ID

24579

Descrizione

Positron Emission Tomography (PET)-Scan in the Evaluation of High Tumor Burden Follicular Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00915096

collegamento

https://clinicaltrials.gov/show/NCT00915096

Keywords

versioni (1)
  1. 07/08/17 07/08/17 -
Caricato su

7 agosto 2017

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
Commenti del modello :

Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.

Torna ai commenti del modello
Commenti del gruppo di articoli per :

Commenti dell'articolo per :

Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.

Eligibility Lymphoma, Follicular NCT00915096

Inglese

Eligibility Lymphoma, Follicular NCT00915096

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with malignant non-hodgkin follicular lymphoma (histologic grade 1 to 3 in the who classification), histologically confirmed,
Descrizione

Follicular Lymphoma WHO tumor classification

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0024301
UMLS CUI [1,2]
C1301142
patients who have not previously been treated for this disease,
Descrizione

Disease untreated

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0332155
introducing one of the criteria for high tumor burden,
Descrizione

Criteria Tumor Burden High

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1449699
UMLS CUI [1,3]
C0205250
patients aged over 18 and under 80 years,
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
patients whose ecog condition is ≤ 2,
Descrizione

ECOG performance status

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1520224
patients whose haematological functions are adequate within 28 days preceding the treatment (hemoglobin ≥8,0g/dl; neutrophils ≥1,5e-9/l, platelets ≥100e-9/l),
Descrizione

Hematologic function | Hemoglobin measurement | Neutrophil count | Platelet Count measurement

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0221130
UMLS CUI [2]
C0518015
UMLS CUI [3]
C0200633
UMLS CUI [4]
C0032181
patient had the pet examination less than a month before the start of chemotherapy.
Descrizione

Positron-Emission Tomography

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032743
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with lymphoma who have already transformed or been treated for this disease,
Descrizione

Lymphoma Transformed | Lymphoma Treated

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0024299
UMLS CUI [1,2]
C0457344
UMLS CUI [2,1]
C0024299
UMLS CUI [2,2]
C1522326
patients whose lymphoma is stage 3b,
Descrizione

Lymphoma WHO tumor classification

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0024299
UMLS CUI [1,2]
C1301142
patients with impaired central nervous system,
Descrizione

Central Nervous System Impaired

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C3714787
UMLS CUI [1,2]
C0221099
patients regularly taking corticosteroids during the 4 weeks preceding the treatment (unless the dose administered is equivalent to ≤20 mg/day prednisone).
Descrizione

Adrenal Cortex Hormones Regular | Exception Dose Equivalent Prednisone U/day

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0001617
UMLS CUI [1,2]
C0205272
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0178602
UMLS CUI [2,3]
C0205163
UMLS CUI [2,4]
C0032952
UMLS CUI [2,5]
C0456683
patients who have undergone major surgery during the 28 days preceding the inclusion,
Descrizione

major surgery

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0679637
patients with low kidney and/or liver function,
Descrizione

Decreased renal function | Decreased liver function

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0232807
UMLS CUI [2]
C0232744
patients with hiv + or had an infection with hbv or hcv less than 4 weeks. patients with hepatitis b serology is positive unless the sign is related to vaccination,
Descrizione

HIV Seropositivity | Hepatitis B | Hepatitis C | HEPATITIS B SEROLOGY POSITIVE | Exception Sign Due to Vaccination

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0019699
UMLS CUI [2]
C0019163
UMLS CUI [3]
C0019196
UMLS CUI [4]
C0744838
UMLS CUI [5,1]
C1705847
UMLS CUI [5,2]
C0311392
UMLS CUI [5,3]
C0678226
UMLS CUI [5,4]
C0042196
patients whose life expectancy ≤ 6 months,
Descrizione

Life Expectancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0023671
patients sensitive or allergic to murine products,
Descrizione

Hypersensitivity Product Murine

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1514468
UMLS CUI [1,3]
C0026809
patients who participated in another clinical trial during the 30 days preceding the recording,
Descrizione

Study Subject Participation Status

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2348568
patients with other medical problems or psychological succeptibles interfere with the study,
Descrizione

Patient Problem Interferes with Clinical Trial | Mental problem Interferes with Clinical Trial

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1254481
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0008976
UMLS CUI [2,1]
C0848067
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0008976
patients under adult supervision.
Descrizione

Patient Supervision Adult

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0038842
UMLS CUI [1,3]
C0001675
Ritorna all'inizio della pagina

Similar models

Eligibility Lymphoma, Follicular NCT00915096

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Follicular Lymphoma WHO tumor classification
Item
patients with malignant non-hodgkin follicular lymphoma (histologic grade 1 to 3 in the who classification), histologically confirmed,
boolean
C0024301 (UMLS CUI [1,1])
C1301142 (UMLS CUI [1,2])
Disease untreated
Item
patients who have not previously been treated for this disease,
boolean
C0012634 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
Criteria Tumor Burden High
Item
introducing one of the criteria for high tumor burden,
boolean
C0243161 (UMLS CUI [1,1])
C1449699 (UMLS CUI [1,2])
C0205250 (UMLS CUI [1,3])
Age
Item
patients aged over 18 and under 80 years,
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
patients whose ecog condition is ≤ 2,
boolean
C1520224 (UMLS CUI [1])
Hematologic function | Hemoglobin measurement | Neutrophil count | Platelet Count measurement
Item
patients whose haematological functions are adequate within 28 days preceding the treatment (hemoglobin ≥8,0g/dl; neutrophils ≥1,5e-9/l, platelets ≥100e-9/l),
boolean
C0221130 (UMLS CUI [1])
C0518015 (UMLS CUI [2])
C0200633 (UMLS CUI [3])
C0032181 (UMLS CUI [4])
Positron-Emission Tomography
Item
patient had the pet examination less than a month before the start of chemotherapy.
boolean
C0032743 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Lymphoma Transformed | Lymphoma Treated
Item
patients with lymphoma who have already transformed or been treated for this disease,
boolean
C0024299 (UMLS CUI [1,1])
C0457344 (UMLS CUI [1,2])
C0024299 (UMLS CUI [2,1])
C1522326 (UMLS CUI [2,2])
Lymphoma WHO tumor classification
Item
patients whose lymphoma is stage 3b,
boolean
C0024299 (UMLS CUI [1,1])
C1301142 (UMLS CUI [1,2])
Central Nervous System Impaired
Item
patients with impaired central nervous system,
boolean
C3714787 (UMLS CUI [1,1])
C0221099 (UMLS CUI [1,2])
Adrenal Cortex Hormones Regular | Exception Dose Equivalent Prednisone U/day
Item
patients regularly taking corticosteroids during the 4 weeks preceding the treatment (unless the dose administered is equivalent to ≤20 mg/day prednisone).
boolean
C0001617 (UMLS CUI [1,1])
C0205272 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0205163 (UMLS CUI [2,3])
C0032952 (UMLS CUI [2,4])
C0456683 (UMLS CUI [2,5])
major surgery
Item
patients who have undergone major surgery during the 28 days preceding the inclusion,
boolean
C0679637 (UMLS CUI [1])
Decreased renal function | Decreased liver function
Item
patients with low kidney and/or liver function,
boolean
C0232807 (UMLS CUI [1])
C0232744 (UMLS CUI [2])
HIV Seropositivity | Hepatitis B | Hepatitis C | HEPATITIS B SEROLOGY POSITIVE | Exception Sign Due to Vaccination
Item
patients with hiv + or had an infection with hbv or hcv less than 4 weeks. patients with hepatitis b serology is positive unless the sign is related to vaccination,
boolean
C0019699 (UMLS CUI [1])
C0019163 (UMLS CUI [2])
C0019196 (UMLS CUI [3])
C0744838 (UMLS CUI [4])
C1705847 (UMLS CUI [5,1])
C0311392 (UMLS CUI [5,2])
C0678226 (UMLS CUI [5,3])
C0042196 (UMLS CUI [5,4])
Life Expectancy
Item
patients whose life expectancy ≤ 6 months,
boolean
C0023671 (UMLS CUI [1])
Hypersensitivity Product Murine
Item
patients sensitive or allergic to murine products,
boolean
C0020517 (UMLS CUI [1,1])
C1514468 (UMLS CUI [1,2])
C0026809 (UMLS CUI [1,3])
Study Subject Participation Status
Item
patients who participated in another clinical trial during the 30 days preceding the recording,
boolean
C2348568 (UMLS CUI [1])
Patient Problem Interferes with Clinical Trial | Mental problem Interferes with Clinical Trial
Item
patients with other medical problems or psychological succeptibles interfere with the study,
boolean
C1254481 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0848067 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
Patient Supervision Adult
Item
patients under adult supervision.
boolean
C0030705 (UMLS CUI [1,1])
C0038842 (UMLS CUI [1,2])
C0001675 (UMLS CUI [1,3])
Ritorna all'inizio della pagina 

Contatto

Si prega di utilizzare questo modulo per feedback, domande e suggerimenti per miglioramenti.

I campi contrassegnati da * sono obbligatori.

Aiuto

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