Informatie:
Fout:
ID
39559
Beschrijving
Observational Study on Prevalence of Host and Viral Genotypes in Chronic Hepatitis B and Hepatitis C Patients in India; ODM derived from: https://clinicaltrials.gov/show/NCT01772121
Link
https://clinicaltrials.gov/show/NCT01772121
Trefwoorden
Versies (1)
- 28-01-20 28-01-20 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
28 januari 2020
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility Hepatitis B NCT01772121
Eligibility Hepatitis B NCT01772121
- StudyEvent: Eligibility
Similar models
Eligibility Hepatitis B NCT01772121
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Informed Consent
Item
willing and able to provide written informed consent
boolean
C0021430 (UMLS CUI [1])
Age
Item
male or female, age >= 18
boolean
C0001779 (UMLS CUI [1])
Compliance behavior Trial Visits
Item
willing and able to comply with the visit procedure
boolean
C1321605 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0008952 (UMLS CUI [1,3])
C0008976 (UMLS CUI [1,2])
C0008952 (UMLS CUI [1,3])
Chronic Hepatitis C Previous | Chronic Hepatitis B Previous
Item
prior diagnosis of chronic hcv infection or chronic hbv infection
boolean
C0524910 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C0524909 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
C0205156 (UMLS CUI [1,2])
C0524909 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
Difficulty with Collection of blood specimen | Poor venous access Phlebotomy
Item
history of difficulty with blood collection and/or poor venous access for the purposes of phlebotomy
boolean
C0332218 (UMLS CUI [1,1])
C0005834 (UMLS CUI [1,2])
C0577866 (UMLS CUI [2,1])
C0190979 (UMLS CUI [2,2])
C0005834 (UMLS CUI [1,2])
C0577866 (UMLS CUI [2,1])
C0190979 (UMLS CUI [2,2])
Blood Coagulation Disorder
Item
history of bleeding disorder
boolean
C0005779 (UMLS CUI [1])
Blood Loss Requirement Transfusion | Hemoglobin decreased
Item
blood loss requiring transfusion or > 3 g/dl decrease in hemoglobin within 4 days of the visit
boolean
C3163616 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0005841 (UMLS CUI [1,3])
C0162119 (UMLS CUI [2])
C1514873 (UMLS CUI [1,2])
C0005841 (UMLS CUI [1,3])
C0162119 (UMLS CUI [2])
HCV coinfection | HBV coinfection | HIV coinfection
Item
knowingly co-infected with hcv/hbv or with hiv
boolean
C1698259 (UMLS CUI [1])
C2242656 (UMLS CUI [2])
C4062778 (UMLS CUI [3])
C2242656 (UMLS CUI [2])
C4062778 (UMLS CUI [3])
Therapy Chronic Hepatitis C | Therapy Chronic Hepatitis B
Item
currently undergoing therapy for chronic hepatitis c or chronic hepatitis b
boolean
C0087111 (UMLS CUI [1,1])
C0524910 (UMLS CUI [1,2])
C0087111 (UMLS CUI [2,1])
C0524909 (UMLS CUI [2,2])
C0524910 (UMLS CUI [1,2])
C0087111 (UMLS CUI [2,1])
C0524909 (UMLS CUI [2,2])
Investigational New Drugs | Investigational Medical Device
Item
currently receiving treatment with any other investigational agent or device --
boolean
C0013230 (UMLS CUI [1])
C2346570 (UMLS CUI [2])
C2346570 (UMLS CUI [2])
Study Subject Participation Status | Clinical Trial Evaluation Therapy | Clinical Trial Evaluation Procedure
Item
enrolled in another clinical study evaluating a treatment or procedure
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C1261322 (UMLS CUI [2,2])
C0087111 (UMLS CUI [2,3])
C0008976 (UMLS CUI [3,1])
C1261322 (UMLS CUI [3,2])
C0184661 (UMLS CUI [3,3])
C0008976 (UMLS CUI [2,1])
C1261322 (UMLS CUI [2,2])
C0087111 (UMLS CUI [2,3])
C0008976 (UMLS CUI [3,1])
C1261322 (UMLS CUI [3,2])
C0184661 (UMLS CUI [3,3])