ID

28367

Beschrijving

Third Eye Retroscope Randomized Clinical Evaluation; ODM derived from: https://clinicaltrials.gov/show/NCT01044732

Link

https://clinicaltrials.gov/show/NCT01044732

Trefwoorden

  1. 08-01-18 08-01-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

8 januari 2018

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Colorectal Neoplasms NCT01044732

Eligibility Colorectal Neoplasms NCT01044732

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
the patient is undergoing colonoscopy for screening, for surveillance in follow-up of previous polypectomy or for diagnostic workup;
Beschrijving

Screening colonoscopy Surveillance Resection of polyp | Screening colonoscopy Work up

Datatype

boolean

Alias
UMLS CUI [1,1]
C1882982
UMLS CUI [1,2]
C0038842
UMLS CUI [1,3]
C0521210
UMLS CUI [2,1]
C1882982
UMLS CUI [2,2]
C0750430
the patient must understand and provide written consent for the procedure.
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with a history of colonic resection;
Beschrijving

Total colectomy

Datatype

boolean

Alias
UMLS CUI [1]
C0192871
patients with inflammatory bowel disease;
Beschrijving

Inflammatory Bowel Disease

Datatype

boolean

Alias
UMLS CUI [1]
C0021390
patients with a personal history of polyposis syndrome;
Beschrijving

Polyposis

Datatype

boolean

Alias
UMLS CUI [1]
C0334108
patients with suspected chronic stricture potentially precluding complete colonoscopy;
Beschrijving

Stricture chronic Suspected | Exclusion Total colonoscopy

Datatype

boolean

Alias
UMLS CUI [1,1]
C1261287
UMLS CUI [1,2]
C0205191
UMLS CUI [1,3]
C0750491
UMLS CUI [2,1]
C2828389
UMLS CUI [2,2]
C0009556
patients with diverticulitis or toxic megacolon;
Beschrijving

Diverticulitis | Megacolon, Toxic

Datatype

boolean

Alias
UMLS CUI [1]
C0012813
UMLS CUI [2]
C0025162
patients with a history of radiation therapy to abdomen or pelvis;
Beschrijving

Radiotherapy to abdomen | Radiotherapy to pelvis

Datatype

boolean

Alias
UMLS CUI [1]
C1997554
UMLS CUI [2]
C1536155
patients who are currently enrolled in another clinical investigation in which the intervention might compromise the safety of the patient's participation in this study.
Beschrijving

Study Subject Participation Status compromises Patient safety

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C2945640
UMLS CUI [1,3]
C1113679

Similar models

Eligibility Colorectal Neoplasms NCT01044732

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Screening colonoscopy Surveillance Resection of polyp | Screening colonoscopy Work up
Item
the patient is undergoing colonoscopy for screening, for surveillance in follow-up of previous polypectomy or for diagnostic workup;
boolean
C1882982 (UMLS CUI [1,1])
C0038842 (UMLS CUI [1,2])
C0521210 (UMLS CUI [1,3])
C1882982 (UMLS CUI [2,1])
C0750430 (UMLS CUI [2,2])
Informed Consent
Item
the patient must understand and provide written consent for the procedure.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Total colectomy
Item
patients with a history of colonic resection;
boolean
C0192871 (UMLS CUI [1])
Inflammatory Bowel Disease
Item
patients with inflammatory bowel disease;
boolean
C0021390 (UMLS CUI [1])
Polyposis
Item
patients with a personal history of polyposis syndrome;
boolean
C0334108 (UMLS CUI [1])
Stricture chronic Suspected | Exclusion Total colonoscopy
Item
patients with suspected chronic stricture potentially precluding complete colonoscopy;
boolean
C1261287 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
C0750491 (UMLS CUI [1,3])
C2828389 (UMLS CUI [2,1])
C0009556 (UMLS CUI [2,2])
Diverticulitis | Megacolon, Toxic
Item
patients with diverticulitis or toxic megacolon;
boolean
C0012813 (UMLS CUI [1])
C0025162 (UMLS CUI [2])
Radiotherapy to abdomen | Radiotherapy to pelvis
Item
patients with a history of radiation therapy to abdomen or pelvis;
boolean
C1997554 (UMLS CUI [1])
C1536155 (UMLS CUI [2])
Study Subject Participation Status compromises Patient safety
Item
patients who are currently enrolled in another clinical investigation in which the intervention might compromise the safety of the patient's participation in this study.
boolean
C2348568 (UMLS CUI [1,1])
C2945640 (UMLS CUI [1,2])
C1113679 (UMLS CUI [1,3])

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