Information:
Error:
ID
22440
Description
ODM derived from http://clinicaltrials.gov/show/NCT00185393
Link
http://clinicaltrials.gov/show/NCT00185393
Keywords
Versions (2)
- 12/9/11 12/9/11 -
- 6/4/17 6/4/17 - Martin Dugas
Uploaded on
June 4, 2017
DOI
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License
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
Similar models
Eligibility
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
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])
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])
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])
C1442456 (UMLS CUI [1,2])
consent
Item
written informed consent
boolean
C0021430 (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])
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])
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])
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])