ID

39985

Description

Sympathetic Activity and Renal Denervation; ODM derived from: https://clinicaltrials.gov/show/NCT01355055

Lien

https://clinicaltrials.gov/show/NCT01355055

Mots-clés

Versions (1)
  1. 08/03/2020 08/03/2020 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

8 mars 2020

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Retour au modèle Commentaires
Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Hypertension NCT01355055

Anglais

Eligibility Hypertension NCT01355055

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
refractory hypertension (as defined by the who: poorly controlled hypertension (>140/90 mmhg) despite adequate doses of at least three antihypertensive drugs including a diuretic)
Description

Refractory hypertension | Poor hypertension control | Blood pressure determination | Antihypertensive Agents Quantity Dose | Diuretics

Type de données

boolean

Alias
UMLS CUI [1]
C0860493
UMLS CUI [2]
C0421190
UMLS CUI [3]
C0005824
UMLS CUI [4,1]
C0003364
UMLS CUI [4,2]
C1265611
UMLS CUI [4,3]
C0178602
UMLS CUI [5]
C0012798
men or women aged >18 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
intact peroneal nerve
Description

Peroneal Nerve Intact

Type de données

boolean

Alias
UMLS CUI [1,1]
C4316912
UMLS CUI [1,2]
C0205266
written informed consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
diseases, dysfunctions, or medications (such as net inhibitors) that exclude a participation in the study according to the investigator.
Description

Disease Study Subject Participation Status Excluded | Dysfunction Study Subject Participation Status Excluded | Pharmaceutical Preparations Study Subject Participation Status Excluded | Norepinephrine Transporter Inhibitors

Type de données

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C0332196
UMLS CUI [2,1]
C3887504
UMLS CUI [2,2]
C2348568
UMLS CUI [2,3]
C0332196
UMLS CUI [3,1]
C0013227
UMLS CUI [3,2]
C2348568
UMLS CUI [3,3]
C0332196
UMLS CUI [4,1]
C0132800
UMLS CUI [4,2]
C0243077
legal incompetence or circumstances that interfere with the patient´s ability to fully understand scope, relevance, and/or consequences of participation in this study.
Description

Incompetence Legal | Life circumstance problem Interferes with Comprehension Study Protocol

Type de données

boolean

Alias
UMLS CUI [1,1]
C0231189
UMLS CUI [1,2]
C1301860
UMLS CUI [2,1]
C0868647
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0162340
UMLS CUI [2,4]
C2348563
people in custody
Description

People Guardianship

Type de données

boolean

Alias
UMLS CUI [1,1]
C0027361
UMLS CUI [1,2]
C0870627
hypersensitivity to clonidine, phenylephrine, or nitroprusside-sodium
Description

Clonidine allergy | Phenylephrine allergy | Sodium nitroprusside allergy

Type de données

boolean

Alias
UMLS CUI [1]
C0570975
UMLS CUI [2]
C0570949
UMLS CUI [3]
C0571973
sick sinus syndrome, second or third degree av block, bradycardia < 50 bpm (contraindication for clonidine)
Description

Sick Sinus Syndrome | Second degree atrioventricular block | Complete atrioventricular block | Bradycardia | Medical contraindication Clonidine

Type de données

boolean

Alias
UMLS CUI [1]
C0037052
UMLS CUI [2]
C0264906
UMLS CUI [3]
C0151517
UMLS CUI [4]
C0428977
UMLS CUI [5,1]
C1301624
UMLS CUI [5,2]
C0009014
endogenous depression (contraindication for clonidine)
Description

Endogenous depression | Medical contraindication Clonidine

Type de données

boolean

Alias
UMLS CUI [1]
C0011573
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0009014
Retour au début de la page

Similar models

Eligibility Hypertension NCT01355055

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Refractory hypertension | Poor hypertension control | Blood pressure determination | Antihypertensive Agents Quantity Dose | Diuretics
Item
refractory hypertension (as defined by the who: poorly controlled hypertension (>140/90 mmhg) despite adequate doses of at least three antihypertensive drugs including a diuretic)
boolean
C0860493 (UMLS CUI [1])
C0421190 (UMLS CUI [2])
C0005824 (UMLS CUI [3])
C0003364 (UMLS CUI [4,1])
C1265611 (UMLS CUI [4,2])
C0178602 (UMLS CUI [4,3])
C0012798 (UMLS CUI [5])
Age
Item
men or women aged >18 years
boolean
C0001779 (UMLS CUI [1])
Peroneal Nerve Intact
Item
intact peroneal nerve
boolean
C4316912 (UMLS CUI [1,1])
C0205266 (UMLS CUI [1,2])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Disease Study Subject Participation Status Excluded | Dysfunction Study Subject Participation Status Excluded | Pharmaceutical Preparations Study Subject Participation Status Excluded | Norepinephrine Transporter Inhibitors
Item
diseases, dysfunctions, or medications (such as net inhibitors) that exclude a participation in the study according to the investigator.
boolean
C0012634 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C0332196 (UMLS CUI [1,3])
C3887504 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C0332196 (UMLS CUI [2,3])
C0013227 (UMLS CUI [3,1])
C2348568 (UMLS CUI [3,2])
C0332196 (UMLS CUI [3,3])
C0132800 (UMLS CUI [4,1])
C0243077 (UMLS CUI [4,2])
Incompetence Legal | Life circumstance problem Interferes with Comprehension Study Protocol
Item
legal incompetence or circumstances that interfere with the patient´s ability to fully understand scope, relevance, and/or consequences of participation in this study.
boolean
C0231189 (UMLS CUI [1,1])
C1301860 (UMLS CUI [1,2])
C0868647 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0162340 (UMLS CUI [2,3])
C2348563 (UMLS CUI [2,4])
People Guardianship
Item
people in custody
boolean
C0027361 (UMLS CUI [1,1])
C0870627 (UMLS CUI [1,2])
Clonidine allergy | Phenylephrine allergy | Sodium nitroprusside allergy
Item
hypersensitivity to clonidine, phenylephrine, or nitroprusside-sodium
boolean
C0570975 (UMLS CUI [1])
C0570949 (UMLS CUI [2])
C0571973 (UMLS CUI [3])
Sick Sinus Syndrome | Second degree atrioventricular block | Complete atrioventricular block | Bradycardia | Medical contraindication Clonidine
Item
sick sinus syndrome, second or third degree av block, bradycardia < 50 bpm (contraindication for clonidine)
boolean
C0037052 (UMLS CUI [1])
C0264906 (UMLS CUI [2])
C0151517 (UMLS CUI [3])
C0428977 (UMLS CUI [4])
C1301624 (UMLS CUI [5,1])
C0009014 (UMLS CUI [5,2])
Endogenous depression | Medical contraindication Clonidine
Item
endogenous depression (contraindication for clonidine)
boolean
C0011573 (UMLS CUI [1])
C1301624 (UMLS CUI [2,1])
C0009014 (UMLS CUI [2,2])
Retour au début de la page 

Contact

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Aide

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