ID

21500

Beschreibung

Phase I/II Trial of VELCADE Plus Zevalin in Patients With Relapsed or Refractory Follicular Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00372905

Link

https://clinicaltrials.gov/show/NCT00372905

Stichworte

Versionen (1)
  1. 25.04.17 25.04.17 -
Hochgeladen am

25. April 2017

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0
Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Zurück zu Modell Kommentaren
Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

Eligibility Lymphoma NCT00372905

Englisch

Eligibility Lymphoma NCT00372905

1 Formulare  
  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00372905
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically confirmed follicular lymphoma
Beschreibung

Lymphoma, Follicular

Datentyp

boolean

Alias
UMLS CUI [1]
C0024301
cd20+ at time of diagnosis or subsequently
Beschreibung

CD20 antigen positive

Datentyp

boolean

Alias
UMLS CUI [1]
C3888518
more than 4 weeks since prior rituximab
Beschreibung

rituximab

Datentyp

boolean

Alias
UMLS CUI [1]
C0393022
more than 3 weeks since prior anticancer therapy (6 weeks for nitrosourea or mitomycin c)
Beschreibung

cancer treatment | Nitrosourea | Mitomycin-c

Datentyp

boolean

Alias
UMLS CUI [1]
C0920425
UMLS CUI [2]
C0028210
UMLS CUI [3]
C0002475
more than 4 weeks since prior major surgery
Beschreibung

major surgery

Datentyp

boolean

Alias
UMLS CUI [1]
C0679637
more than 2 weeks since prior investigational drugs
Beschreibung

Investigational New Drugs

Datentyp

boolean

Alias
UMLS CUI [1]
C0013230
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
aids-related lymphoma
Beschreibung

Lymphoma, AIDS-Related

Datentyp

boolean

Alias
UMLS CUI [1]
C0085090
history or evidence of cns involvement
Beschreibung

Central Nervous System Involvement | Central Nervous System Involvement Evidence of

Datentyp

boolean

Alias
UMLS CUI [1]
C4050309
UMLS CUI [2,1]
C4050309
UMLS CUI [2,2]
C0332120
pregnant or nursing
Beschreibung

Pregnancy | Breast Feeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
known hiv positivity
Beschreibung

HIV Seropositivity

Datentyp

boolean

Alias
UMLS CUI [1]
C0019699
serious medical or psychiatric illness that would preclude study participation
Beschreibung

Illness Serious Study Subject Participation Status Exclusion | Mental disorder Serious Study Subject Participation Status Exclusion

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0221423
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C2348568
UMLS CUI [1,4]
C2828389
UMLS CUI [2,1]
C0004936
UMLS CUI [2,2]
C0205404
UMLS CUI [2,3]
C2348568
UMLS CUI [2,4]
C2828389
myocardial infarction within the past 6 months
Beschreibung

Myocardial Infarction

Datentyp

boolean

Alias
UMLS CUI [1]
C0027051
congestive heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or ecg evidence of acute ischemia or active conduction system abnormalities
Beschreibung

Congestive heart failure | Angina control - poor | Ventricular arrhythmia Severe Uncontrolled | Acute myocardial ischemia Evidence Electrocardiography | Conduction system abnormalities

Datentyp

boolean

Alias
UMLS CUI [1]
C0018802
UMLS CUI [2]
C0421196
UMLS CUI [3,1]
C0085612
UMLS CUI [3,2]
C0205082
UMLS CUI [3,3]
C0205318
UMLS CUI [4,1]
C0746731
UMLS CUI [4,2]
C3887511
UMLS CUI [4,3]
C1623258
UMLS CUI [5]
C0151236
known hypersensitivity to rituximab, bortezomib, boron, or mannitol
Beschreibung

Hypersensitivity rituximab | Hypersensitivity bortezomib | Hypersensitivity Boron | Hypersensitivity Mannitol

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0393022
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C1176309
UMLS CUI [3,1]
C0020517
UMLS CUI [3,2]
C0006030
UMLS CUI [4,1]
C0020517
UMLS CUI [4,2]
C0024730
prior autologous or allogeneic stem cell transplantation
Beschreibung

Transplantation of autologous hematopoietic stem cell | Allogeneic Hematopoietic Stem Cell Transplantation

Datentyp

boolean

Alias
UMLS CUI [1]
C1831743
UMLS CUI [2]
C1705576
prior radioimmunoconjugate therapy or prior exposure to murine antibodies
Beschreibung

Radioimmunoconjugates | Murine-Derived Monoclonal Antibodies Exposure to

Datentyp

boolean

Alias
UMLS CUI [1]
C0243019
UMLS CUI [2,1]
C2916903
UMLS CUI [2,2]
C0332157
prior external-beam irradiation to > 25% of active bone marrow
Beschreibung

Teleradiotherapy Bone Marrow Percentage

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0419095
UMLS CUI [1,2]
C0005953
UMLS CUI [1,3]
C0439165
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Lymphoma NCT00372905

1 Formulare
  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00372905
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Lymphoma, Follicular
Item
histologically confirmed follicular lymphoma
boolean
C0024301 (UMLS CUI [1])
CD20 antigen positive
Item
cd20+ at time of diagnosis or subsequently
boolean
C3888518 (UMLS CUI [1])
rituximab
Item
more than 4 weeks since prior rituximab
boolean
C0393022 (UMLS CUI [1])
cancer treatment | Nitrosourea | Mitomycin-c
Item
more than 3 weeks since prior anticancer therapy (6 weeks for nitrosourea or mitomycin c)
boolean
C0920425 (UMLS CUI [1])
C0028210 (UMLS CUI [2])
C0002475 (UMLS CUI [3])
major surgery
Item
more than 4 weeks since prior major surgery
boolean
C0679637 (UMLS CUI [1])
Investigational New Drugs
Item
more than 2 weeks since prior investigational drugs
boolean
C0013230 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Lymphoma, AIDS-Related
Item
aids-related lymphoma
boolean
C0085090 (UMLS CUI [1])
Central Nervous System Involvement | Central Nervous System Involvement Evidence of
Item
history or evidence of cns involvement
boolean
C4050309 (UMLS CUI [1])
C4050309 (UMLS CUI [2,1])
C0332120 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
HIV Seropositivity
Item
known hiv positivity
boolean
C0019699 (UMLS CUI [1])
Illness Serious Study Subject Participation Status Exclusion | Mental disorder Serious Study Subject Participation Status Exclusion
Item
serious medical or psychiatric illness that would preclude study participation
boolean
C0221423 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
C2828389 (UMLS CUI [1,4])
C0004936 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C2348568 (UMLS CUI [2,3])
C2828389 (UMLS CUI [2,4])
Myocardial Infarction
Item
myocardial infarction within the past 6 months
boolean
C0027051 (UMLS CUI [1])
Congestive heart failure | Angina control - poor | Ventricular arrhythmia Severe Uncontrolled | Acute myocardial ischemia Evidence Electrocardiography | Conduction system abnormalities
Item
congestive heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or ecg evidence of acute ischemia or active conduction system abnormalities
boolean
C0018802 (UMLS CUI [1])
C0421196 (UMLS CUI [2])
C0085612 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0205318 (UMLS CUI [3,3])
C0746731 (UMLS CUI [4,1])
C3887511 (UMLS CUI [4,2])
C1623258 (UMLS CUI [4,3])
C0151236 (UMLS CUI [5])
Hypersensitivity rituximab | Hypersensitivity bortezomib | Hypersensitivity Boron | Hypersensitivity Mannitol
Item
known hypersensitivity to rituximab, bortezomib, boron, or mannitol
boolean
C0020517 (UMLS CUI [1,1])
C0393022 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C1176309 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0006030 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C0024730 (UMLS CUI [4,2])
Transplantation of autologous hematopoietic stem cell | Allogeneic Hematopoietic Stem Cell Transplantation
Item
prior autologous or allogeneic stem cell transplantation
boolean
C1831743 (UMLS CUI [1])
C1705576 (UMLS CUI [2])
Radioimmunoconjugates | Murine-Derived Monoclonal Antibodies Exposure to
Item
prior radioimmunoconjugate therapy or prior exposure to murine antibodies
boolean
C0243019 (UMLS CUI [1])
C2916903 (UMLS CUI [2,1])
C0332157 (UMLS CUI [2,2])
Teleradiotherapy Bone Marrow Percentage
Item
prior external-beam irradiation to > 25% of active bone marrow
boolean
C0419095 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
C0439165 (UMLS CUI [1,3])
Zum Seitenanfang zurückkehren 

Kontakt

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Hilfe

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video