ID

31244

Description

Changes in Ectopic Fat Following Surgically Induced Weight Loss; ODM derived from: https://clinicaltrials.gov/show/NCT00840307

Lien

https://clinicaltrials.gov/show/NCT00840307

Mots-clés

Versions (1)
  1. 01/08/2018 01/08/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

1 août 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Obesity NCT00840307

Anglais

Eligibility Obesity NCT00840307

1 Formulaires  
  1. StudyEvent: Eligibility
    1. Eligibility Obesity NCT00840307
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
greater than 18 years old
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
fully understanding and willing to undergo study procedures
Description

Comprehension Study Protocol | Protocol Compliance

Type de données

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C2348563
UMLS CUI [2]
C0525058
available for follow-up
Description

Patient Available Follow-up

Type de données

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0470187
UMLS CUI [1,3]
C3274571
understand and willing to sign informed consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
pharmacologic agents with the potential to change ectopic fat content (i.e. pioglitazone) are allowed if the patient has been on a stable dose for at least 3 months and plans to continue the same dose for the duration of the study
Description

Pharmaceutical Preparations Changing Fat Contents | Pioglitazone | Pharmaceutical Preparations Dose Stable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0392747
UMLS CUI [1,3]
C0015677
UMLS CUI [1,4]
C0456205
UMLS CUI [2]
C0071097
UMLS CUI [3,1]
C0013227
UMLS CUI [3,2]
C0178602
UMLS CUI [3,3]
C0205360
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
contraindication to mri (i.e. metallic implants, severe claustrophobia, weight above 320lb)
Description

Medical contraindication MRI | Claustrophobia Severe | Body Weight Pounds Quantity

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
UMLS CUI [2,1]
C0008909
UMLS CUI [2,2]
C0205082
UMLS CUI [3,1]
C0005910
UMLS CUI [3,2]
C0439219
UMLS CUI [3,3]
C1265611
contraindication to phlebotomy (i.e. no accessible veins, hemoglobin <10 mg/dl)
Description

Medical contraindication Venesection | Access Veins Lacking | Hemoglobin measurement

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0684257
UMLS CUI [2,1]
C0444454
UMLS CUI [2,2]
C0042449
UMLS CUI [2,3]
C0332268
UMLS CUI [3]
C0518015
history of pancreatic disease other than diabetes
Description

Pancreatic Disease | Exception Diabetes Mellitus

Type de données

boolean

Alias
UMLS CUI [1]
C0030286
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0011849
regular use of more than 2 alcoholic drinks per day
Description

Consumption Alcoholic drinks Number per day

Type de données

boolean

Alias
UMLS CUI [1,1]
C0001948
UMLS CUI [1,2]
C0001967
UMLS CUI [1,3]
C0237753
UMLS CUI [1,4]
C0439505
pregnancy
Description

Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
non-english speaking
Description

Lacking Able to speak English Language

Type de données

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C0564215
UMLS CUI [1,3]
C0376245
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Similar models

Eligibility Obesity NCT00840307

1 Formulaires
  1. StudyEvent: Eligibility
    1. Eligibility Obesity NCT00840307
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
greater than 18 years old
boolean
C0001779 (UMLS CUI [1])
Comprehension Study Protocol | Protocol Compliance
Item
fully understanding and willing to undergo study procedures
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2])
Patient Available Follow-up
Item
available for follow-up
boolean
C0030705 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,3])
Informed Consent
Item
understand and willing to sign informed consent
boolean
C0021430 (UMLS CUI [1])
Pharmaceutical Preparations Changing Fat Contents | Pioglitazone | Pharmaceutical Preparations Dose Stable
Item
pharmacologic agents with the potential to change ectopic fat content (i.e. pioglitazone) are allowed if the patient has been on a stable dose for at least 3 months and plans to continue the same dose for the duration of the study
boolean
C0013227 (UMLS CUI [1,1])
C0392747 (UMLS CUI [1,2])
C0015677 (UMLS CUI [1,3])
C0456205 (UMLS CUI [1,4])
C0071097 (UMLS CUI [2])
C0013227 (UMLS CUI [3,1])
C0178602 (UMLS CUI [3,2])
C0205360 (UMLS CUI [3,3])
Item Group
C0680251 (UMLS CUI)
Medical contraindication MRI | Claustrophobia Severe | Body Weight Pounds Quantity
Item
contraindication to mri (i.e. metallic implants, severe claustrophobia, weight above 320lb)
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C0008909 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0005910 (UMLS CUI [3,1])
C0439219 (UMLS CUI [3,2])
C1265611 (UMLS CUI [3,3])
Medical contraindication Venesection | Access Veins Lacking | Hemoglobin measurement
Item
contraindication to phlebotomy (i.e. no accessible veins, hemoglobin <10 mg/dl)
boolean
C1301624 (UMLS CUI [1,1])
C0684257 (UMLS CUI [1,2])
C0444454 (UMLS CUI [2,1])
C0042449 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])
C0518015 (UMLS CUI [3])
Pancreatic Disease | Exception Diabetes Mellitus
Item
history of pancreatic disease other than diabetes
boolean
C0030286 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0011849 (UMLS CUI [2,2])
Consumption Alcoholic drinks Number per day
Item
regular use of more than 2 alcoholic drinks per day
boolean
C0001948 (UMLS CUI [1,1])
C0001967 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,3])
C0439505 (UMLS CUI [1,4])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Lacking Able to speak English Language
Item
non-english speaking
boolean
C0332268 (UMLS CUI [1,1])
C0564215 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
Retour au début de la page 

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