ID

36319

Beschrijving

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

Trefwoorden

Versies (1)
  1. 03-05-19 03-05-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

3 mei 2019

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Lynch Syndrome NCT02494791

Engels

Eligibility Lynch Syndrome NCT02494791

1 Formulieren  
Criteria
Beschrijving

Criteria

18-70 years old
Beschrijving

Age

Datatype

boolean

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

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

Datatype

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
Beschrijving

Malignant Neoplasms

Datatype

boolean

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

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

Datatype

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
Beschrijving

Informed Consent

Datatype

boolean

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

Exclusion Criteria Patients

Datatype

boolean

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

Age

Datatype

boolean

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

Adenosarcoma of the uterus | Leiomyosarcoma | Endometrial Stromal Sarcoma

Datatype

boolean

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

Ovarian Serous Carcinoma | Ovarian mucinous carcinoma

Datatype

boolean

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

Informed Consent Unwilling | Informed Consent Unable

Datatype

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)
Beschrijving

Inclusion criteria First Degree Relative

Datatype

boolean

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

Age Minimum

Datatype

boolean

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

Residence Canada

Datatype

boolean

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

Informed Consent

Datatype

boolean

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

Exclusion Criteria First Degree Relative

Datatype

boolean

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

Age

Datatype

boolean

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

Residence outside Canada

Datatype

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
Beschrijving

Informed Consent Unwilling | Informed Consent Unable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0558080
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
Terug naar het begin van de pagina

Similar models

Eligibility Lynch Syndrome NCT02494791

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial