ID

16005

Descrição

The Use of Pentoxifylline and Vitamin E in the Treatment of Chronic Breast Pain; ODM derived from: https://clinicaltrials.gov/show/NCT00188669

Link

https://clinicaltrials.gov/show/NCT00188669

Palavras-chave

  1. 05/05/2016 05/05/2016 -
  2. 26/06/2016 26/06/2016 -
Transferido a

26 de junho de 2016

DOI

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Licença

Creative Commons BY 4.0

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    Eligibility Breast Neoplasms NCT00188669

    Eligibility Breast Neoplasms NCT00188669

    Inclusion Criteria
    Descrição

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    uicc tnm stage 0 (i.e. in situ disease), 1 or 2 breast cancer patients treated with conservative surgery and adjuvant radiotherapy with chronic breast pain or tenderness, with or without fibrosis, within 3 months to 3 years following completion of radiotherapy
    Descrição

    breast cancer tnm stage

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0150055
    UMLS CUI [2]
    C0234233
    age 18 to 75 years of age
    Descrição

    age

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    chronic symptoms localised to the breast treated with radiation, i.e. any one or more of the following- pain (not attributable to infection) or tenderness with or without associated oedema, fibrosis, necrosis or ulceration.
    Descrição

    chronic symptoms like pain, tenderness, fibrosis, necrosis or ulceration

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0156323
    breast pain (maximum in the previous 24 hours) measurable on a linear analogue scale with a length of 3cm or greater
    Descrição

    breast pain

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0024902
    prior treatment with radiation to the affected area i.e. in tangential breast fields or boost area
    Descrição

    prior radiation therapy

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C1522449
    radiation completed at least 3 months and no longer than 3 years prior to study entry
    Descrição

    radiation completed

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C1522449
    informed consent
    Descrição

    informed consent

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Descrição

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    active cellulitis in the breast
    Descrição

    Cellulitis of breast

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0392003
    active malignant disease
    Descrição

    Malignant Neoplasms

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0006826
    any medical illness or condition judged likely by the local investigator to preclude safe administration of protocol treatment
    Descrição

    comorbidity not influencing protocol treatment

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0009488
    contraindication to treatment with pentoxifylline (i.e. previously exhibited intolerance to pentoxifylline or other xanthines such as caffeine, theophylline or theobromine; recent cerebral and/or retinal haemorrhage; ischaemic heart disease; hypotension
    Descrição

    contraindication to pentoxifylline

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C1301624
    UMLS CUI [1,2]
    C0030899
    pregnant or lactating women
    Descrição

    pregnant or lactating

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0032961
    UMLS CUI [1,2]
    C0006147

    Similar models

    Eligibility Breast Neoplasms NCT00188669

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    Alias
    Item Group
    C1512693 (UMLS CUI)
    breast cancer tnm stage
    Item
    uicc tnm stage 0 (i.e. in situ disease), 1 or 2 breast cancer patients treated with conservative surgery and adjuvant radiotherapy with chronic breast pain or tenderness, with or without fibrosis, within 3 months to 3 years following completion of radiotherapy
    boolean
    C0150055 (UMLS CUI [1])
    C0234233 (UMLS CUI [2])
    age
    Item
    age 18 to 75 years of age
    boolean
    C0001779 (UMLS CUI [1])
    chronic symptoms like pain, tenderness, fibrosis, necrosis or ulceration
    Item
    chronic symptoms localised to the breast treated with radiation, i.e. any one or more of the following- pain (not attributable to infection) or tenderness with or without associated oedema, fibrosis, necrosis or ulceration.
    boolean
    C0156323 (UMLS CUI [1])
    breast pain
    Item
    breast pain (maximum in the previous 24 hours) measurable on a linear analogue scale with a length of 3cm or greater
    boolean
    C0024902 (UMLS CUI [1])
    prior radiation therapy
    Item
    prior treatment with radiation to the affected area i.e. in tangential breast fields or boost area
    boolean
    C1522449 (UMLS CUI [1])
    radiation completed
    Item
    radiation completed at least 3 months and no longer than 3 years prior to study entry
    boolean
    C0011008 (UMLS CUI [1,1])
    C1522449 (UMLS CUI [1,2])
    informed consent
    Item
    informed consent
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Cellulitis of breast
    Item
    active cellulitis in the breast
    boolean
    C0392003 (UMLS CUI [1])
    Malignant Neoplasms
    Item
    active malignant disease
    boolean
    C0006826 (UMLS CUI [1])
    comorbidity not influencing protocol treatment
    Item
    any medical illness or condition judged likely by the local investigator to preclude safe administration of protocol treatment
    boolean
    C0009488 (UMLS CUI [1])
    contraindication to pentoxifylline
    Item
    contraindication to treatment with pentoxifylline (i.e. previously exhibited intolerance to pentoxifylline or other xanthines such as caffeine, theophylline or theobromine; recent cerebral and/or retinal haemorrhage; ischaemic heart disease; hypotension
    boolean
    C1301624 (UMLS CUI [1,1])
    C0030899 (UMLS CUI [1,2])
    pregnant or lactating
    Item
    pregnant or lactating women
    boolean
    C0032961 (UMLS CUI [1,1])
    C0006147 (UMLS CUI [1,2])

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