ID

15398

Beschreibung

Effects of Anticoagulant Preventive Injection in Patients With Blood Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02260414

Link

https://clinicaltrials.gov/show/NCT02260414

Stichworte

Versionen (1)
  1. 30.05.16 30.05.16 -
Hochgeladen am

30. Mai 2016

DOI

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Creative Commons BY 4.0
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Eligibility Lymphoma NCT02260414

Englisch

Eligibility Lymphoma NCT02260414

1 Formulare  
  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT02260414
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. body weight between 40 and 100 kg
Beschreibung

Body Weight

Datentyp

boolean

Alias
UMLS CUI [1]
C0005910
2. patient:
Beschreibung

Patient

Datentyp

boolean

Alias
UMLS CUI [1]
C0030705
2a- with multiple myeloma indication with de novo standard treatment thalidomide or lenalidomide or erythropoietin (group 1) 2b- or hospitalized for aggressive lymphoma treated with chemotherapy (group 2) 2c- or older than 40 years and hospitalized at least three days for an acute medical pathology type of acute respiratory or cardiac (group 3) decompensation
Beschreibung

Lymphoma stage | Indication Multiple Myeloma | Therapeutic procedure Thalidomide | Therapeutic procedure lenalidomide | Therapeutic procedure Erythropoietin | Hospitalization | Aggressive Non-Hodgkin Lymphoma | Chemotherapy Regimen | Age | Acute respiratory decompensation | Heart Decompensation

Datentyp

boolean

Alias
UMLS CUI [1]
C1272836
UMLS CUI [2,1]
C3146298
UMLS CUI [2,2]
C0026764
UMLS CUI [3,1]
C0087111
UMLS CUI [3,2]
C0039736
UMLS CUI [4,1]
C0087111
UMLS CUI [4,2]
C1144149
UMLS CUI [5,1]
C0087111
UMLS CUI [5,2]
C0014822
UMLS CUI [6]
C0019993
UMLS CUI [7]
C1332225
UMLS CUI [8]
C0392920
UMLS CUI [9]
C0001779
UMLS CUI [10]
C0748352
UMLS CUI [11]
C1961112
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient requiring anticoagulant therapy at curative doses
Beschreibung

Anticoagulant therapy Curative

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0150457
UMLS CUI [1,2]
C1880198
patients with a lower platelet count 80 g / l
Beschreibung

Decreased platelet count

Datentyp

boolean

Alias
UMLS CUI [1]
C0392386
subject with a history of heparin-induced thrombocytopenia
Beschreibung

Heparin-induced thrombocytopenia

Datentyp

boolean

Alias
UMLS CUI [1]
C0272285
subject with a history of hemorrhagic disease
Beschreibung

Hemorrhagic Disorders

Datentyp

boolean

Alias
UMLS CUI [1]
C0019087
history of severe trauma within 6 weeks prior to enrollment
Beschreibung

Trauma Severe

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3714660
UMLS CUI [1,2]
C0205082
organic lesion at risk of bleeding
Beschreibung

Lesion Organ

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0178784
poor renal with creatinine clearance <30 ml / min
Beschreibung

Abnormal renal function | Creatinine clearance measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0151746
UMLS CUI [2]
C0373595
hypersensitivity to tinzaparin
Beschreibung

Hypersensitivity tinzaparin

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0216278
events or bleeding tendencies associated with coagulation disorders
Beschreibung

Event Associated with Blood Coagulation Disorders | Bleeding tendency Associated with Blood Coagulation Disorders

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0441471
UMLS CUI [1,2]
C0332281
UMLS CUI [1,3]
C0005779
UMLS CUI [2,1]
C1458140
UMLS CUI [2,2]
C0332281
UMLS CUI [2,3]
C0005779
subject on oral anticoagulant
Beschreibung

oral anticoagulants

Datentyp

boolean

Alias
UMLS CUI [1]
C0354604
for group 3: presence of hematological malignancy or active cancer
Beschreibung

Hematologic Neoplasms | Malignant Neoplasms

Datentyp

boolean

Alias
UMLS CUI [1]
C0376545
UMLS CUI [2]
C0006826
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Ähnliche Modelle

Eligibility Lymphoma NCT02260414

1 Formulare
  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT02260414
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Body Weight
Item
1. body weight between 40 and 100 kg
boolean
C0005910 (UMLS CUI [1])
Patient
Item
2. patient:
boolean
C0030705 (UMLS CUI [1])
Lymphoma stage | Indication Multiple Myeloma | Therapeutic procedure Thalidomide | Therapeutic procedure lenalidomide | Therapeutic procedure Erythropoietin | Hospitalization | Aggressive Non-Hodgkin Lymphoma | Chemotherapy Regimen | Age | Acute respiratory decompensation | Heart Decompensation
Item
2a- with multiple myeloma indication with de novo standard treatment thalidomide or lenalidomide or erythropoietin (group 1) 2b- or hospitalized for aggressive lymphoma treated with chemotherapy (group 2) 2c- or older than 40 years and hospitalized at least three days for an acute medical pathology type of acute respiratory or cardiac (group 3) decompensation
boolean
C1272836 (UMLS CUI [1])
C3146298 (UMLS CUI [2,1])
C0026764 (UMLS CUI [2,2])
C0087111 (UMLS CUI [3,1])
C0039736 (UMLS CUI [3,2])
C0087111 (UMLS CUI [4,1])
C1144149 (UMLS CUI [4,2])
C0087111 (UMLS CUI [5,1])
C0014822 (UMLS CUI [5,2])
C0019993 (UMLS CUI [6])
C1332225 (UMLS CUI [7])
C0392920 (UMLS CUI [8])
C0001779 (UMLS CUI [9])
C0748352 (UMLS CUI [10])
C1961112 (UMLS CUI [11])
Item Group
C0680251 (UMLS CUI)
Anticoagulant therapy Curative
Item
patient requiring anticoagulant therapy at curative doses
boolean
C0150457 (UMLS CUI [1,1])
C1880198 (UMLS CUI [1,2])
Decreased platelet count
Item
patients with a lower platelet count 80 g / l
boolean
C0392386 (UMLS CUI [1])
Heparin-induced thrombocytopenia
Item
subject with a history of heparin-induced thrombocytopenia
boolean
C0272285 (UMLS CUI [1])
Hemorrhagic Disorders
Item
subject with a history of hemorrhagic disease
boolean
C0019087 (UMLS CUI [1])
Trauma Severe
Item
history of severe trauma within 6 weeks prior to enrollment
boolean
C3714660 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Lesion Organ
Item
organic lesion at risk of bleeding
boolean
C0221198 (UMLS CUI [1,1])
C0178784 (UMLS CUI [1,2])
Abnormal renal function | Creatinine clearance measurement
Item
poor renal with creatinine clearance <30 ml / min
boolean
C0151746 (UMLS CUI [1])
C0373595 (UMLS CUI [2])
Hypersensitivity tinzaparin
Item
hypersensitivity to tinzaparin
boolean
C0020517 (UMLS CUI [1,1])
C0216278 (UMLS CUI [1,2])
Event Associated with Blood Coagulation Disorders | Bleeding tendency Associated with Blood Coagulation Disorders
Item
events or bleeding tendencies associated with coagulation disorders
boolean
C0441471 (UMLS CUI [1,1])
C0332281 (UMLS CUI [1,2])
C0005779 (UMLS CUI [1,3])
C1458140 (UMLS CUI [2,1])
C0332281 (UMLS CUI [2,2])
C0005779 (UMLS CUI [2,3])
oral anticoagulants
Item
subject on oral anticoagulant
boolean
C0354604 (UMLS CUI [1])
Hematologic Neoplasms | Malignant Neoplasms
Item
for group 3: presence of hematological malignancy or active cancer
boolean
C0376545 (UMLS CUI [1])
C0006826 (UMLS CUI [2])
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