ID

44743

Beschrijving

Evaluation of Radiation Induced Pulmonary Hypertension Using MRI in Stage III NSCLC Patients Treated With Chemoradiotherapy. A Pilot Study; ODM derived from: https://clinicaltrials.gov/show/NCT02377934

Link

https://clinicaltrials.gov/show/NCT02377934

Trefwoorden

Versies (1)
  1. 10-11-21 10-11-21 -
Houder van rechten

University Medical Center Groningen

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10 november 2021

DOI

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Creative Commons BY-NC 4.0
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Eligibility Pulmonary Hypertension NCT02377934

Engels

Eligibility Pulmonary Hypertension NCT02377934

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
age ≥ 18 years
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
who ps 0-2
Beschrijving

who ps

Datatype

boolean

Alias
UMLS CUI [1]
C1298650
histological or cytological confirmation of non-small cell lung cancer or an 18f-fdg-positive, growing mass on ct-thorax suggestive of nsclc.
Beschrijving

histological or cytological confirmation of non-small cell lung cancer or an 18f-fdg-positive, growing mass on ct-thorax suggestive of nsclc

Datatype

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C0750484
UMLS CUI [1,3]
C0019638
UMLS CUI [2,1]
C0007131
UMLS CUI [2,2]
C0750484
UMLS CUI [2,3]
C0010819
UMLS CUI [3,1]
C0007131
UMLS CUI [3,2]
C0040405
UMLS CUI [3,3]
C3641247
UMLS CUI [3,4]
C1514241
stage iiia or iiib
Beschrijving

tnm stage

Datatype

boolean

Alias
UMLS CUI [1,1]
C1515169
UMLS CUI [1,2]
C0475455
patients with extensive mediastinal lymph node involvement (such as n3), or large primary tumour size
Beschrijving

mediastinal lymph node involvement or large primary tumour size

Datatype

boolean

Alias
UMLS CUI [1,1]
C1515169
UMLS CUI [1,2]
C0456532
UMLS CUI [2,1]
C1515169
UMLS CUI [2,2]
C0475455
adequate pulmonary function estimated by flow volume curves
Beschrijving

adequate pulmonary function estimated by flow volume curves

Datatype

boolean

Alias
UMLS CUI [1,1]
C0231921
UMLS CUI [1,2]
C0205411
UMLS CUI [1,3]
C0024119
life expectancy of at least 6 months
Beschrijving

life expectancy

Datatype

boolean

Alias
UMLS CUI [1,1]
C0023671
UMLS CUI [1,2]
C0449238
UMLS CUI [1,3]
C1524031
absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol; those conditions should be discussed with the patient before registration in the trial.
Beschrijving

absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol

Datatype

boolean

Alias
UMLS CUI [1,1]
C0205486
UMLS CUI [1,2]
C0348080
UMLS CUI [1,3]
C0332197
UMLS CUI [1,4]
C1292733
UMLS CUI [1,5]
C0525058
UMLS CUI [2,1]
C0241888
UMLS CUI [2,2]
C0348080
UMLS CUI [2,3]
C0332197
UMLS CUI [2,4]
C1292733
UMLS CUI [2,5]
C0525058
UMLS CUI [3,1]
C3850138
UMLS CUI [3,2]
C0348080
UMLS CUI [3,3]
C0332197
UMLS CUI [3,4]
C1292733
UMLS CUI [3,5]
C0525058
UMLS CUI [4,1]
C0017444
UMLS CUI [4,2]
C0348080
UMLS CUI [4,3]
C0332197
UMLS CUI [4,4]
C1292733
UMLS CUI [4,5]
C0525058
planned for 25 x 2.4 gy, with concomitant chemotherapy
Beschrijving

planned radiotherapy with concomitant chemotherapy

Datatype

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C1301732
UMLS CUI [1,3]
C0392920
UMLS CUI [1,4]
C1707479
before patient registration, written informed consent will be obtained.
Beschrijving

written informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
presence of contra-indications for undergoing mri
Beschrijving

mri contra-indications

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
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Similar models

Eligibility Pulmonary Hypertension NCT02377934

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
age ≥ 18 years
boolean
C0001779 (UMLS CUI [1])
who ps
Item
who ps 0-2
boolean
C1298650 (UMLS CUI [1])
histological or cytological confirmation of non-small cell lung cancer or an 18f-fdg-positive, growing mass on ct-thorax suggestive of nsclc
Item
histological or cytological confirmation of non-small cell lung cancer or an 18f-fdg-positive, growing mass on ct-thorax suggestive of nsclc.
boolean
C0007131 (UMLS CUI [1,1])
C0750484 (UMLS CUI [1,2])
C0019638 (UMLS CUI [1,3])
C0007131 (UMLS CUI [2,1])
C0750484 (UMLS CUI [2,2])
C0010819 (UMLS CUI [2,3])
C0007131 (UMLS CUI [3,1])
C0040405 (UMLS CUI [3,2])
C3641247 (UMLS CUI [3,3])
C1514241 (UMLS CUI [3,4])
tnm stage
Item
stage iiia or iiib
boolean
C1515169 (UMLS CUI [1,1])
C0475455 (UMLS CUI [1,2])
mediastinal lymph node involvement or large primary tumour size
Item
patients with extensive mediastinal lymph node involvement (such as n3), or large primary tumour size
boolean
C1515169 (UMLS CUI [1,1])
C0456532 (UMLS CUI [1,2])
C1515169 (UMLS CUI [2,1])
C0475455 (UMLS CUI [2,2])
adequate pulmonary function estimated by flow volume curves
Item
adequate pulmonary function estimated by flow volume curves
boolean
C0231921 (UMLS CUI [1,1])
C0205411 (UMLS CUI [1,2])
C0024119 (UMLS CUI [1,3])
life expectancy
Item
life expectancy of at least 6 months
boolean
C0023671 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C1524031 (UMLS CUI [1,3])
absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol
Item
absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol; those conditions should be discussed with the patient before registration in the trial.
boolean
C0205486 (UMLS CUI [1,1])
C0348080 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C1292733 (UMLS CUI [1,4])
C0525058 (UMLS CUI [1,5])
C0241888 (UMLS CUI [2,1])
C0348080 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C1292733 (UMLS CUI [2,4])
C0525058 (UMLS CUI [2,5])
C3850138 (UMLS CUI [3,1])
C0348080 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
C1292733 (UMLS CUI [3,4])
C0525058 (UMLS CUI [3,5])
C0017444 (UMLS CUI [4,1])
C0348080 (UMLS CUI [4,2])
C0332197 (UMLS CUI [4,3])
C1292733 (UMLS CUI [4,4])
C0525058 (UMLS CUI [4,5])
planned radiotherapy with concomitant chemotherapy
Item
planned for 25 x 2.4 gy, with concomitant chemotherapy
boolean
C1522449 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
C1707479 (UMLS CUI [1,4])
written informed consent
Item
before patient registration, written informed consent will be obtained.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
mri contra-indications
Item
presence of contra-indications for undergoing mri
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
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