ID

39962

Descrizione

Telmisartan 80mg Non-responder Trial; ODM derived from: https://clinicaltrials.gov/show/NCT01222520

collegamento

https://clinicaltrials.gov/show/NCT01222520

Keywords

versioni (1)
  1. 06/03/20 06/03/20 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

6 marzo 2020

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
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Eligibility Hypertension NCT01222520

Inglese

Eligibility Hypertension NCT01222520

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
essential hypertensive patients
Descrizione

Essential Hypertension

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0085580
if already taking antihypertensive drugs, mean seated diastolic blood pressure (dbp) must be >=90 and >=114 mmhg
Descrizione

Antihypertensive Agents | Sitting diastolic blood pressure mean

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0003364
UMLS CUI [2,1]
C1319894
UMLS CUI [2,2]
C0444504
if not taking any antihypertensive drugs, mean seated dbp must be >=95 and >=114 mmhg
Descrizione

Antihypertensive Agents Absent | Sitting diastolic blood pressure mean

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C1319894
UMLS CUI [2,2]
C0444504
able to stop all current antihypertensive drugs without risk to the patient based on the investigators opinion.
Descrizione

Ability Discontinue Antihypertensive Agents | Risk Absent Patient

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0085732
UMLS CUI [1,2]
C1444662
UMLS CUI [1,3]
C0003364
UMLS CUI [2,1]
C0035647
UMLS CUI [2,2]
C0332197
UMLS CUI [2,3]
C0030705
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients taking 3 or more antihypertensive drugs at signing the informed consent form
Descrizione

Antihypertensive Agents Quantity

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C1265611
patients with known or suspected secondary hypertension
Descrizione

Secondary hypertension | Secondary hypertension Suspected

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0155616
UMLS CUI [2,1]
C0155616
UMLS CUI [2,2]
C0750491
patients with clinically relevant cardiac arrhythmia
Descrizione

Cardiac Arrhythmia

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0003811
congestive heart failure with new york heart association (nyha) functional class iii-iv
Descrizione

Congestive heart failure New York Heart Association Classification

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C1275491
patients with recent cardiovascular events
Descrizione

Cardiovascular event Recent

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1320716
UMLS CUI [1,2]
C0332185
patients with a history of stroke or transient ischaemic attack within last 6 months before signing the informed consent form
Descrizione

Cerebrovascular accident | Transient Ischemic Attack

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0038454
UMLS CUI [2]
C0007787
patients with a history of sudden deterioration of renal function with angiotensin ii receptor blockers (arbs) or angiotensin converting enzyme (ace) inhibitors; or patients with post-renal transplant or post-nephrectomy
Descrizione

Deterioration Sudden Renal function | Angiotensin II receptor antagonist | Angiotensin-Converting Enzyme Inhibitors | Status post Kidney Transplantation | Status post Nephrectomy

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0868945
UMLS CUI [1,2]
C1276802
UMLS CUI [1,3]
C0232804
UMLS CUI [2]
C0521942
UMLS CUI [3]
C0003015
UMLS CUI [4,1]
C0231290
UMLS CUI [4,2]
C0022671
UMLS CUI [5,1]
C0231290
UMLS CUI [5,2]
C0027695
patients who have previously experienced characteristic symptoms of angioedema (such as facial, tongue, pharyngeal, or laryngeal swelling with dyspnea) during treatment with arbs or ace inhibitors
Descrizione

Symptoms Angioedema | Facial swelling with Dyspnea | Tongue swelling with Dyspnea | Pharyngeal swelling with Dyspnea | Laryngeal Edema with Dyspnea

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1457887
UMLS CUI [1,2]
C0002994
UMLS CUI [2,1]
C0151602
UMLS CUI [2,2]
C0332287
UMLS CUI [2,3]
C0013404
UMLS CUI [3,1]
C0236068
UMLS CUI [3,2]
C0332287
UMLS CUI [3,3]
C0013404
UMLS CUI [4,1]
C1704205
UMLS CUI [4,2]
C0332287
UMLS CUI [4,3]
C0013404
UMLS CUI [5,1]
C0023052
UMLS CUI [5,2]
C0332287
UMLS CUI [5,3]
C0013404
patients with known hypersensitivity to any component of the investigational product, or a known hypersensitivity to dihydropyridine-derived drugs
Descrizione

Hypersensitivity Investigational New Drug Component | Hypersensitivity Dihydropyridine derivatives

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230
UMLS CUI [1,3]
C1705248
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C3653438
patients with hepatic and/or renal dysfunction
Descrizione

Liver Dysfunction | Renal dysfunction

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0086565
UMLS CUI [2]
C3279454
pre-menopausal women who are nursing or pregnant
Descrizione

Premenopausal state | Breast Feeding | Pregnancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0232969
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032961
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Similar models

Eligibility Hypertension NCT01222520

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Essential Hypertension
Item
essential hypertensive patients
boolean
C0085580 (UMLS CUI [1])
Antihypertensive Agents | Sitting diastolic blood pressure mean
Item
if already taking antihypertensive drugs, mean seated diastolic blood pressure (dbp) must be >=90 and >=114 mmhg
boolean
C0003364 (UMLS CUI [1])
C1319894 (UMLS CUI [2,1])
C0444504 (UMLS CUI [2,2])
Antihypertensive Agents Absent | Sitting diastolic blood pressure mean
Item
if not taking any antihypertensive drugs, mean seated dbp must be >=95 and >=114 mmhg
boolean
C0003364 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C1319894 (UMLS CUI [2,1])
C0444504 (UMLS CUI [2,2])
Ability Discontinue Antihypertensive Agents | Risk Absent Patient
Item
able to stop all current antihypertensive drugs without risk to the patient based on the investigators opinion.
boolean
C0085732 (UMLS CUI [1,1])
C1444662 (UMLS CUI [1,2])
C0003364 (UMLS CUI [1,3])
C0035647 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0030705 (UMLS CUI [2,3])
Item Group
C0680251 (UMLS CUI)
Antihypertensive Agents Quantity
Item
patients taking 3 or more antihypertensive drugs at signing the informed consent form
boolean
C0003364 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Secondary hypertension | Secondary hypertension Suspected
Item
patients with known or suspected secondary hypertension
boolean
C0155616 (UMLS CUI [1])
C0155616 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
Cardiac Arrhythmia
Item
patients with clinically relevant cardiac arrhythmia
boolean
C0003811 (UMLS CUI [1])
Congestive heart failure New York Heart Association Classification
Item
congestive heart failure with new york heart association (nyha) functional class iii-iv
boolean
C0018802 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Cardiovascular event Recent
Item
patients with recent cardiovascular events
boolean
C1320716 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
Cerebrovascular accident | Transient Ischemic Attack
Item
patients with a history of stroke or transient ischaemic attack within last 6 months before signing the informed consent form
boolean
C0038454 (UMLS CUI [1])
C0007787 (UMLS CUI [2])
Deterioration Sudden Renal function | Angiotensin II receptor antagonist | Angiotensin-Converting Enzyme Inhibitors | Status post Kidney Transplantation | Status post Nephrectomy
Item
patients with a history of sudden deterioration of renal function with angiotensin ii receptor blockers (arbs) or angiotensin converting enzyme (ace) inhibitors; or patients with post-renal transplant or post-nephrectomy
boolean
C0868945 (UMLS CUI [1,1])
C1276802 (UMLS CUI [1,2])
C0232804 (UMLS CUI [1,3])
C0521942 (UMLS CUI [2])
C0003015 (UMLS CUI [3])
C0231290 (UMLS CUI [4,1])
C0022671 (UMLS CUI [4,2])
C0231290 (UMLS CUI [5,1])
C0027695 (UMLS CUI [5,2])
Symptoms Angioedema | Facial swelling with Dyspnea | Tongue swelling with Dyspnea | Pharyngeal swelling with Dyspnea | Laryngeal Edema with Dyspnea
Item
patients who have previously experienced characteristic symptoms of angioedema (such as facial, tongue, pharyngeal, or laryngeal swelling with dyspnea) during treatment with arbs or ace inhibitors
boolean
C1457887 (UMLS CUI [1,1])
C0002994 (UMLS CUI [1,2])
C0151602 (UMLS CUI [2,1])
C0332287 (UMLS CUI [2,2])
C0013404 (UMLS CUI [2,3])
C0236068 (UMLS CUI [3,1])
C0332287 (UMLS CUI [3,2])
C0013404 (UMLS CUI [3,3])
C1704205 (UMLS CUI [4,1])
C0332287 (UMLS CUI [4,2])
C0013404 (UMLS CUI [4,3])
C0023052 (UMLS CUI [5,1])
C0332287 (UMLS CUI [5,2])
C0013404 (UMLS CUI [5,3])
Hypersensitivity Investigational New Drug Component | Hypersensitivity Dihydropyridine derivatives
Item
patients with known hypersensitivity to any component of the investigational product, or a known hypersensitivity to dihydropyridine-derived drugs
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C1705248 (UMLS CUI [1,3])
C0020517 (UMLS CUI [2,1])
C3653438 (UMLS CUI [2,2])
Liver Dysfunction | Renal dysfunction
Item
patients with hepatic and/or renal dysfunction
boolean
C0086565 (UMLS CUI [1])
C3279454 (UMLS CUI [2])
Premenopausal state | Breast Feeding | Pregnancy
Item
pre-menopausal women who are nursing or pregnant
boolean
C0232969 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032961 (UMLS CUI [3])
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