Informatie:
Fout:
ID
12931
Beschrijving
Long-Term Therapy With Ribavirin for Chronic Hepatitis C; ODM derived from: https://clinicaltrials.gov/show/NCT00001854
Link
https://clinicaltrials.gov/show/NCT00001854
Trefwoorden
Versies (1)
- 06-01-16 06-01-16 -
Houder van rechten
CC BY-NC 3.0
Geüploaded op
6 januari 2016
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY-NC 3.0
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 Chronic Hepatitis C NCT00001854
Eligibility Chronic Hepatitis C NCT00001854
- StudyEvent: Eligibility
Similar models
Eligibility Chronic Hepatitis C NCT00001854
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
age above 18 years, male or female.
Item
age above 18 years, male or female.
boolean
C0001779 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
C0079399 (UMLS CUI [2])
elevated alanine (alt) or asparate (ast) aminotransferase activities
Item
elevated alanine (alt) or asparate (ast) aminotransferase activities averaging at least twice the upper limit of normal on three determinations taken at least one month apart during the previous 6 months. the mean of these three determinations will be defined as "baseline" alt and ast levels.
boolean
C0201836 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
C0201899 (UMLS CUI [2])
anti-hcv and hcv rna
Item
presence of anti-hcv and hcv rna in serum tested at least once during the previous six months.
boolean
C0019196 (UMLS CUI [1])
evidence of chronic hepatitis on liver biopsy done within the previous 12 months with a histology activity index of at least 6 (out of a maximum of 22).
Item
evidence of chronic hepatitis on liver biopsy done within the previous 12 months with a histology activity index of at least 6 (out of a maximum of 22).
boolean
C0019196 (UMLS CUI [1])
Interferon
Item
contraindications to the use of alpha interferon, either in the form of specific contraindications to its use (depression, psychiatric illness, neurological impairment, severe thrombocytopenia, autoimmune disease), or the history of severe side effects or intolerance during a previous course of alpha interferon, or lack of a sustained virological (sustained lost of hcv rna from serum for more than six months after stopping treatment) response to an adequate course (6 months) of the combination of alpha interferon and ribavirin or (after september 1, 2003) the combination of peginterferon and ribavirin.
boolean
C1610033 (UMLS CUI [1])
C0035525 (UMLS CUI [2])
C0982327 (UMLS CUI [3])
C0035525 (UMLS CUI [2])
C0982327 (UMLS CUI [3])
written informed consent.
Item
written informed consent.
boolean
C0021430 (UMLS CUI [1])
inclusion criteria for patients in 98-dk-0003:
Item
inclusion criteria for patients in 98-dk-0003:
boolean
C1512693 (UMLS CUI [1])
clinical research protocol 98-dk-0003
Item
an important group of patients who were enrolled in the current study, were patients who participated in the clinical research protocol 98-dk-0003 (combination of alpha interferon with long-term ribavirin for patients with chronic hepatitis c) and who did not have a sustained virological response to this treatment. these patients were eligible to enroll into the current study once they had finished the therapy and follow up period in that trial. these patients fit the inclusion criteria listed above with one exception: some patients were receiving ribavirin monotherapy as a part of their participation in 98-dk-0003. these patients were eligible to be immediately enrolled into this study without a medication-free period in between.
boolean
pregancy and contraception
Item
pregancy or, in women of childbearing potential, inability to practice adequate contraception. men with spouses or sexual partners of childbearing potential also be excluded if they are unable to practice adequate contraception.
boolean
C0032961 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
C0700589 (UMLS CUI [2])
significant systemic illnesses
Item
significant systemic illnesses other than liver disease, including a history of congestive heart failure, cerebral vascular disease, renal failure (creatinine clearance less than 50 ml/min), and angina pectoris.
boolean
C0009488 (UMLS CUI [1])
abnormal stress test or carotid untrasound
Item
patients with an abnormal stress test or carotid untrasound will not be enrolled into this study.
boolean
C1384495 (UMLS CUI [1])
C0948945 (UMLS CUI [2])
C0948945 (UMLS CUI [2])
anemia
Item
pre-existing anemia (hematocrit less than 32%) or known history of hemolytic anemia.
boolean
C0002871 (UMLS CUI [1])
interferon or immunosuppressive therapy
Item
interferon or immunosuppressive therapy within the last 6 months.
boolean
C3652465 (UMLS CUI [1])
C0021081 (UMLS CUI [2])
C0021081 (UMLS CUI [2])
liver disease
Item
evidence of another form of liver disease in addition to viral hepatitis, such as autoimmune or alcoholic liver disease.
boolean
C0023895 (UMLS CUI [1])
active or recent (within one year) alcohol or drug abuse or psychiatric illness that is likely to interfere with compliance and requirements for safety monitoring during this study.
Item
active or recent (within one year) alcohol or drug abuse or psychiatric illness that is likely to interfere with compliance and requirements for safety monitoring during this study.
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])