Información:
Error:
ID
31398
Descripción
A Pharmacokinetic Study of Subcutaneous and Intravenous MabThera (Rituximab) in Patients With Follicular Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00930514
Link
https://clinicaltrials.gov/show/NCT00930514
Palabras clave
Versiones (1)
- 19/8/18 19/8/18 -
Titular de derechos de autor
see clinicaltrials.gov
Subido en
19 de agosto de 2018
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 Lymphoma, Follicular NCT00930514
Eligibility Lymphoma, Follicular NCT00930514
- StudyEvent: Eligibility
Similar models
Eligibility Lymphoma, Follicular NCT00930514
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Age
Item
adult patients, >=18 years of age;
boolean
C0001779 (UMLS CUI [1])
Lymphoma, Non-Hodgkin; Lymphoma, Follicular; CD20 antigen positive
Item
cd20-positive follicular non-hodgkin's lymphoma (nhl);
boolean
C0024305 (UMLS CUI [1,1])
C0024301 (UMLS CUI [1,2])
C3888518 (UMLS CUI [1,3])
C0024301 (UMLS CUI [1,2])
C3888518 (UMLS CUI [1,3])
partial response | Complete therapeutic response | Induction Chemotherapy; Mabthera
Item
partial or complete response a the end of induction treatment with mabthera;
boolean
C1521726 (UMLS CUI [1])
C1275810 (UMLS CUI [2])
C3179010 (UMLS CUI [3,1])
C1314901 (UMLS CUI [3,2])
C1275810 (UMLS CUI [2])
C3179010 (UMLS CUI [3,1])
C1314901 (UMLS CUI [3,2])
Induction Chemotherapy; Complete | Maintenance therapy; Mabthera; Intravenous
Item
must have completed induction treatment, and received >= 1 dose of iv mabthera maintenance treatment;
boolean
C3179010 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0677908 (UMLS CUI [2,1])
C1314901 (UMLS CUI [2,2])
C0348016 (UMLS CUI [2,3])
C0205197 (UMLS CUI [1,2])
C0677908 (UMLS CUI [2,1])
C1314901 (UMLS CUI [2,2])
C0348016 (UMLS CUI [2,3])
ECOG performance status
Item
ecog performance status of <=2.
boolean
C1520224 (UMLS CUI [1])
Lymphoma, Non-Hodgkin; cell transformation | Lymphoma, Follicular
Item
histological evidence of transformation of nhl, or types of nhl other than follicular lymphoma;
boolean
C0024305 (UMLS CUI [1,1])
C0040682 (UMLS CUI [1,2])
C0024301 (UMLS CUI [2])
C0040682 (UMLS CUI [1,2])
C0024301 (UMLS CUI [2])
CNS disorder
Item
presence or history of cns disease;
boolean
C0007682 (UMLS CUI [1])
Malignant Neoplasms | Lymphoma, Non-Hodgkin; Lymphoma, Follicular | Protocol Compliance | Interpretation of results
Item
history of malignancy other than follicular nhl which could affect compliance with protocol or interpretation of results;
boolean
C0006826 (UMLS CUI [1])
C0024305 (UMLS CUI [2,1])
C0024301 (UMLS CUI [2,2])
C0525058 (UMLS CUI [3])
C3526596 (UMLS CUI [4])
C0024305 (UMLS CUI [2,1])
C0024301 (UMLS CUI [2,2])
C0525058 (UMLS CUI [3])
C3526596 (UMLS CUI [4])
major surgery; Time | Biopsy of lymph node; Exclude
Item
recent major surgery (within 4 weeks prior to screening, excluding lymph node biopsy).
boolean
C0679637 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C0193842 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0040223 (UMLS CUI [1,2])
C0193842 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])