ID

29720

Beschreibung

Directly Observed Hepatitis C Treatment in Methadone Clinics; ODM derived from: https://clinicaltrials.gov/show/NCT01442311

Link

https://clinicaltrials.gov/show/NCT01442311

Stichworte

  1. 16.04.18 16.04.18 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

16. April 2018

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Hepatitis C NCT01442311

Eligibility Hepatitis C NCT01442311

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
hcv-infected
Beschreibung

Hepatitis C

Datentyp

boolean

Alias
UMLS CUI [1]
C0019196
receive hcv medical care at the methadone clinic
Beschreibung

Medical care Hepatitis C Methadone Clinic

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0496675
UMLS CUI [1,2]
C0019196
UMLS CUI [1,3]
C1552533
plan to initiate hcv treatment on-site within the next 3 months
Beschreibung

Therapeutic procedure Hepatitis C Study Site Planned

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0019196
UMLS CUI [1,3]
C2825164
UMLS CUI [1,4]
C1301732
psychiatrically stable as determined by hcv treatment provider and/or on-site psychiatrist
Beschreibung

Stable status Psychiatric

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0205360
UMLS CUI [1,2]
C0205487
attend the methadone clinic between three and six days per week to receive methadone
Beschreibung

Methadone Receive days per week

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0025605
UMLS CUI [1,2]
C1514756
UMLS CUI [1,3]
C0677547
stable dose fo methadone for two weeks prior to the baseline visit
Beschreibung

Methadone Dose Stable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0025605
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0205360
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
unable or unwilling to provide informed consent
Beschreibung

Informed Consent Unable | Informed Consent Unwilling

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0558080
currently receiving hcv treatment
Beschreibung

Therapeutic procedure Hepatitis C

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0019196
primary hcv care provider does not agree to their participation in the trial
Beschreibung

Participation Clinical Trial Refused

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C1705116
psychiatrically unstable
Beschreibung

Unstable status Psychiatric

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0443343
UMLS CUI [1,2]
C0205487

Ähnliche Modelle

Eligibility Hepatitis C NCT01442311

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Hepatitis C
Item
hcv-infected
boolean
C0019196 (UMLS CUI [1])
Medical care Hepatitis C Methadone Clinic
Item
receive hcv medical care at the methadone clinic
boolean
C0496675 (UMLS CUI [1,1])
C0019196 (UMLS CUI [1,2])
C1552533 (UMLS CUI [1,3])
Therapeutic procedure Hepatitis C Study Site Planned
Item
plan to initiate hcv treatment on-site within the next 3 months
boolean
C0087111 (UMLS CUI [1,1])
C0019196 (UMLS CUI [1,2])
C2825164 (UMLS CUI [1,3])
C1301732 (UMLS CUI [1,4])
Stable status Psychiatric
Item
psychiatrically stable as determined by hcv treatment provider and/or on-site psychiatrist
boolean
C0205360 (UMLS CUI [1,1])
C0205487 (UMLS CUI [1,2])
Methadone Receive days per week
Item
attend the methadone clinic between three and six days per week to receive methadone
boolean
C0025605 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C0677547 (UMLS CUI [1,3])
Methadone Dose Stable
Item
stable dose fo methadone for two weeks prior to the baseline visit
boolean
C0025605 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Informed Consent Unable | Informed Consent Unwilling
Item
unable or unwilling to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Therapeutic procedure Hepatitis C
Item
currently receiving hcv treatment
boolean
C0087111 (UMLS CUI [1,1])
C0019196 (UMLS CUI [1,2])
Participation Clinical Trial Refused
Item
primary hcv care provider does not agree to their participation in the trial
boolean
C0679823 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C1705116 (UMLS CUI [1,3])
Unstable status Psychiatric
Item
psychiatrically unstable
boolean
C0443343 (UMLS CUI [1,1])
C0205487 (UMLS CUI [1,2])

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