ID

30172

Beschrijving

Fludarabine and Alemtuzumab or Cyclophosphamide Followed by Peripheral Blood Stem Cell Transplant or Alemtuzumab in Treating Patients With Advanced or Progressive Chronic Lymphocytic Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00462332

Link

https://clinicaltrials.gov/show/NCT00462332

Trefwoorden

Versies (1)
  1. 16-05-18 16-05-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

16 mei 2018

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 Leukemia NCT00462332

Engels

Eligibility Leukemia NCT00462332

1 Formulieren  
  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00462332
Criteria
Beschrijving

Criteria

diagnosis of chronic lymphocytic leukemia (cll)
Beschrijving

Chronic Lymphocytic Leukemia

Datatype

boolean

Alias
UMLS CUI [1]
C0023434
advanced or progressive disease with ≥ 2 active clinical signs
Beschrijving

Advanced disease | Progressive Disease | Sign or Symptom Quantity

Datatype

boolean

Alias
UMLS CUI [1]
C0679246
UMLS CUI [2]
C1335499
UMLS CUI [3,1]
C3540840
UMLS CUI [3,2]
C1265611
patient characteristics:
Beschrijving

Client Characteristics

Datatype

boolean

Alias
UMLS CUI [1]
C0815172
fertile patients must use adequate contraception
Beschrijving

Fertility Contraceptive methods

Datatype

boolean

Alias
UMLS CUI [1,1]
C0015895
UMLS CUI [1,2]
C0700589
no positive coomb's test with signs of hemolysis
Beschrijving

Exclusion Criteria | Coombs Test Positive | Signs Hemolysis

Datatype

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2,1]
C0009961
UMLS CUI [2,2]
C1514241
UMLS CUI [3,1]
C0311392
UMLS CUI [3,2]
C0019054
no active infection
Beschrijving

Exclusion Communicable Disease

Datatype

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0009450
no uncontrolled severe disease
Beschrijving

Exclusion Disease Severe Uncontrolled

Datatype

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0012634
UMLS CUI [1,3]
C0205082
UMLS CUI [1,4]
C0205318
no known hypersensitivity or anaphylactic reactions to murine antibodies or proteins
Beschrijving

Exclusion Criteria | Hypersensitivity Murine-Derived Monoclonal Antibodies | Anaphylaxis Murine-Derived Monoclonal Antibodies | Hypersensitivity Murine protein | Anaphylaxis Murine protein

Datatype

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C2916903
UMLS CUI [3,1]
C0002792
UMLS CUI [3,2]
C2916903
UMLS CUI [4,1]
C0020517
UMLS CUI [4,2]
C1699668
UMLS CUI [5,1]
C0002792
UMLS CUI [5,2]
C1699668
no other malignancies within the past 2 years except for adequately treated malignancies
Beschrijving

Exclusion Cancer Other | Exception Malignant Neoplasms Treated

Datatype

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C1707251
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0006826
UMLS CUI [2,3]
C1522326
no significant traumatic injury within the past 4 weeks
Beschrijving

Exclusion Traumatic injury

Datatype

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C3263723
no coexisting medical or psychological condition that would limit study compliance
Beschrijving

Exclusion Criteria | Medical condition Limiting Protocol Compliance | Mental condition Limiting Protocol Compliance

Datatype

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C0439801
UMLS CUI [2,3]
C0525058
UMLS CUI [3,1]
C3840291
UMLS CUI [3,2]
C0439801
UMLS CUI [3,3]
C0525058
prior concurrent therapy:
Beschrijving

Therapeutic procedure

Datatype

boolean

Alias
UMLS CUI [1]
C0087111
see disease characteristics
Beschrijving

ID.13

Datatype

boolean

no prior treatment for cll
Beschrijving

Exclusion Prior Therapy Chronic Lymphocytic Leukemia

Datatype

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C0023434
no major surgery within the past 4 weeks
Beschrijving

Exclusion Major surgery

Datatype

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0679637
no prior chemotherapy
Beschrijving

Exclusion Prior Chemotherapy

Datatype

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C1514457
Terug naar het begin van de pagina

Similar models

Eligibility Leukemia NCT00462332

1 Formulieren
  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00462332
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Chronic Lymphocytic Leukemia
Item
diagnosis of chronic lymphocytic leukemia (cll)
boolean
C0023434 (UMLS CUI [1])
Advanced disease | Progressive Disease | Sign or Symptom Quantity
Item
advanced or progressive disease with ≥ 2 active clinical signs
boolean
C0679246 (UMLS CUI [1])
C1335499 (UMLS CUI [2])
C3540840 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Fertility Contraceptive methods
Item
fertile patients must use adequate contraception
boolean
C0015895 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Exclusion Criteria | Coombs Test Positive | Signs Hemolysis
Item
no positive coomb's test with signs of hemolysis
boolean
C0680251 (UMLS CUI [1])
C0009961 (UMLS CUI [2,1])
C1514241 (UMLS CUI [2,2])
C0311392 (UMLS CUI [3,1])
C0019054 (UMLS CUI [3,2])
Exclusion Communicable Disease
Item
no active infection
boolean
C2828389 (UMLS CUI [1,1])
C0009450 (UMLS CUI [1,2])
Exclusion Disease Severe Uncontrolled
Item
no uncontrolled severe disease
boolean
C2828389 (UMLS CUI [1,1])
C0012634 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
C0205318 (UMLS CUI [1,4])
Exclusion Criteria | Hypersensitivity Murine-Derived Monoclonal Antibodies | Anaphylaxis Murine-Derived Monoclonal Antibodies | Hypersensitivity Murine protein | Anaphylaxis Murine protein
Item
no known hypersensitivity or anaphylactic reactions to murine antibodies or proteins
boolean
C0680251 (UMLS CUI [1])
C0020517 (UMLS CUI [2,1])
C2916903 (UMLS CUI [2,2])
C0002792 (UMLS CUI [3,1])
C2916903 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C1699668 (UMLS CUI [4,2])
C0002792 (UMLS CUI [5,1])
C1699668 (UMLS CUI [5,2])
Exclusion Cancer Other | Exception Malignant Neoplasms Treated
Item
no other malignancies within the past 2 years except for adequately treated malignancies
boolean
C2828389 (UMLS CUI [1,1])
C1707251 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0006826 (UMLS CUI [2,2])
C1522326 (UMLS CUI [2,3])
Exclusion Traumatic injury
Item
no significant traumatic injury within the past 4 weeks
boolean
C2828389 (UMLS CUI [1,1])
C3263723 (UMLS CUI [1,2])
Exclusion Criteria | Medical condition Limiting Protocol Compliance | Mental condition Limiting Protocol Compliance
Item
no coexisting medical or psychological condition that would limit study compliance
boolean
C0680251 (UMLS CUI [1])
C3843040 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0525058 (UMLS CUI [2,3])
C3840291 (UMLS CUI [3,1])
C0439801 (UMLS CUI [3,2])
C0525058 (UMLS CUI [3,3])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
ID.13
Item
see disease characteristics
boolean
Exclusion Prior Therapy Chronic Lymphocytic Leukemia
Item
no prior treatment for cll
boolean
C2828389 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C0023434 (UMLS CUI [1,3])
Exclusion Major surgery
Item
no major surgery within the past 4 weeks
boolean
C2828389 (UMLS CUI [1,1])
C0679637 (UMLS CUI [1,2])
Exclusion Prior Chemotherapy
Item
no prior chemotherapy
boolean
C2828389 (UMLS CUI [1,1])
C1514457 (UMLS CUI [1,2])
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