ID

29043

Beschrijving

Efficacy of Lubiprostone in Combination With Standard PEG Preparation; ODM derived from: https://clinicaltrials.gov/show/NCT00689026

Link

https://clinicaltrials.gov/show/NCT00689026

Trefwoorden

Versies (1)
  1. 21-02-18 21-02-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

21 februari 2018

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Diabetes Mellitus, Type 1 NCT00689026

Engels

Eligibility Diabetes Mellitus, Type 1 NCT00689026

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with known diabetes (type i or ii) undergoing elective colonoscopy at the medical college of georgia.
Beschrijving

Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent | Colonoscopy elective

Datatype

boolean

Alias
UMLS CUI [1]
C0011854
UMLS CUI [2]
C0011860
UMLS CUI [3,1]
C0009378
UMLS CUI [3,2]
C0439608
patients aged 50 years and older.
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
women must be post-menopausal or surgically sterile.
Beschrijving

Gender | Postmenopausal state | Female Sterilization

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0232970
UMLS CUI [3]
C0015787
patients able to give a valid, informed consent.
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with impaired glucose tolerance.
Beschrijving

Impaired glucose tolerance

Datatype

boolean

Alias
UMLS CUI [1]
C0271650
patients with suspected acute or chronic pseudo-obstruction.
Beschrijving

Intestinal Pseudo-Obstruction Suspected | Chronic intestinal pseudoobstruction

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021847
UMLS CUI [1,2]
C0750491
UMLS CUI [2]
C1864223
patients with active gastrointestinal bleeding.
Beschrijving

Gastrointestinal Hemorrhage

Datatype

boolean

Alias
UMLS CUI [1]
C0017181
patients with known inflammatory bowel disease.
Beschrijving

Inflammatory Bowel Disease

Datatype

boolean

Alias
UMLS CUI [1]
C0021390
patients with chronic diarrhea.
Beschrijving

Chronic diarrhea

Datatype

boolean

Alias
UMLS CUI [1]
C0401151
patients with prior colonic resection.
Beschrijving

Excision Colon

Datatype

boolean

Alias
UMLS CUI [1,1]
C0728940
UMLS CUI [1,2]
C1281569
patients with active diverticulitis.
Beschrijving

Diverticulitis

Datatype

boolean

Alias
UMLS CUI [1]
C0012813
patients with a known colonic mass.
Beschrijving

Colonic Mass

Datatype

boolean

Alias
UMLS CUI [1]
C3887631
patients with clinical evidence of decompensated liver disease.
Beschrijving

Decompensated liver disease

Datatype

boolean

Alias
UMLS CUI [1]
C4075847
patients with clinical evidence of decompensated renal disease or patients on dialysis.
Beschrijving

Kidney Disease Decompensated | Dialysis

Datatype

boolean

Alias
UMLS CUI [1,1]
C0022658
UMLS CUI [1,2]
C0205434
UMLS CUI [2]
C0011946
patients currently or previously taking lubiprostone.
Beschrijving

lubiprostone

Datatype

boolean

Alias
UMLS CUI [1]
C1684405
patients with an allergy to lubiprostone.
Beschrijving

Hypersensitivity lubiprostone

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1684405
Terug naar het begin van de pagina

Similar models

Eligibility Diabetes Mellitus, Type 1 NCT00689026

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent | Colonoscopy elective
Item
patients with known diabetes (type i or ii) undergoing elective colonoscopy at the medical college of georgia.
boolean
C0011854 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
C0009378 (UMLS CUI [3,1])
C0439608 (UMLS CUI [3,2])
Age
Item
patients aged 50 years and older.
boolean
C0001779 (UMLS CUI [1])
Gender | Postmenopausal state | Female Sterilization
Item
women must be post-menopausal or surgically sterile.
boolean
C0079399 (UMLS CUI [1])
C0232970 (UMLS CUI [2])
C0015787 (UMLS CUI [3])
Informed Consent
Item
patients able to give a valid, informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Impaired glucose tolerance
Item
patients with impaired glucose tolerance.
boolean
C0271650 (UMLS CUI [1])
Intestinal Pseudo-Obstruction Suspected | Chronic intestinal pseudoobstruction
Item
patients with suspected acute or chronic pseudo-obstruction.
boolean
C0021847 (UMLS CUI [1,1])
C0750491 (UMLS CUI [1,2])
C1864223 (UMLS CUI [2])
Gastrointestinal Hemorrhage
Item
patients with active gastrointestinal bleeding.
boolean
C0017181 (UMLS CUI [1])
Inflammatory Bowel Disease
Item
patients with known inflammatory bowel disease.
boolean
C0021390 (UMLS CUI [1])
Chronic diarrhea
Item
patients with chronic diarrhea.
boolean
C0401151 (UMLS CUI [1])
Excision Colon
Item
patients with prior colonic resection.
boolean
C0728940 (UMLS CUI [1,1])
C1281569 (UMLS CUI [1,2])
Diverticulitis
Item
patients with active diverticulitis.
boolean
C0012813 (UMLS CUI [1])
Colonic Mass
Item
patients with a known colonic mass.
boolean
C3887631 (UMLS CUI [1])
Decompensated liver disease
Item
patients with clinical evidence of decompensated liver disease.
boolean
C4075847 (UMLS CUI [1])
Kidney Disease Decompensated | Dialysis
Item
patients with clinical evidence of decompensated renal disease or patients on dialysis.
boolean
C0022658 (UMLS CUI [1,1])
C0205434 (UMLS CUI [1,2])
C0011946 (UMLS CUI [2])
lubiprostone
Item
patients currently or previously taking lubiprostone.
boolean
C1684405 (UMLS CUI [1])
Hypersensitivity lubiprostone
Item
patients with an allergy to lubiprostone.
boolean
C0020517 (UMLS CUI [1,1])
C1684405 (UMLS CUI [1,2])
Terug naar het begin van de pagina 

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