ID

44023

Beschreibung

"REDUCE" - A Clinical Research Study To Reduce The Incidence Of Prostate Cancer In Men Who Are At Increased Risk; ODM derived from: https://clinicaltrials.gov/show/NCT00056407

Link

https://clinicaltrials.gov/show/NCT00056407

Stichworte

  1. 02.11.16 02.11.16 -
  2. 20.09.21 20.09.21 -
Hochgeladen am

20. September 2021

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0

Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Itemgroup Kommentare für :

Item Kommentare für :


    Keine Kommentare

    Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

    Eligibility Neoplasms, Prostate DRKS00009657 NCT00056407

    Eligibility Neoplasms, Prostate NCT00056407

    Inclusion Criteria
    Beschreibung

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    informed consent to participate in study.
    Beschreibung

    Informed Consent

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    have had a single negative prostate biopsy within 6 months prior to enrollment in study.
    Beschreibung

    Biopsy of prostate Negative Single

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0194804
    UMLS CUI [1,2]
    C1513916
    UMLS CUI [1,3]
    C0205171
    have a psa (prostate specific antigen) between 2.5 and 10 if 50-60 years of age; or a psa between 3.0 and 10 if over age 60.
    Beschreibung

    Prostate-Specific Antigen | Age

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0138741
    UMLS CUI [2]
    C0001779
    ability and will to participate in study for 4 years.
    Beschreibung

    Study Subject Participation Status Duration

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C2348568
    UMLS CUI [1,2]
    C0449238
    Exclusion Criteria
    Beschreibung

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    more than one previous negative prostate biopsy.
    Beschreibung

    Biopsy of prostate Negative Quantity

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0194804
    UMLS CUI [1,2]
    C1513916
    UMLS CUI [1,3]
    C1265611
    history of prostate cancer.
    Beschreibung

    Prostate carcinoma

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0600139
    previous prostate surgery.
    Beschreibung

    Operation on prostate

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0194790
    inability to urinate requiring the need of a catheter during the previous 2 years.
    Beschreibung

    Unable to urinate | Catheter Patient need for

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0849752
    UMLS CUI [2,1]
    C0085590
    UMLS CUI [2,2]
    C0686904
    any condition (other than benign prostatic hypertrophy) which may result in urinary symptoms or changes in urine flow rate.
    Beschreibung

    Condition Resulting in Urinary symptoms | Condition Resulting in Urine Flow Rate Change | Benign prostatic hypertrophy

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0348080
    UMLS CUI [1,2]
    C0332294
    UMLS CUI [1,3]
    C0426359
    UMLS CUI [2,1]
    C0348080
    UMLS CUI [2,2]
    C0332294
    UMLS CUI [2,3]
    C0042036
    UMLS CUI [2,4]
    C2826285
    UMLS CUI [2,5]
    C0392747
    UMLS CUI [3]
    C1704272
    cancer within previous 5 years (other than basal or squamous cell cancers of the skin).
    Beschreibung

    Malignant Neoplasms | Basal cell carcinoma | Squamous cell carcinoma of skin

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0006826
    UMLS CUI [2]
    C0007117
    UMLS CUI [3]
    C0553723
    any unstable serious medical condition.
    Beschreibung

    Medical condition Serious Unstable

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C3843040
    UMLS CUI [1,2]
    C0205404
    UMLS CUI [1,3]
    C0443343
    use within the past 12 months of finasteride (proscar or propecia), dutasteride (avodart), testosterone, or drugs that can block the action of male hormones.
    Beschreibung

    Finasteride | Proscar | Propecia | Dutasteride | Avodart | Testosterone | Androgen Antagonists

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0060389
    UMLS CUI [2]
    C0678149
    UMLS CUI [3]
    C0722858
    UMLS CUI [4]
    C0754659
    UMLS CUI [5]
    C1170079
    UMLS CUI [6]
    C0039601
    UMLS CUI [7]
    C0002842

    Ähnliche Modelle

    Eligibility Neoplasms, Prostate NCT00056407

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Informed Consent
    Item
    informed consent to participate in study.
    boolean
    C0021430 (UMLS CUI [1])
    Biopsy of prostate Negative Single
    Item
    have had a single negative prostate biopsy within 6 months prior to enrollment in study.
    boolean
    C0194804 (UMLS CUI [1,1])
    C1513916 (UMLS CUI [1,2])
    C0205171 (UMLS CUI [1,3])
    Prostate-Specific Antigen | Age
    Item
    have a psa (prostate specific antigen) between 2.5 and 10 if 50-60 years of age; or a psa between 3.0 and 10 if over age 60.
    boolean
    C0138741 (UMLS CUI [1])
    C0001779 (UMLS CUI [2])
    Study Subject Participation Status Duration
    Item
    ability and will to participate in study for 4 years.
    boolean
    C2348568 (UMLS CUI [1,1])
    C0449238 (UMLS CUI [1,2])
    Item Group
    C0680251 (UMLS CUI)
    Biopsy of prostate Negative Quantity
    Item
    more than one previous negative prostate biopsy.
    boolean
    C0194804 (UMLS CUI [1,1])
    C1513916 (UMLS CUI [1,2])
    C1265611 (UMLS CUI [1,3])
    Prostate carcinoma
    Item
    history of prostate cancer.
    boolean
    C0600139 (UMLS CUI [1])
    Operation on prostate
    Item
    previous prostate surgery.
    boolean
    C0194790 (UMLS CUI [1])
    Unable to urinate | Catheter Patient need for
    Item
    inability to urinate requiring the need of a catheter during the previous 2 years.
    boolean
    C0849752 (UMLS CUI [1])
    C0085590 (UMLS CUI [2,1])
    C0686904 (UMLS CUI [2,2])
    Condition Resulting in Urinary symptoms | Condition Resulting in Urine Flow Rate Change | Benign prostatic hypertrophy
    Item
    any condition (other than benign prostatic hypertrophy) which may result in urinary symptoms or changes in urine flow rate.
    boolean
    C0348080 (UMLS CUI [1,1])
    C0332294 (UMLS CUI [1,2])
    C0426359 (UMLS CUI [1,3])
    C0348080 (UMLS CUI [2,1])
    C0332294 (UMLS CUI [2,2])
    C0042036 (UMLS CUI [2,3])
    C2826285 (UMLS CUI [2,4])
    C0392747 (UMLS CUI [2,5])
    C1704272 (UMLS CUI [3])
    Malignant Neoplasms | Basal cell carcinoma | Squamous cell carcinoma of skin
    Item
    cancer within previous 5 years (other than basal or squamous cell cancers of the skin).
    boolean
    C0006826 (UMLS CUI [1])
    C0007117 (UMLS CUI [2])
    C0553723 (UMLS CUI [3])
    Medical condition Serious Unstable
    Item
    any unstable serious medical condition.
    boolean
    C3843040 (UMLS CUI [1,1])
    C0205404 (UMLS CUI [1,2])
    C0443343 (UMLS CUI [1,3])
    Finasteride | Proscar | Propecia | Dutasteride | Avodart | Testosterone | Androgen Antagonists
    Item
    use within the past 12 months of finasteride (proscar or propecia), dutasteride (avodart), testosterone, or drugs that can block the action of male hormones.
    boolean
    C0060389 (UMLS CUI [1])
    C0678149 (UMLS CUI [2])
    C0722858 (UMLS CUI [3])
    C0754659 (UMLS CUI [4])
    C1170079 (UMLS CUI [5])
    C0039601 (UMLS CUI [6])
    C0002842 (UMLS CUI [7])

    Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

    Zum Video