Informed Consent
Item
patient is willing and able to give informed consent for participation in the trial.
boolean
C0021430 (UMLS CUI [1])
Age | Chronic haemodialysis Therapeutic procedure | Life Expectancy
Item
male or female, aged 18 years to 70 yrs. undergoing chronic hemodialysis treatment for more than 3 months (life expectancy > 1 year).
boolean
C0001779 (UMLS CUI [1])
C1740835 (UMLS CUI [2,1])
C0087111 (UMLS CUI [2,2])
C0023671 (UMLS CUI [3])
Compliance behavior Study Protocol
Item
able and willing to comply with all trial requirements.
boolean
C1321605 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
Study Subject Participation Status
Item
willing to allow his or her /physician/nephrologist/general practitioner and consultant, if appropriate, to be notified of participation in the trial.
boolean
C2348568 (UMLS CUI [1])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
participants who have participated in another research trial involving an investigational product in the past 12 weeks.
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
Kidney Transplantation Functional | Live donor renal transplant
Item
history of functional kidney transplant 6 months before study entry; anticipated live donor kidney transplant over the study duration;
boolean
C0022671 (UMLS CUI [1,1])
C0205245 (UMLS CUI [1,2])
C0401177 (UMLS CUI [2])
Vitamin E Containing Supplement
Item
participants who are taking vitamin e- containing supplements >60 iu/d during the past 30 days
boolean
C0042874 (UMLS CUI [1,1])
C0332256 (UMLS CUI [1,2])
C2348609 (UMLS CUI [1,3])
Compliance behavior Hemodialysis | Compliance behavior to medical regimen
Item
history of poor adherence to hemodialysis or medical regimen
boolean
C1321605 (UMLS CUI [1,1])
C0019004 (UMLS CUI [1,2])
C4039237 (UMLS CUI [2])
cancer treatment | Basal cell carcinoma
Item
participants who are currently on active treatment for cancer, excluding basal cell carcinoma of the skin
boolean
C0920425 (UMLS CUI [1])
C0007117 (UMLS CUI [2])
HIV | Acquired Immunodeficiency Syndrome | Anti-HIV Therapy | HIV Seropositivity
Item
participants who have been diagnosed as hiv/aids and/or on the anti-hiv therapy. (hiv seropositivity is not an exclusion criterion)
boolean
C0019682 (UMLS CUI [1])
C0001175 (UMLS CUI [2])
C1510425 (UMLS CUI [3])
C0019699 (UMLS CUI [4])
Anti-Inflammatory Agents | Aspirin
Item
patients taking anti-inflammatory medication, except aspirin<325 mg/d, over the past 30 days
boolean
C0003209 (UMLS CUI [1])
C0004057 (UMLS CUI [2])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
female participant who is pregnant, lactating or planning pregnancy during the course of the trial
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Enteral nutritional support | Nutritional Support Intravenous
Item
participants who are receiving nutritional support (i.e. enteral and intra-venous route)
boolean
C0846670 (UMLS CUI [1])
C0242739 (UMLS CUI [2,1])
C0348016 (UMLS CUI [2,2])
catheter Dialysis | Graft
Item
patients using a temporary catheter for dialysis access at baseline or patients receiving a graft/fistula within the 6-month study period
boolean
C0085590 (UMLS CUI [1,1])
C0011946 (UMLS CUI [1,2])
C0181074 (UMLS CUI [2])
Hospitalization
Item
more than two hospitalizations within the last 90 days or one hospitalization within the 30 days preceding enrollment
boolean
C0019993 (UMLS CUI [1])
Comorbidity Risk Study Subject | Comorbidity Affecting research results | Comorbidity Study Subject Participation Status Limited
Item
any other significant disease or disorder which, in the opinion of their nephrologist, may either put the participants at risk because of participation in the trial, or may influence the result of the trial, or the participant's ability to participate in the trial.
boolean
C0009488 (UMLS CUI [1,1])
C0035647 (UMLS CUI [1,2])
C0681850 (UMLS CUI [1,3])
C0009488 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C0683954 (UMLS CUI [2,3])
C0009488 (UMLS CUI [3,1])
C2348568 (UMLS CUI [3,2])
C0439801 (UMLS CUI [3,3])