Informationen:
Fehler:
ID
29043
Beschreibung
Efficacy of Lubiprostone in Combination With Standard PEG Preparation; ODM derived from: https://clinicaltrials.gov/show/NCT00689026
Link
https://clinicaltrials.gov/show/NCT00689026
Stichworte
Versionen (1)
- 21.02.18 21.02.18 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
21. Februar 2018
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY 4.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Eligibility Diabetes Mellitus, Type 1 NCT00689026
Eligibility Diabetes Mellitus, Type 1 NCT00689026
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Diabetes Mellitus, Type 1 NCT00689026
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
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])
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])
C0232970 (UMLS CUI [2])
C0015787 (UMLS CUI [3])
Informed Consent
Item
patients able to give a valid, informed consent.
boolean
C0021430 (UMLS CUI [1])
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])
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])
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])
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])
C1684405 (UMLS CUI [1,2])