ID

20606

Description

Effect of Androgel on Type 2 Diabetic Males With Hypogonadism; ODM derived from: https://clinicaltrials.gov/show/NCT00350701

Lien

https://clinicaltrials.gov/show/NCT00350701

Mots-clés

  1. 06/03/2017 06/03/2017 -
Téléchargé le

6 mars 2017

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.

Groupe Item commentaires pour :

Item commentaires pour :

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

Eligibility Diabetes Mellitus Type 2 NCT00350701

Eligibility Diabetes Mellitus Type 2 NCT00350701

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
males with age 35-75 years inclusive.
Description

Gender | Age

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
evidence of hypogonadism: low free testosterone.
Description

Hypogonadism Evidence of | Blood testosterone free decreased

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020619
UMLS CUI [1,2]
C0332120
UMLS CUI [2]
C1096126
type 2 diabetes
Description

Diabetes Mellitus, Non-Insulin-Dependent

Type de données

boolean

Alias
UMLS CUI [1]
C0011860
people on stable doses of cholesterol lowering medications, blood pressure medications and multi-vitamins are allowed.
Description

Anticholesteremic Agents Dose Stable | Blood Pressure Pharmaceutical Preparations | Multivitamin preparation

Type de données

boolean

Alias
UMLS CUI [1,1]
C0003277
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0205360
UMLS CUI [2,1]
C0005823
UMLS CUI [2,2]
C0013227
UMLS CUI [3]
C0301532
if currently on testosterone replacement,testosterone treatment will be held for 8 weeks.
Description

Testosterone Replacement | Testosterone Maintenance Duration

Type de données

boolean

Alias
UMLS CUI [1,1]
C0039601
UMLS CUI [1,2]
C0559956
UMLS CUI [2,1]
C0039601
UMLS CUI [2,2]
C0024501
UMLS CUI [2,3]
C0449238
bp under control even if on medication.
Description

Blood Pressure Controlled | Taking medication

Type de données

boolean

Alias
UMLS CUI [1,1]
C0005823
UMLS CUI [1,2]
C2587213
UMLS CUI [2]
C1290952
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
coronary event or procedure in previous past 4 wks.
Description

Event Coronary | Procedures on Coronary Arteries

Type de données

boolean

Alias
UMLS CUI [1,1]
C0441471
UMLS CUI [1,2]
C1522318
UMLS CUI [2]
C0869781
high psa
Description

Raised prostate specific antigen

Type de données

boolean

Alias
UMLS CUI [1]
C0178415
h/o prostate cancer
Description

Prostate carcinoma

Type de données

boolean

Alias
UMLS CUI [1]
C0600139
hepatic or renal disease
Description

Liver disease | Kidney Disease

Type de données

boolean

Alias
UMLS CUI [1]
C0023895
UMLS CUI [2]
C0022658
participation in any other concurrent clinical trial
Description

Study Subject Participation Status

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
any other life- threatening , non cardiac disease.
Description

Life threatening illness | Heart Disease

Type de données

boolean

Alias
UMLS CUI [1]
C3846017
UMLS CUI [2]
C0018799
uncontrolled bp
Description

Blood Pressure Uncontrolled

Type de données

boolean

Alias
UMLS CUI [1,1]
C0005823
UMLS CUI [1,2]
C0205318
congestive heart failure
Description

Congestive heart failure

Type de données

boolean

Alias
UMLS CUI [1]
C0018802
high hemoglobin
Description

Hemoglobin increased

Type de données

boolean

Alias
UMLS CUI [1]
C0549448
use of investigational agent or therapeutic regimen within 30 days of study.
Description

Investigational New Drugs | Therapies, Investigational

Type de données

boolean

Alias
UMLS CUI [1]
C0013230
UMLS CUI [2]
C0949266

Similar models

Eligibility Diabetes Mellitus Type 2 NCT00350701

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Age
Item
males with age 35-75 years inclusive.
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Hypogonadism Evidence of | Blood testosterone free decreased
Item
evidence of hypogonadism: low free testosterone.
boolean
C0020619 (UMLS CUI [1,1])
C0332120 (UMLS CUI [1,2])
C1096126 (UMLS CUI [2])
Diabetes Mellitus, Non-Insulin-Dependent
Item
type 2 diabetes
boolean
C0011860 (UMLS CUI [1])
Anticholesteremic Agents Dose Stable | Blood Pressure Pharmaceutical Preparations | Multivitamin preparation
Item
people on stable doses of cholesterol lowering medications, blood pressure medications and multi-vitamins are allowed.
boolean
C0003277 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0005823 (UMLS CUI [2,1])
C0013227 (UMLS CUI [2,2])
C0301532 (UMLS CUI [3])
Testosterone Replacement | Testosterone Maintenance Duration
Item
if currently on testosterone replacement,testosterone treatment will be held for 8 weeks.
boolean
C0039601 (UMLS CUI [1,1])
C0559956 (UMLS CUI [1,2])
C0039601 (UMLS CUI [2,1])
C0024501 (UMLS CUI [2,2])
C0449238 (UMLS CUI [2,3])
Blood Pressure Controlled | Taking medication
Item
bp under control even if on medication.
boolean
C0005823 (UMLS CUI [1,1])
C2587213 (UMLS CUI [1,2])
C1290952 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Event Coronary | Procedures on Coronary Arteries
Item
coronary event or procedure in previous past 4 wks.
boolean
C0441471 (UMLS CUI [1,1])
C1522318 (UMLS CUI [1,2])
C0869781 (UMLS CUI [2])
Raised prostate specific antigen
Item
high psa
boolean
C0178415 (UMLS CUI [1])
Prostate carcinoma
Item
h/o prostate cancer
boolean
C0600139 (UMLS CUI [1])
Liver disease | Kidney Disease
Item
hepatic or renal disease
boolean
C0023895 (UMLS CUI [1])
C0022658 (UMLS CUI [2])
Study Subject Participation Status
Item
participation in any other concurrent clinical trial
boolean
C2348568 (UMLS CUI [1])
Life threatening illness | Heart Disease
Item
any other life- threatening , non cardiac disease.
boolean
C3846017 (UMLS CUI [1])
C0018799 (UMLS CUI [2])
Blood Pressure Uncontrolled
Item
uncontrolled bp
boolean
C0005823 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Congestive heart failure
Item
congestive heart failure
boolean
C0018802 (UMLS CUI [1])
Hemoglobin increased
Item
high hemoglobin
boolean
C0549448 (UMLS CUI [1])
Investigational New Drugs | Therapies, Investigational
Item
use of investigational agent or therapeutic regimen within 30 days of study.
boolean
C0013230 (UMLS CUI [1])
C0949266 (UMLS CUI [2])

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

Les champs marqués d’un * sont obligatoires.

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