Information:
Fel:
ID
24793
Beskrivning
Cobiprostone Prevention of NSAID-induced Gastroduodenal Injury; ODM derived from: https://clinicaltrials.gov/show/NCT00597818
Länk
https://clinicaltrials.gov/show/NCT00597818
Nyckelord
Versioner (2)
- 2017-08-17 2017-08-17 -
- 2017-08-17 2017-08-17 -
Uppladdad den
17 augusti 2017
DOI
För en begäran logga in.
Licens
Creative Commons BY 4.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
Eligibility NSAID-induced Gastroduodenal Injury NCT00597818
Eligibility NSAID-induced Gastroduodenal Injury NCT00597818
- StudyEvent: Eligibility
Similar models
Eligibility NSAID-induced Gastroduodenal Injury NCT00597818
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Age
Item
patient is more than 40 and less than 70 years of age.
boolean
C0001779 (UMLS CUI [1])
Osteoarthritis | Rheumatoid Arthritis | Benefit Due to NSAID treatment
Item
patient has confirmed osteoarthritis (oa) and/or rheumatoid arthritis (ra) and could benefit from nsaid therapy.
boolean
C0029408 (UMLS CUI [1])
C0003873 (UMLS CUI [2])
C0814225 (UMLS CUI [3,1])
C0678226 (UMLS CUI [3,2])
C0746950 (UMLS CUI [3,3])
C0003873 (UMLS CUI [2])
C0814225 (UMLS CUI [3,1])
C0678226 (UMLS CUI [3,2])
C0746950 (UMLS CUI [3,3])
Helicobacter pylori gastrointestinal tract infection Absent
Item
no current gastrointestinal h. pylori infection.
boolean
C0585625 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Allergy to nonsteroidal anti-inflammatory agents | Medical contraindication NSAID treatment
Item
known allergy or hypersensitivity to nsaids, or has any other contraindicated condition(s) to nsaid therapy.
boolean
C0746949 (UMLS CUI [1])
C1301624 (UMLS CUI [2,1])
C0746950 (UMLS CUI [2,2])
C1301624 (UMLS CUI [2,1])
C0746950 (UMLS CUI [2,2])
Gastrointestinal Surgical Procedure | Abdominal operation | Bowel resection
Item
patient has undergone a gastrointestinal or abdominal surgical procedure within 90 days prior to the screening visit, or has had a bowel resection at any time.
boolean
C0524722 (UMLS CUI [1])
C0198482 (UMLS CUI [2])
C0741614 (UMLS CUI [3])
C0198482 (UMLS CUI [2])
C0741614 (UMLS CUI [3])
Gastrointestinal complication | Gastrointestinal Diseases | Barrett Esophagus | Erosive esophagitis | Esophageal Stenosis | Esophageal ring | Obstruction gastric | Irritable Bowel Syndrome | Inflammatory Bowel Disease
Item
medical history includes prior or active gi complications and/or disorders, including but not limited to barrett's esophagus, erosive esophagitis, esophageal stricture or ring, gastric obstruction, irritable bowel syndrome (ibs), or inflammatory bowel disease (ibd).
boolean
C0161819 (UMLS CUI [1])
C0017178 (UMLS CUI [2])
C0004763 (UMLS CUI [3])
C0267055 (UMLS CUI [4])
C0014866 (UMLS CUI [5])
C0267081 (UMLS CUI [6])
C0149700 (UMLS CUI [7])
C0022104 (UMLS CUI [8])
C0021390 (UMLS CUI [9])
C0017178 (UMLS CUI [2])
C0004763 (UMLS CUI [3])
C0267055 (UMLS CUI [4])
C0014866 (UMLS CUI [5])
C0267081 (UMLS CUI [6])
C0149700 (UMLS CUI [7])
C0022104 (UMLS CUI [8])
C0021390 (UMLS CUI [9])
Peptic Ulcer Symptomatic | Gastrointestinal Hemorrhage
Item
active symptomatic peptic ulcer disease or gi bleeding.
boolean
C0030920 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0017181 (UMLS CUI [2])
C0231220 (UMLS CUI [1,2])
C0017181 (UMLS CUI [2])
cobiprostone | SPI-8811 | Amitiza | lubiprostone | SPI 0211 | RU 0211
Item
patient has received cobiprostone (spi-8811; ru-8811) or amitiza (lubiprostone, spi-0211, or ru-0211) at any time prior to participation in this study.
boolean
C2699393 (UMLS CUI [1])
C2703103 (UMLS CUI [2])
C1699150 (UMLS CUI [3])
C1684405 (UMLS CUI [4])
C1681887 (UMLS CUI [5])
C1683269 (UMLS CUI [6])
C2703103 (UMLS CUI [2])
C1699150 (UMLS CUI [3])
C1684405 (UMLS CUI [4])
C1681887 (UMLS CUI [5])
C1683269 (UMLS CUI [6])