Central venous catheter for Chemotherapy
Item
Patients receiving a central venous catheter for chemotherapy of AML or ALL
boolean
C1145640 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
Central Venous Catheter Duration
Item
Patients receiving a central venous catheter for high-dose chemotherapy with consecutive autologous stem cell transplantation or any other condition with an expected duration of chemotherapy-associated neutropenia of at least 5 days and an expected duration of central venous catheter use of at least 10 days
boolean
C1145640 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Age
Item
Age >= 18 years
boolean
C0001779 (UMLS CUI [1])
Control Group
Item
Healthy Volunteers
boolean
C0009932 (UMLS CUI [1])
Expected duration of Neutropenia or Central Venous Catheter
Item
Condition with an expected duration of chemotherapy-associated neutropenia of at less than 5 days and an expected duration of central venous catheter use of less than 10 days
boolean
C0449238 (UMLS CUI [1,1])
C1517001 (UMLS CUI [1,2])
C0027947 (UMLS CUI [1,3])
C0449238 (UMLS CUI [2,1])
C1517001 (UMLS CUI [2,2])
C1145640 (UMLS CUI [2,3])
Central Venous Catheter wit antimicrobial coating
Item
Use of a central venous catheter with antimicrobial coating other than chlorhexidine and/or silver-sulfadiazine
boolean
C0180522 (UMLS CUI [1,1])
C1145640 (UMLS CUI [1,2])
Venous status
Item
Limited venous status, impeding acquisition of peripheral blood cultures in case of febrile neutropenia
boolean
C0042449 (UMLS CUI [1])
Study Partricipation Status
Item
Patients previously enrolled in the study
boolean
C2348568 (UMLS CUI [1])
Tunneled central venous catheters
Item
Tunneled central venous catheters
boolean
C0878969 (UMLS CUI [1])
Shaldon catheters
Item
Shaldon catheters
boolean
C0085590 (UMLS CUI [1])
Central Venous Catheter in Femoral vein
Item
CVC insertion via the V. femoralis
boolean
C0085590 (UMLS CUI [1,1])
C0015809 (UMLS CUI [1,2])
Fever
Item
Fever (T > 37.8°C) related to a suspected or confirmed bacterial infection at randomization
boolean
C0015967 (UMLS CUI [1])
Hypersensitivity to Study Drug
Item
Known allergic/hypersensitivity reaction to any compounds of the treatment
boolean
C0020517 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Legal capacity
Item
Legal incapacity or limited legal capacity
boolean
C0683673 (UMLS CUI [1])
Comorbidity, Informed Consent
Item
Medical or psychological condition which in the opinion of the investigator would not permit the patient to complete the study or sign meaningful informed consent
boolean
C0009488 (UMLS CUI [1])
C0021430 (UMLS CUI [2])