ID

39153

Beschrijving

Pomegranate and Hemodialysis Pilot Trial; ODM derived from: https://clinicaltrials.gov/show/NCT01562340

Link

https://clinicaltrials.gov/show/NCT01562340

Trefwoorden

Versies (2)
  1. 05-12-19 05-12-19 -
  2. 05-12-19 05-12-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

5 december 2019

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility End Stage Renal Disease NCT01562340

Engels

Eligibility End Stage Renal Disease NCT01562340

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with end-stage renal disease receiving thrice weekly hemodialysis
Beschrijving

Kidney Failure, Chronic | Hemodialysis times per week

Datatype

boolean

Alias
UMLS CUI [1]
C0022661
UMLS CUI [2,1]
C0019004
UMLS CUI [2,2]
C0456698
age > 18 or < 85 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
life expectancy greater than one year
Beschrijving

Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
ability to understand and provide informed consent for participation in the study
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of poor adherence to hemodialysis or medical regimen
Beschrijving

Adherence Poor Hemodialysis | Adherence Poor Regimen

Datatype

boolean

Alias
UMLS CUI [1,1]
C1510802
UMLS CUI [1,2]
C0542537
UMLS CUI [1,3]
C0019004
UMLS CUI [2,1]
C1510802
UMLS CUI [2,2]
C0542537
UMLS CUI [2,3]
C0040808
prisoners, patients with significant mental illness, and other vulnerable populations
Beschrijving

Prisoners | Mental disorders | Vulnerable Populations

Datatype

boolean

Alias
UMLS CUI [1]
C0033167
UMLS CUI [2]
C0004936
UMLS CUI [3]
C0949366
aids (hiv seropositivity is not an exclusion criteria)
Beschrijving

AIDS | HIV Seropositivity allowed

Datatype

boolean

Alias
UMLS CUI [1]
C0001175
UMLS CUI [2,1]
C0019699
UMLS CUI [2,2]
C0683607
active malignancy excluding basal cell carcinoma of the skin
Beschrijving

Malignant Neoplasms | Exception Basal cell carcinoma

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0007117
gastrointestinal dysfunction requiring parenteral nutrition
Beschrijving

Gastrointestinal dysfunction Requirement Parenteral Nutrition

Datatype

boolean

Alias
UMLS CUI [1,1]
C0679407
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0030547
history of functional kidney transplant < 6 months prior to study entry
Beschrijving

Kidney Transplantation Functional

Datatype

boolean

Alias
UMLS CUI [1,1]
C0022671
UMLS CUI [1,2]
C0205245
anticipated live donor kidney transplant
Beschrijving

Live donor renal transplant Anticipated

Datatype

boolean

Alias
UMLS CUI [1,1]
C0401177
UMLS CUI [1,2]
C3840775
patients taking vitamin e supplements > 60 iu/day, vitamin c > 150 mg/day or other antioxidant or nutritional supplements
Beschrijving

Vitamin E supplement IU/day | Vitamin C mg/day | Antioxidant Supplements | Nutritional Supplements

Datatype

boolean

Alias
UMLS CUI [1,1]
C3661607
UMLS CUI [1,2]
C0439465
UMLS CUI [2,1]
C0003968
UMLS CUI [2,2]
C0439422
UMLS CUI [3,1]
C0003402
UMLS CUI [3,2]
C0242295
UMLS CUI [4]
C0242295
incident hemodialysis patients (defined as within 30 days of dialysis initiation)
Beschrijving

Hemodialysis Initiation Timespan

Datatype

boolean

Alias
UMLS CUI [1,1]
C0019004
UMLS CUI [1,2]
C1704686
UMLS CUI [1,3]
C0872291
patients hospitalized for more than 5 days within the past 30 days.
Beschrijving

Hospitalization Duration

Datatype

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0449238
patients with a history of a major atherosclerotic event (defined as combined incidence of myocardial infarction, urgent target-vessel revascularization, coronary bypass surgery, and stroke) within three months
Beschrijving

Event atherosclerotic major | Incidence Combined | Myocardial Infarction | Target vessel Revascularization Urgent | Coronary Artery Bypass Surgery | Cerebrovascular accident

Datatype

boolean

Alias
UMLS CUI [1,1]
C0441471
UMLS CUI [1,2]
C0333482
UMLS CUI [1,3]
C0205164
UMLS CUI [2,1]
C0021149
UMLS CUI [2,2]
C0205195
UMLS CUI [3]
C0027051
UMLS CUI [4,1]
C0449618
UMLS CUI [4,2]
C0581603
UMLS CUI [4,3]
C0439609
UMLS CUI [5]
C0010055
UMLS CUI [6]
C0038454
pregnancy
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
Terug naar het begin van de pagina

Similar models

Eligibility End Stage Renal Disease NCT01562340

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Kidney Failure, Chronic | Hemodialysis times per week
Item
patients with end-stage renal disease receiving thrice weekly hemodialysis
boolean
C0022661 (UMLS CUI [1])
C0019004 (UMLS CUI [2,1])
C0456698 (UMLS CUI [2,2])
Age
Item
age > 18 or < 85 years
boolean
C0001779 (UMLS CUI [1])
Life Expectancy
Item
life expectancy greater than one year
boolean
C0023671 (UMLS CUI [1])
Informed Consent
Item
ability to understand and provide informed consent for participation in the study
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Adherence Poor Hemodialysis | Adherence Poor Regimen
Item
history of poor adherence to hemodialysis or medical regimen
boolean
C1510802 (UMLS CUI [1,1])
C0542537 (UMLS CUI [1,2])
C0019004 (UMLS CUI [1,3])
C1510802 (UMLS CUI [2,1])
C0542537 (UMLS CUI [2,2])
C0040808 (UMLS CUI [2,3])
Prisoners | Mental disorders | Vulnerable Populations
Item
prisoners, patients with significant mental illness, and other vulnerable populations
boolean
C0033167 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
C0949366 (UMLS CUI [3])
AIDS | HIV Seropositivity allowed
Item
aids (hiv seropositivity is not an exclusion criteria)
boolean
C0001175 (UMLS CUI [1])
C0019699 (UMLS CUI [2,1])
C0683607 (UMLS CUI [2,2])
Malignant Neoplasms | Exception Basal cell carcinoma
Item
active malignancy excluding basal cell carcinoma of the skin
boolean
C0006826 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0007117 (UMLS CUI [2,2])
Gastrointestinal dysfunction Requirement Parenteral Nutrition
Item
gastrointestinal dysfunction requiring parenteral nutrition
boolean
C0679407 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0030547 (UMLS CUI [1,3])
Kidney Transplantation Functional
Item
history of functional kidney transplant < 6 months prior to study entry
boolean
C0022671 (UMLS CUI [1,1])
C0205245 (UMLS CUI [1,2])
Live donor renal transplant Anticipated
Item
anticipated live donor kidney transplant
boolean
C0401177 (UMLS CUI [1,1])
C3840775 (UMLS CUI [1,2])
Vitamin E supplement IU/day | Vitamin C mg/day | Antioxidant Supplements | Nutritional Supplements
Item
patients taking vitamin e supplements > 60 iu/day, vitamin c > 150 mg/day or other antioxidant or nutritional supplements
boolean
C3661607 (UMLS CUI [1,1])
C0439465 (UMLS CUI [1,2])
C0003968 (UMLS CUI [2,1])
C0439422 (UMLS CUI [2,2])
C0003402 (UMLS CUI [3,1])
C0242295 (UMLS CUI [3,2])
C0242295 (UMLS CUI [4])
Hemodialysis Initiation Timespan
Item
incident hemodialysis patients (defined as within 30 days of dialysis initiation)
boolean
C0019004 (UMLS CUI [1,1])
C1704686 (UMLS CUI [1,2])
C0872291 (UMLS CUI [1,3])
Hospitalization Duration
Item
patients hospitalized for more than 5 days within the past 30 days.
boolean
C0019993 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Event atherosclerotic major | Incidence Combined | Myocardial Infarction | Target vessel Revascularization Urgent | Coronary Artery Bypass Surgery | Cerebrovascular accident
Item
patients with a history of a major atherosclerotic event (defined as combined incidence of myocardial infarction, urgent target-vessel revascularization, coronary bypass surgery, and stroke) within three months
boolean
C0441471 (UMLS CUI [1,1])
C0333482 (UMLS CUI [1,2])
C0205164 (UMLS CUI [1,3])
C0021149 (UMLS CUI [2,1])
C0205195 (UMLS CUI [2,2])
C0027051 (UMLS CUI [3])
C0449618 (UMLS CUI [4,1])
C0581603 (UMLS CUI [4,2])
C0439609 (UMLS CUI [4,3])
C0010055 (UMLS CUI [5])
C0038454 (UMLS CUI [6])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial