ID

18028

Beschreibung

Mobilization of Stem Cells With Plerixafor, Chemotherapy and G-CSF in Multiple Myeloma or Non-Hodgkin's Lymphoma Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00322387

Link

https://clinicaltrials.gov/show/NCT00322387

Stichworte

Versionen (1)
  1. 15.10.16 15.10.16 -
Hochgeladen am

15. Oktober 2016

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Lymphoma, Non-Hodgkin NCT00322387

Englisch

Eligibility Lymphoma, Non-Hodgkin NCT00322387

1 Formulare  
Criteria
Beschreibung

Criteria

mm in first partial response/complete response, first relapse, or second partial/complete response
Beschreibung

Multiple Myeloma partial response First | Multiple Myeloma complete response First | Multiple Myeloma First Relapse | Multiple Myeloma partial response second | Multiple Myeloma complete response second

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0026764
UMLS CUI [1,2]
C1521726
UMLS CUI [1,3]
C0205435
UMLS CUI [2,1]
C0026764
UMLS CUI [2,2]
C0677874
UMLS CUI [2,3]
C0205435
UMLS CUI [3,1]
C0026764
UMLS CUI [3,2]
C4054953
UMLS CUI [4,1]
C0026764
UMLS CUI [4,2]
C1521726
UMLS CUI [4,3]
C0205436
UMLS CUI [5,1]
C0026764
UMLS CUI [5,2]
C0677874
UMLS CUI [5,3]
C0205436
nhl in first or second partial or complete remission
Beschreibung

Non-Hodgkin Lymphoma partial response First | Non-Hodgkin Lymphoma partial response second | Non-Hodgkin Lymphoma complete remission First | Non-Hodgkin Lymphoma complete remission second

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0024305
UMLS CUI [1,2]
C1521726
UMLS CUI [1,3]
C0205435
UMLS CUI [2,1]
C0024305
UMLS CUI [2,2]
C1521726
UMLS CUI [2,3]
C0205436
UMLS CUI [3,1]
C0024305
UMLS CUI [3,2]
C0677874
UMLS CUI [3,3]
C0205435
UMLS CUI [4,1]
C0024305
UMLS CUI [4,2]
C0677874
UMLS CUI [4,3]
C0205436
nhl patients who do not have bone marrow involvement and < 10% for follicular involvement
Beschreibung

Lymphoma, Non-Hodgkin | Bone Marrow Involvement | Involvement Follicular Percentage

Datentyp

boolean

Alias
UMLS CUI [1]
C0024305
UMLS CUI [2,1]
C0005953
UMLS CUI [2,2]
C1314939
UMLS CUI [3,1]
C1314939
UMLS CUI [3,2]
C0439682
UMLS CUI [3,3]
C0439165
mm patients who have stable disease with < 40% bone marrow involvement
Beschreibung

Multiple Myeloma Stable | Bone Marrow Percentage Involvement

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0026764
UMLS CUI [1,2]
C0205360
UMLS CUI [2,1]
C0005953
UMLS CUI [2,2]
C0439165
UMLS CUI [2,3]
C1314939
no more than three prior regimens of chemotherapy (thalidomide and decadron are not considered chemotherapy)
Beschreibung

Prior Chemotherapy Quantity | Thalidomide | Decadron

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C1265611
UMLS CUI [2]
C0039736
UMLS CUI [3]
C0740057
eastern cooperative oncology group (ecog) performance status of 0 or 1
Beschreibung

ECOG performance status

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
white blood cell count (wbc) >3.0 x 10^9/l
Beschreibung

White Blood Cell Count procedure

Datentyp

boolean

Alias
UMLS CUI [1]
C0023508
absolute neutrophil count >1.5 x 10^9/l
Beschreibung

Absolute neutrophil count

Datentyp

boolean

Alias
UMLS CUI [1]
C0948762
platelet count >100 x 10^9/l
Beschreibung

Platelet Count measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0032181
exclusion criteria (abbreviated list):
Beschreibung

Exclusion Criteria

Datentyp

boolean

Alias
UMLS CUI [1]
C0680251
brain metastases or carcinomatous meningitis
Beschreibung

Metastatic malignant neoplasm to brain | Meningeal Carcinomatosis

Datentyp

boolean

Alias
UMLS CUI [1]
C0220650
UMLS CUI [2]
C0220654
hypercalcaemia [>1 mg/dl above the upper limit of normal (uln)]
Beschreibung

Hypercalcemia

Datentyp

boolean

Alias
UMLS CUI [1]
C0020437
cardiovascular disease that includes proven or predisposition to ventricular arrhythmias
Beschreibung

Cardiovascular Diseases | Ventricular arrhythmia | Ventricular arrhythmia Predisposition

Datentyp

boolean

Alias
UMLS CUI [1]
C0007222
UMLS CUI [2]
C0085612
UMLS CUI [3,1]
C0085612
UMLS CUI [3,2]
C0220898
acute infection
Beschreibung

Communicable Disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0009450
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Ähnliche Modelle

Eligibility Lymphoma, Non-Hodgkin NCT00322387

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Multiple Myeloma partial response First | Multiple Myeloma complete response First | Multiple Myeloma First Relapse | Multiple Myeloma partial response second | Multiple Myeloma complete response second
Item
mm in first partial response/complete response, first relapse, or second partial/complete response
boolean
C0026764 (UMLS CUI [1,1])
C1521726 (UMLS CUI [1,2])
C0205435 (UMLS CUI [1,3])
C0026764 (UMLS CUI [2,1])
C0677874 (UMLS CUI [2,2])
C0205435 (UMLS CUI [2,3])
C0026764 (UMLS CUI [3,1])
C4054953 (UMLS CUI [3,2])
C0026764 (UMLS CUI [4,1])
C1521726 (UMLS CUI [4,2])
C0205436 (UMLS CUI [4,3])
C0026764 (UMLS CUI [5,1])
C0677874 (UMLS CUI [5,2])
C0205436 (UMLS CUI [5,3])
Non-Hodgkin Lymphoma partial response First | Non-Hodgkin Lymphoma partial response second | Non-Hodgkin Lymphoma complete remission First | Non-Hodgkin Lymphoma complete remission second
Item
nhl in first or second partial or complete remission
boolean
C0024305 (UMLS CUI [1,1])
C1521726 (UMLS CUI [1,2])
C0205435 (UMLS CUI [1,3])
C0024305 (UMLS CUI [2,1])
C1521726 (UMLS CUI [2,2])
C0205436 (UMLS CUI [2,3])
C0024305 (UMLS CUI [3,1])
C0677874 (UMLS CUI [3,2])
C0205435 (UMLS CUI [3,3])
C0024305 (UMLS CUI [4,1])
C0677874 (UMLS CUI [4,2])
C0205436 (UMLS CUI [4,3])
Lymphoma, Non-Hodgkin | Bone Marrow Involvement | Involvement Follicular Percentage
Item
nhl patients who do not have bone marrow involvement and < 10% for follicular involvement
boolean
C0024305 (UMLS CUI [1])
C0005953 (UMLS CUI [2,1])
C1314939 (UMLS CUI [2,2])
C1314939 (UMLS CUI [3,1])
C0439682 (UMLS CUI [3,2])
C0439165 (UMLS CUI [3,3])
Multiple Myeloma Stable | Bone Marrow Percentage Involvement
Item
mm patients who have stable disease with < 40% bone marrow involvement
boolean
C0026764 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0005953 (UMLS CUI [2,1])
C0439165 (UMLS CUI [2,2])
C1314939 (UMLS CUI [2,3])
Prior Chemotherapy Quantity | Thalidomide | Decadron
Item
no more than three prior regimens of chemotherapy (thalidomide and decadron are not considered chemotherapy)
boolean
C1514457 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0039736 (UMLS CUI [2])
C0740057 (UMLS CUI [3])
ECOG performance status
Item
eastern cooperative oncology group (ecog) performance status of 0 or 1
boolean
C1520224 (UMLS CUI [1])
White Blood Cell Count procedure
Item
white blood cell count (wbc) >3.0 x 10^9/l
boolean
C0023508 (UMLS CUI [1])
Absolute neutrophil count
Item
absolute neutrophil count >1.5 x 10^9/l
boolean
C0948762 (UMLS CUI [1])
Platelet Count measurement
Item
platelet count >100 x 10^9/l
boolean
C0032181 (UMLS CUI [1])
Exclusion Criteria
Item
exclusion criteria (abbreviated list):
boolean
C0680251 (UMLS CUI [1])
Metastatic malignant neoplasm to brain | Meningeal Carcinomatosis
Item
brain metastases or carcinomatous meningitis
boolean
C0220650 (UMLS CUI [1])
C0220654 (UMLS CUI [2])
Hypercalcemia
Item
hypercalcaemia [>1 mg/dl above the upper limit of normal (uln)]
boolean
C0020437 (UMLS CUI [1])
Cardiovascular Diseases | Ventricular arrhythmia | Ventricular arrhythmia Predisposition
Item
cardiovascular disease that includes proven or predisposition to ventricular arrhythmias
boolean
C0007222 (UMLS CUI [1])
C0085612 (UMLS CUI [2])
C0085612 (UMLS CUI [3,1])
C0220898 (UMLS CUI [3,2])
Communicable Disease
Item
acute infection
boolean
C0009450 (UMLS CUI [1])
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