ID

22440

Beschreibung

ODM derived from http://clinicaltrials.gov/show/NCT00185393

Link

http://clinicaltrials.gov/show/NCT00185393

Stichworte

  1. 09.12.11 09.12.11 -
  2. 04.06.17 04.06.17 - Martin Dugas
Hochgeladen am

4. Juni 2017

DOI

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Lizenz

Creative Commons BY 4.0

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Treatment With [90]Y-Ibritumomab Tiuxetan Versus no Treatment in Patients With Follicular Non Hodgkin Lymphoma (Stage III or IV) Having Achieved a Partial or Complete Remission After First Line Chemotherapy

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
18 Years and older
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
Non Hodgkin Lymphoma stage III or IV at timepoint of diagnosis
Beschreibung

NHL III/IV

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0024305
UMLS CUI [1,2]
C0280116
UMLS CUI [1,3]
C0280117
Patients who have achieved a remission after first line chemotherapy
Beschreibung

remission after first line chemotherapy

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0687702
UMLS CUI [1,2]
C2045825
No less than 6 weeks and no more than 12 weeks since last dose of chemotherapy
Beschreibung

6-12 weeks since last dose of chemotherapy

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1531781
UMLS CUI [1,2]
C1442456
written informed consent
Beschreibung

consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Any other anticancer treatment for NHL except the preceding first line chemotherapy
Beschreibung

other anticancer treatment

Datentyp

boolean

Alias
UMLS CUI [1]
C0478584
Prior radiation therapy
Beschreibung

Prior radiation therapy

Datentyp

boolean

Alias
UMLS CUI [1]
C0279134
Patients who have not recovered from the toxic effects of the first line chemotherapy
Beschreibung

no recovery from chemotherapy

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1709277
UMLS CUI [1,2]
C0392920
Any other cancer or history of cancer less than 10 years ago
Beschreibung

other cancer

Datentyp

boolean

Alias
UMLS CUI [1]
C1707251
Patients with known HIV positivity
Beschreibung

HIV

Datentyp

boolean

Alias
UMLS CUI [1]
C0019682
patients with pleural effusion or ascites
Beschreibung

pleural effusion or ascites

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0032227
UMLS CUI [1,2]
C0003962
female patients who are pregnant or breast feeding (women of childbearing potential must have a negative serum pregnancy test at study entry)
Beschreibung

pregnant or breast feeding

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
Adults not employing an effective method of birth control during study treatment and 12 months thereafter
Beschreibung

no contraception

Datentyp

boolean

Alias
UMLS CUI [1]
C2919192
Patients unable or unwilling to comply with protocol
Beschreibung

non-compliance

Datentyp

boolean

Alias
UMLS CUI [1]
C0457432

Ähnliche Modelle

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
Age
Item
18 Years and older
boolean
C0001779 (UMLS CUI [1])
NHL III/IV
Item
Non Hodgkin Lymphoma stage III or IV at timepoint of diagnosis
boolean
C0024305 (UMLS CUI [1,1])
C0280116 (UMLS CUI [1,2])
C0280117 (UMLS CUI [1,3])
remission after first line chemotherapy
Item
Patients who have achieved a remission after first line chemotherapy
boolean
C0687702 (UMLS CUI [1,1])
C2045825 (UMLS CUI [1,2])
6-12 weeks since last dose of chemotherapy
Item
No less than 6 weeks and no more than 12 weeks since last dose of chemotherapy
boolean
C1531781 (UMLS CUI [1,1])
C1442456 (UMLS CUI [1,2])
consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
other anticancer treatment
Item
Any other anticancer treatment for NHL except the preceding first line chemotherapy
boolean
C0478584 (UMLS CUI [1])
Prior radiation therapy
Item
Prior radiation therapy
boolean
C0279134 (UMLS CUI [1])
no recovery from chemotherapy
Item
Patients who have not recovered from the toxic effects of the first line chemotherapy
boolean
C1709277 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
other cancer
Item
Any other cancer or history of cancer less than 10 years ago
boolean
C1707251 (UMLS CUI [1])
HIV
Item
Patients with known HIV positivity
boolean
C0019682 (UMLS CUI [1])
pleural effusion or ascites
Item
patients with pleural effusion or ascites
boolean
C0032227 (UMLS CUI [1,1])
C0003962 (UMLS CUI [1,2])
pregnant or breast feeding
Item
female patients who are pregnant or breast feeding (women of childbearing potential must have a negative serum pregnancy test at study entry)
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
no contraception
Item
Adults not employing an effective method of birth control during study treatment and 12 months thereafter
boolean
C2919192 (UMLS CUI [1])
non-compliance
Item
Patients unable or unwilling to comply with protocol
boolean
C0457432 (UMLS CUI [1])

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