ID

36319

Beschreibung

Universal Screening for Lynch Syndrome in Women With Endometrial and Non-Serous Ovarian Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02494791

Link

https://clinicaltrials.gov/show/NCT02494791

Stichworte

Versionen (1)
  1. 03.05.19 03.05.19 -
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See clinicaltrials.gov

Hochgeladen am

3. Mai 2019

DOI

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Creative Commons BY 4.0
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Eligibility Lynch Syndrome NCT02494791

Englisch

Eligibility Lynch Syndrome NCT02494791

1 Formulare  
Criteria
Beschreibung

Criteria

18-70 years old
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
endometrial cancer (all grades, stages and histologic subtypes except stromal sarcoma, carcinosarcoma)
Beschreibung

Endometrial Carcinoma Grade | Endometrial Carcinoma TNM clinical staging | Endometrial Carcinoma Subtype All | Exception Stromal sarcoma | Exception Carcinosarcoma

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0476089
UMLS CUI [1,2]
C0441800
UMLS CUI [2,1]
C0476089
UMLS CUI [2,2]
C3258246
UMLS CUI [3,1]
C0476089
UMLS CUI [3,2]
C0449560
UMLS CUI [3,3]
C0444868
UMLS CUI [4,1]
C1705847
UMLS CUI [4,2]
C1370723
UMLS CUI [5,1]
C1705847
UMLS CUI [5,2]
C0007140
cancer diagnosed within 6 months of consent
Beschreibung

Malignant Neoplasms

Datentyp

boolean

Alias
UMLS CUI [1]
C0006826
tumour tissue available for mmr ihc
Beschreibung

Tumor tissue sample Available Mismatch Repair | Tumor tissue sample Available Immunohistochemistry

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0475358
UMLS CUI [1,2]
C0470187
UMLS CUI [1,3]
C1155661
UMLS CUI [2,1]
C0475358
UMLS CUI [2,2]
C0470187
UMLS CUI [2,3]
C0021044
willing and able to give informed consent for participation in study
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
exclusion criteria (patients):
Beschreibung

Exclusion Criteria Patients

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0030705
patients under 18 years old or over 70 years old
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
patients with uterine adenosarcoma, leiomyosarcoma or endometrial stromal sarcoma
Beschreibung

Adenosarcoma of the uterus | Leiomyosarcoma | Endometrial Stromal Sarcoma

Datentyp

boolean

Alias
UMLS CUI [1]
C2103110
UMLS CUI [2]
C0023269
UMLS CUI [3]
C0206630
patients with pure serous or pure mucinous ovarian carcinoma
Beschreibung

Ovarian Serous Carcinoma | Ovarian mucinous carcinoma

Datentyp

boolean

Alias
UMLS CUI [1]
C1335177
UMLS CUI [2]
C1335167
patients unwilling or unable to participate in the informed consent process
Beschreibung

Informed Consent Unwilling | Informed Consent Unable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0558080
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
inclusion criteria (first-degree relatives)
Beschreibung

Inclusion criteria First Degree Relative

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C1517194
minimum 18 years old
Beschreibung

Age Minimum

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0001779
UMLS CUI [1,2]
C1524031
reside in canada
Beschreibung

Residence Canada

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0237096
UMLS CUI [1,2]
C0006823
willing and able to give informed consent for participation in study
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
exclusion criteria (first-degree relatives):
Beschreibung

Exclusion Criteria First Degree Relative

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C1517194
under 18 years old
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
reside outside of canada
Beschreibung

Residence outside Canada

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0237096
UMLS CUI [1,2]
C0205101
UMLS CUI [1,3]
C0006823
unwilling or unable to participate in the informed consent process
Beschreibung

Informed Consent Unwilling | Informed Consent Unable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0558080
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
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Ähnliche Modelle

Eligibility Lynch Syndrome NCT02494791

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Age
Item
18-70 years old
boolean
C0001779 (UMLS CUI [1])
Endometrial Carcinoma Grade | Endometrial Carcinoma TNM clinical staging | Endometrial Carcinoma Subtype All | Exception Stromal sarcoma | Exception Carcinosarcoma
Item
endometrial cancer (all grades, stages and histologic subtypes except stromal sarcoma, carcinosarcoma)
boolean
C0476089 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
C0476089 (UMLS CUI [2,1])
C3258246 (UMLS CUI [2,2])
C0476089 (UMLS CUI [3,1])
C0449560 (UMLS CUI [3,2])
C0444868 (UMLS CUI [3,3])
C1705847 (UMLS CUI [4,1])
C1370723 (UMLS CUI [4,2])
C1705847 (UMLS CUI [5,1])
C0007140 (UMLS CUI [5,2])
Malignant Neoplasms
Item
cancer diagnosed within 6 months of consent
boolean
C0006826 (UMLS CUI [1])
Tumor tissue sample Available Mismatch Repair | Tumor tissue sample Available Immunohistochemistry
Item
tumour tissue available for mmr ihc
boolean
C0475358 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
C1155661 (UMLS CUI [1,3])
C0475358 (UMLS CUI [2,1])
C0470187 (UMLS CUI [2,2])
C0021044 (UMLS CUI [2,3])
Informed Consent
Item
willing and able to give informed consent for participation in study
boolean
C0021430 (UMLS CUI [1])
Exclusion Criteria Patients
Item
exclusion criteria (patients):
boolean
C0680251 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
Age
Item
patients under 18 years old or over 70 years old
boolean
C0001779 (UMLS CUI [1])
Adenosarcoma of the uterus | Leiomyosarcoma | Endometrial Stromal Sarcoma
Item
patients with uterine adenosarcoma, leiomyosarcoma or endometrial stromal sarcoma
boolean
C2103110 (UMLS CUI [1])
C0023269 (UMLS CUI [2])
C0206630 (UMLS CUI [3])
Ovarian Serous Carcinoma | Ovarian mucinous carcinoma
Item
patients with pure serous or pure mucinous ovarian carcinoma
boolean
C1335177 (UMLS CUI [1])
C1335167 (UMLS CUI [2])
Informed Consent Unwilling | Informed Consent Unable
Item
patients unwilling or unable to participate in the informed consent process
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Inclusion criteria First Degree Relative
Item
inclusion criteria (first-degree relatives)
boolean
C1512693 (UMLS CUI [1,1])
C1517194 (UMLS CUI [1,2])
Age Minimum
Item
minimum 18 years old
boolean
C0001779 (UMLS CUI [1,1])
C1524031 (UMLS CUI [1,2])
Residence Canada
Item
reside in canada
boolean
C0237096 (UMLS CUI [1,1])
C0006823 (UMLS CUI [1,2])
Informed Consent
Item
willing and able to give informed consent for participation in study
boolean
C0021430 (UMLS CUI [1])
Exclusion Criteria First Degree Relative
Item
exclusion criteria (first-degree relatives):
boolean
C0680251 (UMLS CUI [1,1])
C1517194 (UMLS CUI [1,2])
Age
Item
under 18 years old
boolean
C0001779 (UMLS CUI [1])
Residence outside Canada
Item
reside outside of canada
boolean
C0237096 (UMLS CUI [1,1])
C0205101 (UMLS CUI [1,2])
C0006823 (UMLS CUI [1,3])
Informed Consent Unwilling | Informed Consent Unable
Item
unwilling or unable to participate in the informed consent process
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
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