ID

27887

Descripción

The Effects of Adding TCM-700C on the Standard Combination Treatment for Patients With Genotype 1 Hepatitis C Infection; ODM derived from: https://clinicaltrials.gov/show/NCT00556504

Link

https://clinicaltrials.gov/show/NCT00556504

Palabras clave

  1. 4/12/17 4/12/17 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

4 de diciembre de 2017

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0

Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Chronic Hepatitis C NCT00556504

Eligibility Chronic Hepatitis C NCT00556504

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
hcv strain confirmed as genotype i;
Descripción

Hepatitis C virus genotype 1

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3532919
elevated alt (≥1.5 x upper limit of normal)during last 6 months
Descripción

Alanine aminotransferase increased

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0151905
females of childbearing potential with a negative serum pregnancy test
Descripción

Childbearing Potential Serum pregnancy test negative

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0430061
subject must be willing to sign a written informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
subject must be willing and able to adhere to dose and visit schedule.
Descripción

Protocol Compliance

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0525058
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
serum afp levels > 400 ng/ml
Descripción

serum alpha-fetoprotein (AFP) measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0546833
liver biopsy within 12 months prior to study entry showed liver cirrhosis with metavir system fibrosis score of 3-4, or hepatocellular carcinoma (hcc);
Descripción

Liver Cirrhosis METAVIR Fibrosis Score Biopsy of liver | Liver carcinoma

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0023890
UMLS CUI [1,2]
C3897040
UMLS CUI [1,3]
C0193388
UMLS CUI [2]
C2239176
co-infection with hepatitis b virus (hbv);
Descripción

HBV coinfection

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2242656
anti-hiv positive;
Descripción

HIV antibody positive

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0920548

Similar models

Eligibility Chronic Hepatitis C NCT00556504

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Hepatitis C virus genotype 1
Item
hcv strain confirmed as genotype i;
boolean
C3532919 (UMLS CUI [1])
Alanine aminotransferase increased
Item
elevated alt (≥1.5 x upper limit of normal)during last 6 months
boolean
C0151905 (UMLS CUI [1])
Childbearing Potential Serum pregnancy test negative
Item
females of childbearing potential with a negative serum pregnancy test
boolean
C3831118 (UMLS CUI [1,1])
C0430061 (UMLS CUI [1,2])
Informed Consent
Item
subject must be willing to sign a written informed consent
boolean
C0021430 (UMLS CUI [1])
Protocol Compliance
Item
subject must be willing and able to adhere to dose and visit schedule.
boolean
C0525058 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
serum alpha-fetoprotein (AFP) measurement
Item
serum afp levels > 400 ng/ml
boolean
C0546833 (UMLS CUI [1])
Liver Cirrhosis METAVIR Fibrosis Score Biopsy of liver | Liver carcinoma
Item
liver biopsy within 12 months prior to study entry showed liver cirrhosis with metavir system fibrosis score of 3-4, or hepatocellular carcinoma (hcc);
boolean
C0023890 (UMLS CUI [1,1])
C3897040 (UMLS CUI [1,2])
C0193388 (UMLS CUI [1,3])
C2239176 (UMLS CUI [2])
HBV coinfection
Item
co-infection with hepatitis b virus (hbv);
boolean
C2242656 (UMLS CUI [1])
HIV antibody positive
Item
anti-hiv positive;
boolean
C0920548 (UMLS CUI [1])

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial