ID

28178

Beschreibung

Efficacy of the Third Eye Retroscope Auxiliary Imaging System; ODM derived from: https://clinicaltrials.gov/show/NCT00657371

Link

https://clinicaltrials.gov/show/NCT00657371

Stichworte

Versionen (1)
  1. 27.12.17 27.12.17 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

27. Dezember 2017

DOI

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Creative Commons BY 4.0
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Eligibility Colorectal Cancer NCT00657371

Englisch

Eligibility Colorectal Cancer NCT00657371

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
the patient is undergoing colonoscopy for screening purposes or for surveillance in follow-up for previous polypectomy.
Beschreibung

Colonoscopy Screening | Colonoscopy Surveillance Resection of polyp

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0009378
UMLS CUI [1,2]
C1305399
UMLS CUI [2,1]
C0009378
UMLS CUI [2,2]
C0220920
UMLS CUI [2,3]
C0521210
the patient is at satisfactory risk for abdominal surgery.
Beschreibung

At risk Operation on abdominal region

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1444641
UMLS CUI [1,2]
C0198482
the patient must understand and provide written consent for the procedure.
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who are <50 years or >80 years of age
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
patients who are pregnant.
Beschreibung

Pregnancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
patients with history of colonic resection.
Beschreibung

Excision Colonic

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0728940
UMLS CUI [1,2]
C0009368
patients requiring ongoing anticoagulation therapy.
Beschreibung

Anticoagulation Therapy Patient need for

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0003281
UMLS CUI [1,2]
C0686904
patients with a history of severe cardiovascular, pulmonary, liver or renal disease.
Beschreibung

Cardiovascular Disease Severe | Lung disease Severe | Liver disease Severe | Kidney Disease Severe

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0007222
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0024115
UMLS CUI [2,2]
C0205082
UMLS CUI [3,1]
C0023895
UMLS CUI [3,2]
C0205082
UMLS CUI [4,1]
C0022658
UMLS CUI [4,2]
C0205082
patients with hypersensitivity to opioid analgesics.
Beschreibung

Hypersensitivity Opioid Analgesics

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0002772
patients with an active systemic infection.
Beschreibung

Sepsis

Datentyp

boolean

Alias
UMLS CUI [1]
C0243026
patients with suspected chronic stricture potentially precluding complete colonoscopy.
Beschreibung

Stenosis chronic Suspected | Total colonoscopy Excluded potential

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1261287
UMLS CUI [1,2]
C0205191
UMLS CUI [1,3]
C0750491
UMLS CUI [2,1]
C0009556
UMLS CUI [2,2]
C0332196
UMLS CUI [2,3]
C3245505
patients with major psychiatric disease (dementia, schizophrenia or depression).
Beschreibung

Mental disorder Major | Dementia | Schizophrenia | Depressive disorder

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0004936
UMLS CUI [1,2]
C0205164
UMLS CUI [2]
C0497327
UMLS CUI [3]
C0036341
UMLS CUI [4]
C0011581
patients with diverticulitis or toxic megacolon.
Beschreibung

Diverticulitis | Megacolon, Toxic

Datentyp

boolean

Alias
UMLS CUI [1]
C0012813
UMLS CUI [2]
C0025162
patients with history of radiation therapy to abdomen or pelvis.
Beschreibung

Radiotherapy to abdomen | Radiotherapy to pelvis

Datentyp

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.
Beschreibung

Study Subject Participation Status | Intervention compromises Patient safety

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0184661
UMLS CUI [2,2]
C2945640
UMLS CUI [2,3]
C1113679
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Ähnliche Modelle

Eligibility Colorectal Cancer NCT00657371

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Colonoscopy Screening | Colonoscopy Surveillance Resection of polyp
Item
the patient is undergoing colonoscopy for screening purposes or for surveillance in follow-up for previous polypectomy.
boolean
C0009378 (UMLS CUI [1,1])
C1305399 (UMLS CUI [1,2])
C0009378 (UMLS CUI [2,1])
C0220920 (UMLS CUI [2,2])
C0521210 (UMLS CUI [2,3])
At risk Operation on abdominal region
Item
the patient is at satisfactory risk for abdominal surgery.
boolean
C1444641 (UMLS CUI [1,1])
C0198482 (UMLS CUI [1,2])
Informed Consent
Item
the patient must understand and provide written consent for the procedure.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Age
Item
patients who are <50 years or >80 years of age
boolean
C0001779 (UMLS CUI [1])
Pregnancy
Item
patients who are pregnant.
boolean
C0032961 (UMLS CUI [1])
Excision Colonic
Item
patients with history of colonic resection.
boolean
C0728940 (UMLS CUI [1,1])
C0009368 (UMLS CUI [1,2])
Anticoagulation Therapy Patient need for
Item
patients requiring ongoing anticoagulation therapy.
boolean
C0003281 (UMLS CUI [1,1])
C0686904 (UMLS CUI [1,2])
Cardiovascular Disease Severe | Lung disease Severe | Liver disease Severe | Kidney Disease Severe
Item
patients with a history of severe cardiovascular, pulmonary, liver or renal disease.
boolean
C0007222 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0024115 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0023895 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0022658 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
Hypersensitivity Opioid Analgesics
Item
patients with hypersensitivity to opioid analgesics.
boolean
C0020517 (UMLS CUI [1,1])
C0002772 (UMLS CUI [1,2])
Sepsis
Item
patients with an active systemic infection.
boolean
C0243026 (UMLS CUI [1])
Stenosis chronic Suspected | Total colonoscopy Excluded potential
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])
C0009556 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C3245505 (UMLS CUI [2,3])
Mental disorder Major | Dementia | Schizophrenia | Depressive disorder
Item
patients with major psychiatric disease (dementia, schizophrenia or depression).
boolean
C0004936 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C0497327 (UMLS CUI [2])
C0036341 (UMLS CUI [3])
C0011581 (UMLS CUI [4])
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 history of radiation therapy to abdomen or pelvis.
boolean
C1997554 (UMLS CUI [1])
C1536155 (UMLS CUI [2])
Study Subject Participation Status | Intervention 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])
C0184661 (UMLS CUI [2,1])
C2945640 (UMLS CUI [2,2])
C1113679 (UMLS CUI [2,3])
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