ID

28367

Description

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

Link

https://clinicaltrials.gov/show/NCT01044732

Keywords

Versions (1)
  1. 1/8/18 1/8/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

January 8, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Colorectal Neoplasms NCT01044732

English

Eligibility Colorectal Neoplasms NCT01044732

1 forms  
Inclusion Criteria
Description

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;
Description

Screening colonoscopy Surveillance Resection of polyp | Screening colonoscopy Work up

Data type

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.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

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

Total colectomy

Data type

boolean

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

Inflammatory Bowel Disease

Data type

boolean

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

Polyposis

Data type

boolean

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

Stricture chronic Suspected | Exclusion Total colonoscopy

Data type

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;
Description

Diverticulitis | Megacolon, Toxic

Data type

boolean

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

Radiotherapy to abdomen | Radiotherapy to pelvis

Data type

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.
Description

Study Subject Participation Status compromises Patient safety

Data type

boolean

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

Eligibility Colorectal Neoplasms NCT01044732

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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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