Informatie:
Fout:
ID
30890
Beschrijving
Biomarkers Related to Thrombosis in Patients With Newly Diagnosed Multiple Myeloma Receiving Chemotherapy; ODM derived from: https://clinicaltrials.gov/show/NCT01132833
Link
https://clinicaltrials.gov/show/NCT01132833
Trefwoorden
Versies (1)
- 02-07-18 02-07-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
2 juli 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Multiple Myeloma NCT01132833
Eligibility Multiple Myeloma NCT01132833
- StudyEvent: Eligibility
Similar models
Eligibility Multiple Myeloma NCT01132833
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Recurrent multiple myeloma | Refractory multiple myeloma
Item
newly diagnosed; relapsed, or refractory multiple myeloma
boolean
C1370446 (UMLS CUI [1])
C0278620 (UMLS CUI [2])
C0278620 (UMLS CUI [2])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Central venous access catheter
Item
central venous access devices allowed
boolean
C1145640 (UMLS CUI [1])
Patient Recruitment University Medical Center
Item
recruited by the division of hematology/oncology and the lineberger comprehensive cancer center at the university of north carolina
boolean
C0242800 (UMLS CUI [1,1])
C0000872 (UMLS CUI [1,2])
C0000872 (UMLS CUI [1,2])
Exclusion | Venous Thromboembolism
Item
no history of venous thromboembolism
boolean
C2828389 (UMLS CUI [1])
C1861172 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C1861172 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Exclusion | Hospitalization Duration
Item
no hospitalization for > 2 days within the past month
boolean
C2828389 (UMLS CUI [1])
C0019993 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
C0019993 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
Exclusion | Pregnancy
Item
not pregnant
boolean
C2828389 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
C0032961 (UMLS CUI [2])
Exclusion Criteria | Chemotherapy Refused | Patient Inappropriate Chemotherapy
Item
no patient who refuses or is deemed unsuitable for chemotherapy
boolean
C0680251 (UMLS CUI [1])
C0392920 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
C0030705 (UMLS CUI [3,1])
C1548788 (UMLS CUI [3,2])
C0392920 (UMLS CUI [3,3])
C0392920 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
C0030705 (UMLS CUI [3,1])
C1548788 (UMLS CUI [3,2])
C0392920 (UMLS CUI [3,3])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Exclusion | Operative Surgical Procedures
Item
no surgery within the past month
boolean
C2828389 (UMLS CUI [1])
C0543467 (UMLS CUI [2])
C0543467 (UMLS CUI [2])
Bone marrow biopsy | Central venous line Placement | Biopsy | Fine needle aspiration biopsy
Item
bone marrow biopsies, central venous line placement and diagnostic biopsies by surgery or fine-needle aspiration allowed
boolean
C0005954 (UMLS CUI [1])
C1145640 (UMLS CUI [2,1])
C0021107 (UMLS CUI [2,2])
C0005558 (UMLS CUI [3])
C1510483 (UMLS CUI [4])
C1145640 (UMLS CUI [2,1])
C0021107 (UMLS CUI [2,2])
C0005558 (UMLS CUI [3])
C1510483 (UMLS CUI [4])
Exclusion | Anticoagulation Therapy
Item
* no concurrent anticoagulation therapy
boolean
C2828389 (UMLS CUI [1])
C0003281 (UMLS CUI [2])
C0003281 (UMLS CUI [2])
Antiplatelet Agents | Aspirin | Clopidogrel
Item
concurrent antiplatelet agents, such as aspirin and/or clopidogrel, allowed
boolean
C0085826 (UMLS CUI [1])
C0004057 (UMLS CUI [2])
C0070166 (UMLS CUI [3])
C0004057 (UMLS CUI [2])
C0070166 (UMLS CUI [3])