
21989
Beschreibung
A Study of the Pharmacokinetics and Immunologic Effects of Lipoic Acid in Multiple Sclerosis; ODM derived from: https://clinicaltrials.gov/show/NCT00676156
Link
https://clinicaltrials.gov/show/NCT00676156
Stichworte
Versionen (2)
- 13.05.17 13.05.17 -
- 13.05.17 13.05.17 -
Hochgeladen am
13. Mai 2017
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY-NC 3.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Eligibility Multiple Sclerosis NCT00676156
Eligibility Multiple Sclerosis NCT00676156
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Multiple Sclerosis NCT00676156
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Multiple Sclerosis
Item
definite ms by mcdonald's or poser's criteria
boolean
C0026769 (UMLS CUI [1])
Kurtzke multiple sclerosis rating scale
Item
edss ≤ 7.5
boolean
C0451246 (UMLS CUI [1])
Age
Item
age 18 to 80
boolean
C0001779 (UMLS CUI [1])
Exacerbation of multiple sclerosis
Item
no clinically significant ms exacerbation within 30 days of the screening
boolean
C0581392 (UMLS CUI [1])
CORTICOSTEROIDS FOR SYSTEMIC USE
Item
no systemically administered corticosteroids within 30 days of study entry
boolean
C3653708 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
patient not pregnant or breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
ID.7
Item
no la in previous 2 weeks
boolean
Anticoagulants | Heparin | Coumadin | Aspirin
Item
not on anti-coagulants such as heparin, coumadin, or aspirin during study
boolean
C0003280 (UMLS CUI [1])
C0019134 (UMLS CUI [2])
C0699129 (UMLS CUI [3])
C0004057 (UMLS CUI [4])
C0019134 (UMLS CUI [2])
C0699129 (UMLS CUI [3])
C0004057 (UMLS CUI [4])
Disease At risk Adverse event | Coronary heart disease | Liver diseases | Lung diseases | Diabetes Mellitus
Item
no other significant health problem (e.g. active coronary heart disease, liver disease, pulmonary disease, diabetes mellitus) that might increase risk of patient experiencing adverse events
boolean
C0012634 (UMLS CUI [1,1])
C1444641 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,3])
C0010068 (UMLS CUI [2])
C0023895 (UMLS CUI [3])
C0024115 (UMLS CUI [4])
C0011849 (UMLS CUI [5])
C1444641 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,3])
C0010068 (UMLS CUI [2])
C0023895 (UMLS CUI [3])
C0024115 (UMLS CUI [4])
C0011849 (UMLS CUI [5])
Informed Consent Unable
Item
inability to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,2])
Condition Study Subject Participation Status Inappropriate
Item
any condition which would make the patient, in the opinion of the investigator, unsuitable for the study
boolean
C0348080 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])
C2348568 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])