ID

40340

Description

The Role of Gut Microbiota in Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT02188381

Lien

https://clinicaltrials.gov/show/NCT02188381

Mots-clés

Versions (1)
  1. 09/04/2020 09/04/2020 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

9 avril 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 NCT02188381

Anglais

Eligibility Hypertension NCT02188381

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age >18 and <80
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
is competent and willing to provide consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
inclusion criteria for each subject group:
Description

Study Subject Group Each

Type de données

boolean

Alias
UMLS CUI [1,1]
C0681850
UMLS CUI [1,2]
C0441833
UMLS CUI [1,3]
C1457900
control subjects will have a systolic bp <140mmhg with no cardiovascular disease
Description

Control Groups | Systolic Pressure | Cardiovascular Disease Absent

Type de données

boolean

Alias
UMLS CUI [1]
C0009932
UMLS CUI [2]
C0871470
UMLS CUI [3,1]
C0007222
UMLS CUI [3,2]
C0332197
patients with controlled hypertension
Description

Hypertensive disease Controlled

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C2911690
resistant hypertension subjects will have systolic blood pressure (bp) ≥140 mmhg despite ≥3 anti-hypertensive medications of different classes
Description

HYPERTENSION RESISTANT | Systolic Pressure | Antihypertensive Agents Quantity | Antihypertensive Agents Class Different

Type de données

boolean

Alias
UMLS CUI [1]
C0745130
UMLS CUI [2]
C0871470
UMLS CUI [3,1]
C0003364
UMLS CUI [3,2]
C1265611
UMLS CUI [4,1]
C0003364
UMLS CUI [4,2]
C0456387
UMLS CUI [4,3]
C1705242
subjects participating in nct 02133872 will be eligible to participate
Description

Study Subject Participation Status | Clinical Trial Specified

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0008976
UMLS CUI [2,2]
C0205369
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
currently pregnant or have been pregnant in the last 6 months;
Description

Pregnancy | Pregnancy Recent

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2,1]
C0032961
UMLS CUI [2,2]
C0332185
antibiotic treatment within 2 months of study enrollment;
Description

Antibiotic therapy Recent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0338237
UMLS CUI [1,2]
C0332185
currently taking a medication (e.g., antibiotic, anti-inflammatory agents, glucocorticoids or other immune modulating medications);
Description

Antibiotics | Anti-Inflammatory Agents | Glucocorticoids | Biological Response Modifiers

Type de données

boolean

Alias
UMLS CUI [1]
C0003232
UMLS CUI [2]
C0003209
UMLS CUI [3]
C0017710
UMLS CUI [4]
C0005525
unwilling to discontinue vitamin or supplements, including probiotics, potentially affecting gut microbiota (vitamins/supplements and medications that possibly affect the gut microbiota should be discontinued for at least 2wks prior to stool collection);
Description

Vitamins Discontinue Unwilling | Supplements Discontinue Unwilling | Probiotics Discontinue Unwilling | Vitamins Affecting Intestinal Microbiome | Supplements Affecting Intestinal Microbiome | Probiotics Affecting Intestinal Microbiome

Type de données

boolean

Alias
UMLS CUI [1,1]
C0042890
UMLS CUI [1,2]
C1444662
UMLS CUI [1,3]
C0558080
UMLS CUI [2,1]
C0242295
UMLS CUI [2,2]
C1444662
UMLS CUI [2,3]
C0558080
UMLS CUI [3,1]
C0525033
UMLS CUI [3,2]
C1444662
UMLS CUI [3,3]
C0558080
UMLS CUI [4,1]
C0042890
UMLS CUI [4,2]
C0392760
UMLS CUI [4,3]
C2985398
UMLS CUI [5,1]
C0242295
UMLS CUI [5,2]
C0392760
UMLS CUI [5,3]
C2985398
UMLS CUI [6,1]
C0525033
UMLS CUI [6,2]
C0392760
UMLS CUI [6,3]
C2985398
history of intestinal surgery, inflammatory bowel disease, celiac disease, lactose intolerance, chronic pancreatitis or other malabsorption disorder.
Description

Intestinal surgery | Inflammatory Bowel Disease | Celiac Disease | Lactose Intolerance | Pancreatitis, Chronic | Malabsorption Syndrome

Type de données

boolean

Alias
UMLS CUI [1]
C2064958
UMLS CUI [2]
C0021390
UMLS CUI [3]
C0007570
UMLS CUI [4]
C0022951
UMLS CUI [5]
C0149521
UMLS CUI [6]
C0024523
Retour au début de la page

Similar models

Eligibility Hypertension NCT02188381

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age >18 and <80
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
is competent and willing to provide consent
boolean
C0021430 (UMLS CUI [1])
Study Subject Group Each
Item
inclusion criteria for each subject group:
boolean
C0681850 (UMLS CUI [1,1])
C0441833 (UMLS CUI [1,2])
C1457900 (UMLS CUI [1,3])
Control Groups | Systolic Pressure | Cardiovascular Disease Absent
Item
control subjects will have a systolic bp <140mmhg with no cardiovascular disease
boolean
C0009932 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0007222 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Hypertensive disease Controlled
Item
patients with controlled hypertension
boolean
C0020538 (UMLS CUI [1,1])
C2911690 (UMLS CUI [1,2])
HYPERTENSION RESISTANT | Systolic Pressure | Antihypertensive Agents Quantity | Antihypertensive Agents Class Different
Item
resistant hypertension subjects will have systolic blood pressure (bp) ≥140 mmhg despite ≥3 anti-hypertensive medications of different classes
boolean
C0745130 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0003364 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C0003364 (UMLS CUI [4,1])
C0456387 (UMLS CUI [4,2])
C1705242 (UMLS CUI [4,3])
Study Subject Participation Status | Clinical Trial Specified
Item
subjects participating in nct 02133872 will be eligible to participate
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C0205369 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Pregnancy Recent
Item
currently pregnant or have been pregnant in the last 6 months;
boolean
C0032961 (UMLS CUI [1])
C0032961 (UMLS CUI [2,1])
C0332185 (UMLS CUI [2,2])
Antibiotic therapy Recent
Item
antibiotic treatment within 2 months of study enrollment;
boolean
C0338237 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
Antibiotics | Anti-Inflammatory Agents | Glucocorticoids | Biological Response Modifiers
Item
currently taking a medication (e.g., antibiotic, anti-inflammatory agents, glucocorticoids or other immune modulating medications);
boolean
C0003232 (UMLS CUI [1])
C0003209 (UMLS CUI [2])
C0017710 (UMLS CUI [3])
C0005525 (UMLS CUI [4])
Vitamins Discontinue Unwilling | Supplements Discontinue Unwilling | Probiotics Discontinue Unwilling | Vitamins Affecting Intestinal Microbiome | Supplements Affecting Intestinal Microbiome | Probiotics Affecting Intestinal Microbiome
Item
unwilling to discontinue vitamin or supplements, including probiotics, potentially affecting gut microbiota (vitamins/supplements and medications that possibly affect the gut microbiota should be discontinued for at least 2wks prior to stool collection);
boolean
C0042890 (UMLS CUI [1,1])
C1444662 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
C0242295 (UMLS CUI [2,1])
C1444662 (UMLS CUI [2,2])
C0558080 (UMLS CUI [2,3])
C0525033 (UMLS CUI [3,1])
C1444662 (UMLS CUI [3,2])
C0558080 (UMLS CUI [3,3])
C0042890 (UMLS CUI [4,1])
C0392760 (UMLS CUI [4,2])
C2985398 (UMLS CUI [4,3])
C0242295 (UMLS CUI [5,1])
C0392760 (UMLS CUI [5,2])
C2985398 (UMLS CUI [5,3])
C0525033 (UMLS CUI [6,1])
C0392760 (UMLS CUI [6,2])
C2985398 (UMLS CUI [6,3])
Intestinal surgery | Inflammatory Bowel Disease | Celiac Disease | Lactose Intolerance | Pancreatitis, Chronic | Malabsorption Syndrome
Item
history of intestinal surgery, inflammatory bowel disease, celiac disease, lactose intolerance, chronic pancreatitis or other malabsorption disorder.
boolean
C2064958 (UMLS CUI [1])
C0021390 (UMLS CUI [2])
C0007570 (UMLS CUI [3])
C0022951 (UMLS CUI [4])
C0149521 (UMLS CUI [5])
C0024523 (UMLS CUI [6])
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