ID

27386

Descripción

Imiquimod 5% Cream for the Treatment of Periocular Basal Cell Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00803907

Link

https://clinicaltrials.gov/show/NCT00803907

Palabras clave

Versiones (1)
  1. 11-11-17 11-11-17 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

11 november 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.

Volver a los comentarios del modelo
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 Carcinoma, Basal Cell NCT00803907

Inglés

Eligibility Carcinoma, Basal Cell NCT00803907

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients whose injuries were confirmed by anatomical and pathological study (periocular superficial basal cell carcinoma).
Descripción

Superficial basal cell carcinoma Periocular

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0862889
UMLS CUI [1,2]
C0230064
patients with clinical counter indication for reconstructive surgery (high surgical risk).
Descripción

Medical contraindication Reconstructive Surgical Procedures | Medical contraindication Operative Surgical Procedures High risk

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0524865
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0543467
UMLS CUI [2,3]
C0332167
patients who have refused a restorative surgery. (aesthetic reasons)
Descripción

Reconstructive Surgical Procedures Refused

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0524865
UMLS CUI [1,2]
C1705116
patients who have signed the free and informed consent.
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who have a hypersensitivity reaction to the formula components.
Descripción

Hypersensitivity Pharmaceutical Formulation Component

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1705957
UMLS CUI [1,3]
C1705248
children under 12 years of age.
Descripción

Child | Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0008059
UMLS CUI [2]
C0001779
pregnant and breastfeeding women.
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients whose injury was not confirmed by anatomical and pathological study.
Descripción

Injury Confirmation Lacking

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3263722
UMLS CUI [1,2]
C0750484
UMLS CUI [1,3]
C0332268
individuals with previous autoimmune or inflammatory disease.
Descripción

Autoimmune Disease | Inflammatory disorder

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004364
UMLS CUI [2]
C1290884
patients who have refused to sign the free and informed term of consent.
Descripción

Informed Consent Refused

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1705116
Volver a la parte superior de la página

Similar models

Eligibility Carcinoma, Basal Cell NCT00803907

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Superficial basal cell carcinoma Periocular
Item
patients whose injuries were confirmed by anatomical and pathological study (periocular superficial basal cell carcinoma).
boolean
C0862889 (UMLS CUI [1,1])
C0230064 (UMLS CUI [1,2])
Medical contraindication Reconstructive Surgical Procedures | Medical contraindication Operative Surgical Procedures High risk
Item
patients with clinical counter indication for reconstructive surgery (high surgical risk).
boolean
C1301624 (UMLS CUI [1,1])
C0524865 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0543467 (UMLS CUI [2,2])
C0332167 (UMLS CUI [2,3])
Reconstructive Surgical Procedures Refused
Item
patients who have refused a restorative surgery. (aesthetic reasons)
boolean
C0524865 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])
Informed Consent
Item
patients who have signed the free and informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Hypersensitivity Pharmaceutical Formulation Component
Item
patients who have a hypersensitivity reaction to the formula components.
boolean
C0020517 (UMLS CUI [1,1])
C1705957 (UMLS CUI [1,2])
C1705248 (UMLS CUI [1,3])
Child | Age
Item
children under 12 years of age.
boolean
C0008059 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnant and breastfeeding women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Injury Confirmation Lacking
Item
patients whose injury was not confirmed by anatomical and pathological study.
boolean
C3263722 (UMLS CUI [1,1])
C0750484 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Autoimmune Disease | Inflammatory disorder
Item
individuals with previous autoimmune or inflammatory disease.
boolean
C0004364 (UMLS CUI [1])
C1290884 (UMLS CUI [2])
Informed Consent Refused
Item
patients who have refused to sign the free and informed term of consent.
boolean
C0021430 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

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