0 Avaliações

ID

44770

Descrição

Lymphatic Mapping, Sentinel Lymph Node Analysis, and Blood Tests in Detecting and Predicting Early Micrometastases in Patients With Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00625625

Link

https://clinicaltrials.gov/show/NCT00625625

Palavras-chave

  1. 18/08/2016 18/08/2016 -
  2. 13/04/2021 13/04/2021 - Dr. rer. medic Philipp Neuhaus
  3. 17/11/2021 17/11/2021 -
Titular dos direitos

John Wayne Cancer Institute

Transferido a

17 de novembro de 2021

DOI

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Licença

Creative Commons BY 4.0

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    Eligibility Colorectal Cancer NCT00625625

    Eligibility Colorectal Cancer NCT00625625

    Criteria
    Descrição

    Criteria

    diagnosis of colorectal cancer as detected by proctosigmoidoscopy, flexible endoscopy, or gastrografin/barium enema
    Descrição

    diagnosis of colorectal cancer

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0011900 (Diagnosis)
    SNOMED
    439401001
    LOINC
    LP30831-9
    UMLS CUI [1,2]
    C0009402 (Colorectal Carcinoma)
    LOINC
    LA15686-1
    no evidence of distant metastases by ct scan of the abdomen and pelvis and chest x-ray or ct scan of the chest performed within 6 weeks prior to enrollment
    Descrição

    distant metastases

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C3258247 (TNM clinical staging - distant metastases - M)
    LOINC
    LP130440-3
    preoperative ct scans and testing showing non-specific or non-diagnostic (equivocal) abnormalities may be eligible pending intraoperative exploration
    Descrição

    preoperative diagnostics

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C1318968 (Pre-op diagnosis)
    SNOMED
    406520001
    no discovery of distant metastases intra-operatively
    Descrição

    no discovery of distant metastases intra-operatively

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0027627 (Neoplasm Metastasis)
    LOINC
    LP35033-7
    UMLS CUI [1,2]
    C0243164 (peroperative procedures)
    patient characteristics:
    Descrição

    patient characteristics

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0815172 (Client Characteristics)
    ecog performance status (ps) or zubrod ps equal to 2
    Descrição

    ecog performance status or zubrod performance status

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C1520224 (ECOG performance status)
    SNOMED
    423740007
    UMLS CUI [2]
    C3714786 (Zubrod Performance Status)
    life expectancy > 5 years not including the disease/diagnosis of colorectal cancer
    Descrição

    life expectancy

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0023671 (Life Expectancy)
    not pregnant or nursing
    Descrição

    pregnant or nursing

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0032961 (Pregnancy)
    SNOMED
    289908002
    LOINC
    LP75920-6
    UMLS CUI [2]
    C0006147 (Breast Feeding)
    SNOMED
    169741004
    LOINC
    LP420040-0
    negative pregnancy test
    Descrição

    negative pregnancy test

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0427780 (Pregnancy test negative)
    SNOMED
    250425007
    fertile patients must use effective contraception
    Descrição

    contraceptive methods

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0700589 (Contraceptive methods)
    SNOMED
    13197004
    no requirement for emergent surgery (within 2 hours of presentation) to prevent a life-threatening situation or death including:
    Descrição

    emergency surgery

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C2216322 (emergency surgical procedure)
    perforated colon
    Descrição

    perforated colon

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0347646 (Perforation of colon)
    SNOMED
    50257008
    metabolically significant complete bowel obstruction
    Descrição

    complete bowel obstruction

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0021843 (Intestinal Obstruction)
    SNOMED
    81060008
    UMLS CUI [1,2]
    C0205197 (Complete)
    SNOMED
    255594003
    LOINC
    LA13937-0
    massive gi bleeding
    Descrição

    gi bleeding

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0017181 (Gastrointestinal Hemorrhage)
    SNOMED
    74474003
    LOINC
    LP209002-7
    UMLS CUI [1,2]
    C0522501 (Massive)
    SNOMED
    46998006
    LOINC
    LA17968-1
    occult bleeding or early or partial bowel obstruction not requiring emergent surgery allowed
    Descrição

    occult bleeding, partial bowel obstruction, emergency surgery

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0333282 (Occult hemorrhage)
    SNOMED
    46386005
    UMLS CUI [2]
    C1328480 (Partial obstruction of intestine)
    SNOMED
    16834011000119109
    UMLS CUI [3]
    C2216322 (emergency surgical procedure)
    no history of crohn disease, chronic ulcerative colitis, or familial polyposis
    Descrição

    crohn disease, chronic ulcerative colitis, or familial polyposis

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0010346 (Crohn Disease)
    SNOMED
    34000006
    UMLS CUI [2]
    C0009324 (Ulcerative Colitis)
    SNOMED
    64766004
    UMLS CUI [3]
    C2713443 (Familial Intestinal Polyposis)
    no other malignancy within the past 3 years except for completely resected cervical cancer, skin cancer, or in situ cancer
    Descrição

    comorbidity, malignant neoplasm

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0009488 (Comorbidity)
    UMLS CUI [2]
    C0006826 (Malignant Neoplasms)
    SNOMED
    363346000
    LOINC
    LP100805-3
    prior concurrent therapy:
    Descrição

    concurrent therapy

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0009429 (Combined Modality Therapy)
    SNOMED
    229554006
    see disease characteristics
    Descrição

    see disease characteristics

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0599878 (disease characteristic)
    see patient characteristics
    Descrição

    see patient characteristics

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0815172 (Client Characteristics)
    no concurrent participation in another research protocol
    Descrição

    study participation status

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C2348568 (Study Subject Participation Status)
    participation during follow up allowed
    Descrição

    participation during follow up

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0679823 (Participation)
    UMLS CUI [1,2]
    C1522577 (follow-up)

    Similar models

    Eligibility Colorectal Cancer NCT00625625

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    Alias
    Item Group
    diagnosis of colorectal cancer
    Item
    diagnosis of colorectal cancer as detected by proctosigmoidoscopy, flexible endoscopy, or gastrografin/barium enema
    boolean
    C0011900 (UMLS CUI [1,1])
    C0009402 (UMLS CUI [1,2])
    distant metastases
    Item
    no evidence of distant metastases by ct scan of the abdomen and pelvis and chest x-ray or ct scan of the chest performed within 6 weeks prior to enrollment
    boolean
    C3258247 (UMLS CUI [1])
    preoperative diagnostics
    Item
    preoperative ct scans and testing showing non-specific or non-diagnostic (equivocal) abnormalities may be eligible pending intraoperative exploration
    boolean
    C1318968 (UMLS CUI [1])
    no discovery of distant metastases intra-operatively
    Item
    no discovery of distant metastases intra-operatively
    boolean
    C0027627 (UMLS CUI [1,1])
    C0243164 (UMLS CUI [1,2])
    patient characteristics
    Item
    patient characteristics:
    boolean
    C0815172 (UMLS CUI [1])
    ecog performance status or zubrod performance status
    Item
    ecog performance status (ps) or zubrod ps equal to 2
    boolean
    C1520224 (UMLS CUI [1])
    C3714786 (UMLS CUI [2])
    life expectancy
    Item
    life expectancy > 5 years not including the disease/diagnosis of colorectal cancer
    boolean
    C0023671 (UMLS CUI [1])
    pregnant or nursing
    Item
    not pregnant or nursing
    boolean
    C0032961 (UMLS CUI [1])
    C0006147 (UMLS CUI [2])
    negative pregnancy test
    Item
    negative pregnancy test
    boolean
    C0427780 (UMLS CUI [1])
    contraceptive methods
    Item
    fertile patients must use effective contraception
    boolean
    C0700589 (UMLS CUI [1])
    emergency surgery
    Item
    no requirement for emergent surgery (within 2 hours of presentation) to prevent a life-threatening situation or death including:
    boolean
    C2216322 (UMLS CUI [1])
    perforated colon
    Item
    perforated colon
    boolean
    C0347646 (UMLS CUI [1])
    complete bowel obstruction
    Item
    metabolically significant complete bowel obstruction
    boolean
    C0021843 (UMLS CUI [1,1])
    C0205197 (UMLS CUI [1,2])
    gi bleeding
    Item
    massive gi bleeding
    boolean
    C0017181 (UMLS CUI [1,1])
    C0522501 (UMLS CUI [1,2])
    occult bleeding, partial bowel obstruction, emergency surgery
    Item
    occult bleeding or early or partial bowel obstruction not requiring emergent surgery allowed
    boolean
    C0333282 (UMLS CUI [1])
    C1328480 (UMLS CUI [2])
    C2216322 (UMLS CUI [3])
    crohn disease, chronic ulcerative colitis, or familial polyposis
    Item
    no history of crohn disease, chronic ulcerative colitis, or familial polyposis
    boolean
    C0010346 (UMLS CUI [1])
    C0009324 (UMLS CUI [2])
    C2713443 (UMLS CUI [3])
    comorbidity, malignant neoplasm
    Item
    no other malignancy within the past 3 years except for completely resected cervical cancer, skin cancer, or in situ cancer
    boolean
    C0009488 (UMLS CUI [1])
    C0006826 (UMLS CUI [2])
    concurrent therapy
    Item
    prior concurrent therapy:
    boolean
    C0009429 (UMLS CUI [1])
    see disease characteristics
    Item
    see disease characteristics
    boolean
    C0599878 (UMLS CUI [1])
    see patient characteristics
    Item
    see patient characteristics
    boolean
    C0815172 (UMLS CUI [1])
    study participation status
    Item
    no concurrent participation in another research protocol
    boolean
    C2348568 (UMLS CUI [1])
    participation during follow up
    Item
    participation during follow up allowed
    boolean
    C0679823 (UMLS CUI [1,1])
    C1522577 (UMLS CUI [1,2])

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