ID

31729

Descrizione

Bosentan in Pulmonary Hypertension in Interstitial Lung Disease Treatment Study; ODM derived from: https://clinicaltrials.gov/show/NCT00637065

collegamento

https://clinicaltrials.gov/show/NCT00637065

Keywords

versioni (2)
  1. 23/09/18 23/09/18 -
  2. 23/09/18 23/09/18 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

23 settembre 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0
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Eligibility Pulmonary Hypertension NCT00637065

Inglese

Eligibility Pulmonary Hypertension NCT00637065

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. patients >=18yrs, <80yrs
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
2. patients with idiopathic pulmonary fibrosis (ipf) or idiopathic fibrotic non-specific interstitial pneumonitis (nsip) confirmed by their respiratory physician according to ats/ers criteria.
Descrizione

Idiopathic Pulmonary Fibrosis | Idiopathic nonspecific interstitial pneumonitis fibrotic

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1800706
UMLS CUI [2,1]
C3250406
UMLS CUI [2,2]
C0334129
3. patients with pulmonary hypertension on right heart catheter (mean pulmonary arterial pressure >=25mmhg with pulmonary artery occlusion pressure, left atrial pressure or left ventricular end-diastolic pressure <15mmhg).
Descrizione

Pulmonary Hypertension Catheterization of right heart | Mean pulmonary arterial pressure | Pulmonary Artery Occlusion Pressure | Left atrial pressure | Left ventricular end-diastolic pressure measurement

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0020542
UMLS CUI [1,2]
C0189896
UMLS CUI [2]
C3854605
UMLS CUI [3]
C0034094
UMLS CUI [4]
C0456170
UMLS CUI [5]
C1171395
4. patients providing written informed consent.
Descrizione

Informed Consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. patients <18, >80yrs.
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
2. patients with unstable disease, or an acute exacerbation of their underlying fibrotic lung disease.
Descrizione

Disease Unstable | Pulmonary Fibrosis Exacerbation

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0443343
UMLS CUI [2,1]
C0034069
UMLS CUI [2,2]
C4086268
3. patients with significant other organ co-morbidity including hepatic or renal impairment.
Descrizione

Organ Comorbidity | Hepatic impairment | Renal Insufficiency

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0178784
UMLS CUI [1,2]
C0009488
UMLS CUI [2]
C0948807
UMLS CUI [3]
C1565489
4. patients with systolic bp < 85mmhg
Descrizione

Systolic Pressure

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0871470
5. patients with other conditions that may affect the ability to perform a 6-minute walk test.
Descrizione

Condition Affecting 6-Minute Walk Test

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0430515
6. patients unable to provide informed consent and comply with the patient protocol.
Descrizione

Informed Consent Unable | Protocol Compliance Unable

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0525058
UMLS CUI [2,2]
C1299582
7. patients receiving excluded medications (including: epoprostenol, or prostacyclin analogues, phosphodiesterase inhibitors, other endothelin receptor antagonists, drugs with potential interaction with bosentan such as glibenclamide, fluconazole, cyclosporin a, or tacrolimus, and other investigational agents).
Descrizione

Pharmaceutical Preparations Excluded | Epoprostenol | Prostaglandin Analog | Phosphodiesterase Inhibitors | Endothelin receptor antagonist | Pharmaceutical Preparations Interaction Bosentan | Glyburide | Fluconazole | Cyclosporine | Tacrolimus | Investigational New Drugs

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0332196
UMLS CUI [2]
C0033567
UMLS CUI [3]
C3536889
UMLS CUI [4]
C0031638
UMLS CUI [5]
C1134681
UMLS CUI [6,1]
C0013227
UMLS CUI [6,2]
C1704675
UMLS CUI [6,3]
C0252643
UMLS CUI [7]
C0017628
UMLS CUI [8]
C0016277
UMLS CUI [9]
C0010592
UMLS CUI [10]
C0085149
UMLS CUI [11]
C0013230
8. patients with planned surgical intervention during the study period.
Descrizione

Surgical intervention Planned

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0549433
UMLS CUI [1,2]
C1301732
9. pregnant patients or women of child-bearing age, who are not using a reliable contraceptive method.
Descrizione

Pregnancy | Childbearing Potential Contraceptive methods Absent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2,1]
C3831118
UMLS CUI [2,2]
C0700589
UMLS CUI [2,3]
C0332197
10. patients with clinically overt ischaemic heart disease.
Descrizione

Myocardial Ischemia

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0151744
11. patients with predominant emphysema on high resolution ct scan (emphysema greater in extent than interstitial changes).
Descrizione

Emphysema Predominant High resolution CT

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0034067
UMLS CUI [1,2]
C1542147
UMLS CUI [1,3]
C1512457
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Similar models

Eligibility Pulmonary Hypertension NCT00637065

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
1. patients >=18yrs, <80yrs
boolean
C0001779 (UMLS CUI [1])
Idiopathic Pulmonary Fibrosis | Idiopathic nonspecific interstitial pneumonitis fibrotic
Item
2. patients with idiopathic pulmonary fibrosis (ipf) or idiopathic fibrotic non-specific interstitial pneumonitis (nsip) confirmed by their respiratory physician according to ats/ers criteria.
boolean
C1800706 (UMLS CUI [1])
C3250406 (UMLS CUI [2,1])
C0334129 (UMLS CUI [2,2])
Pulmonary Hypertension Catheterization of right heart | Mean pulmonary arterial pressure | Pulmonary Artery Occlusion Pressure | Left atrial pressure | Left ventricular end-diastolic pressure measurement
Item
3. patients with pulmonary hypertension on right heart catheter (mean pulmonary arterial pressure >=25mmhg with pulmonary artery occlusion pressure, left atrial pressure or left ventricular end-diastolic pressure <15mmhg).
boolean
C0020542 (UMLS CUI [1,1])
C0189896 (UMLS CUI [1,2])
C3854605 (UMLS CUI [2])
C0034094 (UMLS CUI [3])
C0456170 (UMLS CUI [4])
C1171395 (UMLS CUI [5])
Informed Consent
Item
4. patients providing written informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Age
Item
1. patients <18, >80yrs.
boolean
C0001779 (UMLS CUI [1])
Disease Unstable | Pulmonary Fibrosis Exacerbation
Item
2. patients with unstable disease, or an acute exacerbation of their underlying fibrotic lung disease.
boolean
C0012634 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C0034069 (UMLS CUI [2,1])
C4086268 (UMLS CUI [2,2])
Organ Comorbidity | Hepatic impairment | Renal Insufficiency
Item
3. patients with significant other organ co-morbidity including hepatic or renal impairment.
boolean
C0178784 (UMLS CUI [1,1])
C0009488 (UMLS CUI [1,2])
C0948807 (UMLS CUI [2])
C1565489 (UMLS CUI [3])
Systolic Pressure
Item
4. patients with systolic bp < 85mmhg
boolean
C0871470 (UMLS CUI [1])
Condition Affecting 6-Minute Walk Test
Item
5. patients with other conditions that may affect the ability to perform a 6-minute walk test.
boolean
C0348080 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0430515 (UMLS CUI [1,3])
Informed Consent Unable | Protocol Compliance Unable
Item
6. patients unable to provide informed consent and comply with the patient protocol.
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Pharmaceutical Preparations Excluded | Epoprostenol | Prostaglandin Analog | Phosphodiesterase Inhibitors | Endothelin receptor antagonist | Pharmaceutical Preparations Interaction Bosentan | Glyburide | Fluconazole | Cyclosporine | Tacrolimus | Investigational New Drugs
Item
7. patients receiving excluded medications (including: epoprostenol, or prostacyclin analogues, phosphodiesterase inhibitors, other endothelin receptor antagonists, drugs with potential interaction with bosentan such as glibenclamide, fluconazole, cyclosporin a, or tacrolimus, and other investigational agents).
boolean
C0013227 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0033567 (UMLS CUI [2])
C3536889 (UMLS CUI [3])
C0031638 (UMLS CUI [4])
C1134681 (UMLS CUI [5])
C0013227 (UMLS CUI [6,1])
C1704675 (UMLS CUI [6,2])
C0252643 (UMLS CUI [6,3])
C0017628 (UMLS CUI [7])
C0016277 (UMLS CUI [8])
C0010592 (UMLS CUI [9])
C0085149 (UMLS CUI [10])
C0013230 (UMLS CUI [11])
Surgical intervention Planned
Item
8. patients with planned surgical intervention during the study period.
boolean
C0549433 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
Pregnancy | Childbearing Potential Contraceptive methods Absent
Item
9. pregnant patients or women of child-bearing age, who are not using a reliable contraceptive method.
boolean
C0032961 (UMLS CUI [1])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
Myocardial Ischemia
Item
10. patients with clinically overt ischaemic heart disease.
boolean
C0151744 (UMLS CUI [1])
Emphysema Predominant High resolution CT
Item
11. patients with predominant emphysema on high resolution ct scan (emphysema greater in extent than interstitial changes).
boolean
C0034067 (UMLS CUI [1,1])
C1542147 (UMLS CUI [1,2])
C1512457 (UMLS CUI [1,3])
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