ID

39155

Beskrivning

Evaluation of Daily HemoDialysis at Low Dialysate Flow in Patients Previously Treated With Conventional Hemodialysis; ODM derived from: https://clinicaltrials.gov/show/NCT01845012

Länk

https://clinicaltrials.gov/show/NCT01845012

Nyckelord

Versioner (1)
  1. 2019-12-05 2019-12-05 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

5 december 2019

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0
Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Tillbaka till modellkommentarer
Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility End Stage Renal Disease NCT01845012

Engelsk

Eligibility End Stage Renal Disease NCT01845012

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
age ≥ 18 years
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
patients who give voluntary signed informed consent
Beskrivning

Informed Consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
patients affiliated with the french universal health care system or similar
Beskrivning

Patients Affiliated Health Care System

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1510825
UMLS CUI [1,3]
C0018696
for women of childbearing potential: serum or urine negative pregnancy test
Beskrivning

Childbearing Potential Serum pregnancy test negative | Childbearing Potential Urine pregnancy test negative

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0430061
UMLS CUI [2,1]
C3831118
UMLS CUI [2,2]
C0430057
patients treated with conventional hemodialysis (3 times 4h to 5h per week at at least a dialysate flow rate of 500 ml/min) for at least 3 months and clinically stable (investigator assessment)
Beskrivning

Hemodialysis times per week | Dialysate Flow Rate

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0019004
UMLS CUI [1,2]
C0456698
UMLS CUI [2,1]
C0011947
UMLS CUI [2,2]
C2826285
bipuncture patients (or with double lumen central venous catheter) with stable vascular access and easy to puncture
Beskrivning

Puncture of vessel | Central venous catheter Double lumen | Vascular access Stable

Datatyp

boolean

Alias
UMLS CUI [1]
C0176672
UMLS CUI [2,1]
C1145640
UMLS CUI [2,2]
C0441131
UMLS CUI [3,1]
C0750138
UMLS CUI [3,2]
C0205360
patients willing to be treated with daily hemodialysis at low dialysate flow during the study period (6 times 2h to 2h30 per week at a dialysate flow rate of 200 ml/min in order that the total duration of weekly dialysis is equivalent to the duration of weekly dialysis during the last 3 months of conventional hemodialysis)
Beskrivning

Hemodialysis Daily | Dialysate Flow Rate low

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0019004
UMLS CUI [1,2]
C0332173
UMLS CUI [2,1]
C0011947
UMLS CUI [2,2]
C2826285
UMLS CUI [2,3]
C0205251
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant women or women who could become pregnant during the study (planned pregnancy within 3 months)
Beskrivning

Pregnancy | Pregnancy, Planned

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
patients not affiliated with the french universal health care system
Beskrivning

Affiliation Health Care System Lacking

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1510825
UMLS CUI [1,2]
C0018696
UMLS CUI [1,3]
C0332268
minor patients
Beskrivning

Minor Patients

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0026193
UMLS CUI [1,2]
C0030705
patients who are protected adults according to the terms of the law (french public health laws).
Beskrivning

Protection of patient Law

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0412786
UMLS CUI [1,2]
C0220866
refusal to give consent
Beskrivning

Informed Consent Refused

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1705116
patients simultaneously participating in another trial that may interfere with the study results
Beskrivning

Study Subject Participation Status | Interference Research results

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0521102
UMLS CUI [2,2]
C0683954
Tillbaka till toppen

Similar models

Eligibility End Stage Renal Disease NCT01845012

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age ≥ 18 years
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
patients who give voluntary signed informed consent
boolean
C0021430 (UMLS CUI [1])
Patients Affiliated Health Care System
Item
patients affiliated with the french universal health care system or similar
boolean
C0030705 (UMLS CUI [1,1])
C1510825 (UMLS CUI [1,2])
C0018696 (UMLS CUI [1,3])
Childbearing Potential Serum pregnancy test negative | Childbearing Potential Urine pregnancy test negative
Item
for women of childbearing potential: serum or urine negative pregnancy test
boolean
C3831118 (UMLS CUI [1,1])
C0430061 (UMLS CUI [1,2])
C3831118 (UMLS CUI [2,1])
C0430057 (UMLS CUI [2,2])
Hemodialysis times per week | Dialysate Flow Rate
Item
patients treated with conventional hemodialysis (3 times 4h to 5h per week at at least a dialysate flow rate of 500 ml/min) for at least 3 months and clinically stable (investigator assessment)
boolean
C0019004 (UMLS CUI [1,1])
C0456698 (UMLS CUI [1,2])
C0011947 (UMLS CUI [2,1])
C2826285 (UMLS CUI [2,2])
Puncture of vessel | Central venous catheter Double lumen | Vascular access Stable
Item
bipuncture patients (or with double lumen central venous catheter) with stable vascular access and easy to puncture
boolean
C0176672 (UMLS CUI [1])
C1145640 (UMLS CUI [2,1])
C0441131 (UMLS CUI [2,2])
C0750138 (UMLS CUI [3,1])
C0205360 (UMLS CUI [3,2])
Hemodialysis Daily | Dialysate Flow Rate low
Item
patients willing to be treated with daily hemodialysis at low dialysate flow during the study period (6 times 2h to 2h30 per week at a dialysate flow rate of 200 ml/min in order that the total duration of weekly dialysis is equivalent to the duration of weekly dialysis during the last 3 months of conventional hemodialysis)
boolean
C0019004 (UMLS CUI [1,1])
C0332173 (UMLS CUI [1,2])
C0011947 (UMLS CUI [2,1])
C2826285 (UMLS CUI [2,2])
C0205251 (UMLS CUI [2,3])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Pregnancy, Planned
Item
pregnant women or women who could become pregnant during the study (planned pregnancy within 3 months)
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Affiliation Health Care System Lacking
Item
patients not affiliated with the french universal health care system
boolean
C1510825 (UMLS CUI [1,1])
C0018696 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Minor Patients
Item
minor patients
boolean
C0026193 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
Protection of patient Law
Item
patients who are protected adults according to the terms of the law (french public health laws).
boolean
C0412786 (UMLS CUI [1,1])
C0220866 (UMLS CUI [1,2])
Informed Consent Refused
Item
refusal to give consent
boolean
C0021430 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])
Study Subject Participation Status | Interference Research results
Item
patients simultaneously participating in another trial that may interfere with the study results
boolean
C2348568 (UMLS CUI [1])
C0521102 (UMLS CUI [2,1])
C0683954 (UMLS CUI [2,2])
Tillbaka till toppen 

Kontakt

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Hjälp

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