ID

22861

Description

Dose Determination Safety and Activity Study of Inhaled NX1011 to Treat Pulmonary Arterial Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00323024

Lien

https://clinicaltrials.gov/show/NCT00323024

Mots-clés

Versions (1)
  1. 13/06/2017 13/06/2017 -
Téléchargé le

13 juin 2017

DOI

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Licence

Creative Commons BY 4.0
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Eligibility Pulmonary Hypertension NCT00323024

Anglais

Eligibility Pulmonary Hypertension NCT00323024

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient must either:
Description

Criteria Fulfill

Type de données

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
meet the pah diagnostic criteria at screening (based on a documented history of diagnosis as outlined in the american college of chest physicians [accp] 2004 evidence-based clinical practices guidelines)15; or
Description

Pulmonary arterial hypertension

Type de données

boolean

Alias
UMLS CUI [1]
C2973725
have elevated pulmonary pressure with a suspected pah diagnosis based on a clinical referral at screening for a rhc.
Description

Pulmonary arterial pressure elevated | Pulmonary arterial hypertension Suspected | Clinical referral Catheterization of right heart

Type de données

boolean

Alias
UMLS CUI [1]
C3670875
UMLS CUI [2,1]
C2973725
UMLS CUI [2,2]
C0332147
UMLS CUI [3,1]
C1545725
UMLS CUI [3,2]
C0189896
patient must have pah as defined by a mean pulmonary artery pressure (pap) > 25 mmhg.
Description

Pulmonary arterial hypertension | Pulmonary artery mean pressure

Type de données

boolean

Alias
UMLS CUI [1]
C2973725
UMLS CUI [2]
C0428645
patient must have symptoms of pulmonary hypertension (ph) according to the world health organization (who) functional classification of pulmonary hypertension class ii through iv.
Description

Symptoms Pulmonary Hypertension | WHO Pulmonary arterial hypertension Class Functional

Type de données

boolean

Alias
UMLS CUI [1,1]
C1457887
UMLS CUI [1,2]
C0020542
UMLS CUI [2,1]
C0043237
UMLS CUI [2,2]
C2973725
UMLS CUI [2,3]
C0456387
UMLS CUI [2,4]
C0205245
patient must consent to, be able to tolerate, and have adequate venous and arterial access for swan-ganz catheterization (sgc) and an arterial line.
Description

Venous access Swan-Ganz Catheterization | Access Arterial Swan-Ganz Catheterization | Arterial Line

Type de données

boolean

Alias
UMLS CUI [1,1]
C3164222
UMLS CUI [1,2]
C0007438
UMLS CUI [2,1]
C0444454
UMLS CUI [2,2]
C0221464
UMLS CUI [2,3]
C0007438
UMLS CUI [3]
C0003835
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
clinically significant right-to-left intracardiac shunts based on doppler echocardiography with bubble study.
Description

Shunt right-left intracardiac Doppler Echocardiography

Type de données

boolean

Alias
UMLS CUI [1,1]
C0489644
UMLS CUI [1,2]
C0013520
history of pulmonary veno-occlusive disease or clinically significant aortic or mitral stenosis.
Description

Pulmonary Veno-Occlusive Disease | Aortic Valve Stenosis | Mitral Valve Stenosis

Type de données

boolean

Alias
UMLS CUI [1]
C0034091
UMLS CUI [2]
C0003507
UMLS CUI [3]
C0026269
history of sustained ventricular tachycardia (vt-s) or ventricular fibrillation (vf) and cardiac arrest, or presence of atrial fibrillation.
Description

Sustained ventricular tachycardia | Ventricular Fibrillation | Cardiac Arrest | Atrial Fibrillation

Type de données

boolean

Alias
UMLS CUI [1]
C0750197
UMLS CUI [2]
C0042510
UMLS CUI [3]
C0018790
UMLS CUI [4]
C0004238
active cardiac disease meeting the following criteria:
Description

Heart Disease

Type de données

boolean

Alias
UMLS CUI [1]
C0018799
patient with elevated pulmonary capillary wedge pressures (pcwps) > 25 mmhg.
Description

Increased pulmonary arterial wedge pressure

Type de données

boolean

Alias
UMLS CUI [1]
C0520850
patient with a history of myocardial infarction or coronary intervention within the last 60 days.
Description

Myocardial Infarction | Percutaneous Coronary Intervention

Type de données

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C1532338
patient with a history of pacemaker, cardiac defibrillator, or biventricular pacemaker insertion within 4 weeks of baseline.
Description

Artificial cardiac pacemaker | Cardiac defibrillator | Biventricular pacemaker insertion

Type de données

boolean

Alias
UMLS CUI [1]
C0030163
UMLS CUI [2]
C1391956
UMLS CUI [3]
C3805138
patient who cannot be withdrawn from nitrate therapy.
Description

Nitrates therapy Withdrawal Unsuccessful

Type de données

boolean

Alias
UMLS CUI [1,1]
C0028125
UMLS CUI [1,2]
C0039798
UMLS CUI [1,3]
C2349954
UMLS CUI [1,4]
C1272705
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Similar models

Eligibility Pulmonary Hypertension NCT00323024

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Criteria Fulfill
Item
patient must either:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Pulmonary arterial hypertension
Item
meet the pah diagnostic criteria at screening (based on a documented history of diagnosis as outlined in the american college of chest physicians [accp] 2004 evidence-based clinical practices guidelines)15; or
boolean
C2973725 (UMLS CUI [1])
Pulmonary arterial pressure elevated | Pulmonary arterial hypertension Suspected | Clinical referral Catheterization of right heart
Item
have elevated pulmonary pressure with a suspected pah diagnosis based on a clinical referral at screening for a rhc.
boolean
C3670875 (UMLS CUI [1])
C2973725 (UMLS CUI [2,1])
C0332147 (UMLS CUI [2,2])
C1545725 (UMLS CUI [3,1])
C0189896 (UMLS CUI [3,2])
Pulmonary arterial hypertension | Pulmonary artery mean pressure
Item
patient must have pah as defined by a mean pulmonary artery pressure (pap) > 25 mmhg.
boolean
C2973725 (UMLS CUI [1])
C0428645 (UMLS CUI [2])
Symptoms Pulmonary Hypertension | WHO Pulmonary arterial hypertension Class Functional
Item
patient must have symptoms of pulmonary hypertension (ph) according to the world health organization (who) functional classification of pulmonary hypertension class ii through iv.
boolean
C1457887 (UMLS CUI [1,1])
C0020542 (UMLS CUI [1,2])
C0043237 (UMLS CUI [2,1])
C2973725 (UMLS CUI [2,2])
C0456387 (UMLS CUI [2,3])
C0205245 (UMLS CUI [2,4])
Venous access Swan-Ganz Catheterization | Access Arterial Swan-Ganz Catheterization | Arterial Line
Item
patient must consent to, be able to tolerate, and have adequate venous and arterial access for swan-ganz catheterization (sgc) and an arterial line.
boolean
C3164222 (UMLS CUI [1,1])
C0007438 (UMLS CUI [1,2])
C0444454 (UMLS CUI [2,1])
C0221464 (UMLS CUI [2,2])
C0007438 (UMLS CUI [2,3])
C0003835 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Shunt right-left intracardiac Doppler Echocardiography
Item
clinically significant right-to-left intracardiac shunts based on doppler echocardiography with bubble study.
boolean
C0489644 (UMLS CUI [1,1])
C0013520 (UMLS CUI [1,2])
Pulmonary Veno-Occlusive Disease | Aortic Valve Stenosis | Mitral Valve Stenosis
Item
history of pulmonary veno-occlusive disease or clinically significant aortic or mitral stenosis.
boolean
C0034091 (UMLS CUI [1])
C0003507 (UMLS CUI [2])
C0026269 (UMLS CUI [3])
Sustained ventricular tachycardia | Ventricular Fibrillation | Cardiac Arrest | Atrial Fibrillation
Item
history of sustained ventricular tachycardia (vt-s) or ventricular fibrillation (vf) and cardiac arrest, or presence of atrial fibrillation.
boolean
C0750197 (UMLS CUI [1])
C0042510 (UMLS CUI [2])
C0018790 (UMLS CUI [3])
C0004238 (UMLS CUI [4])
Heart Disease
Item
active cardiac disease meeting the following criteria:
boolean
C0018799 (UMLS CUI [1])
Increased pulmonary arterial wedge pressure
Item
patient with elevated pulmonary capillary wedge pressures (pcwps) > 25 mmhg.
boolean
C0520850 (UMLS CUI [1])
Myocardial Infarction | Percutaneous Coronary Intervention
Item
patient with a history of myocardial infarction or coronary intervention within the last 60 days.
boolean
C0027051 (UMLS CUI [1])
C1532338 (UMLS CUI [2])
Artificial cardiac pacemaker | Cardiac defibrillator | Biventricular pacemaker insertion
Item
patient with a history of pacemaker, cardiac defibrillator, or biventricular pacemaker insertion within 4 weeks of baseline.
boolean
C0030163 (UMLS CUI [1])
C1391956 (UMLS CUI [2])
C3805138 (UMLS CUI [3])
Nitrates therapy Withdrawal Unsuccessful
Item
patient who cannot be withdrawn from nitrate therapy.
boolean
C0028125 (UMLS CUI [1,1])
C0039798 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,3])
C1272705 (UMLS CUI [1,4])
Retour au début de la page 

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