ID

30393

Beschrijving

Stem Cell Mobilization With Pegfilgrastim in Lymphoma and Myeloma; ODM derived from: https://clinicaltrials.gov/show/NCT00794261

Link

https://clinicaltrials.gov/show/NCT00794261

Trefwoorden

Versies (2)
  1. 01-06-18 01-06-18 -
  2. 01-06-18 01-06-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

1 juni 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 Lymphoma NCT00794261

Engels

Eligibility Lymphoma NCT00794261

1 Formulieren  
  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00794261
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female patients aged ≥ 18 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
patients with histologically confirmed lymphoma or myeloma
Beschrijving

Lymphoma | Multiple Myeloma

Datatype

boolean

Alias
UMLS CUI [1]
C0024299
UMLS CUI [2]
C0026764
treatment with high-dose chemotherapy before inclusion
Beschrijving

High-dose chemotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C1328050
intensification with high dose melphalan for patients with myeloma
Beschrijving

Melphalan High dose | Multiple Myeloma

Datatype

boolean

Alias
UMLS CUI [1,1]
C0025241
UMLS CUI [1,2]
C0444956
UMLS CUI [2]
C0026764
whatever the conditioning regimen, except tbi for patients with 1st relapse of hodgkin's lymphoma or with mnhl nb: patients having received two intensification courses are eligible if there has been more than 100 days between courses.
Beschrijving

Transplantation Conditioning | Exception Whole-Body Irradiation First Relapse Hodgkin Disease | Other Coding | Consolidation therapy Quantity

Datatype

boolean

Alias
UMLS CUI [1]
C0376450
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0043162
UMLS CUI [2,3]
C4054953
UMLS CUI [2,4]
C0019829
UMLS CUI [3]
C3846158
UMLS CUI [4,1]
C1511484
UMLS CUI [4,2]
C1265611
autologous psc transplantation at the time of inclusion
Beschrijving

Primary sclerosing cholangitis Autologous Transplantation

Datatype

boolean

Alias
UMLS CUI [1,1]
C0566602
UMLS CUI [1,2]
C0040736
reinjection of ≥ 2.106 cd34/kg
Beschrijving

Reinjection CD34 stem cell count

Datatype

boolean

Alias
UMLS CUI [1,1]
C0444600
UMLS CUI [1,2]
C1277788
patients hospitalized in the investigator center throughout the procedure until recovery from aplasia (pnn > 0.5 g/l)
Beschrijving

Hospitalization | Aplasia Recovery | Polymorphonuclear neutrophil Count

Datatype

boolean

Alias
UMLS CUI [1]
C0019993
UMLS CUI [2,1]
C0243065
UMLS CUI [2,2]
C2004454
UMLS CUI [3,1]
C0027950
UMLS CUI [3,2]
C0750480
mandatory affiliation with a health insurance system
Beschrijving

Affiliation mandatory Health Insurance

Datatype

boolean

Alias
UMLS CUI [1,1]
C1510825
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0021682
patients able to understand, read and write french
Beschrijving

Comprehension French language | Able to read French language | Able to write French language

Datatype

boolean

Alias
UMLS CUI [1,1]
C0233733
UMLS CUI [1,2]
C0376246
UMLS CUI [2,1]
C0586740
UMLS CUI [2,2]
C0376246
UMLS CUI [3,1]
C0584993
UMLS CUI [3,2]
C0376246
signed, written informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
tbi during conditioning
Beschrijving

Whole-Body Irradiation During Conditioning

Datatype

boolean

Alias
UMLS CUI [1,1]
C0043162
UMLS CUI [1,2]
C0347984
UMLS CUI [1,3]
C0376450
severe intolerance to the growth factor under study, or hypersensitivity to one of their components
Beschrijving

Intolerance Severe Growth Factor Study | Intolerance Severe Growth Factor Component

Datatype

boolean

Alias
UMLS CUI [1,1]
C0231199
UMLS CUI [1,2]
C0205082
UMLS CUI [1,3]
C0018284
UMLS CUI [1,4]
C2603343
UMLS CUI [2,1]
C0231199
UMLS CUI [2,2]
C0205082
UMLS CUI [2,3]
C0018284
UMLS CUI [2,4]
C1705248
immunosuppressive syndrome
Beschrijving

Immunosuppression

Datatype

boolean

Alias
UMLS CUI [1]
C4048329
pregnant or lactating women
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
difficult follow-up
Beschrijving

Follow-up Difficult

Datatype

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C0332218
documented history of cognitive or psychiatric disorders
Beschrijving

Cognition Disorders | Mental disorders

Datatype

boolean

Alias
UMLS CUI [1]
C0009241
UMLS CUI [2]
C0004936
participation or consideration of participation in another biomedical study during the follow-up period of the present trial.
Beschrijving

Study Subject Participation Status | Biomedical Research | Consideration Participation Biomedical Research

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0005540
UMLS CUI [3,1]
C0518609
UMLS CUI [3,2]
C0679823
UMLS CUI [3,3]
C0005540
Terug naar het begin van de pagina

Similar models

Eligibility Lymphoma NCT00794261

1 Formulieren
  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00794261
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
male or female patients aged ≥ 18 years
boolean
C0001779 (UMLS CUI [1])
Lymphoma | Multiple Myeloma
Item
patients with histologically confirmed lymphoma or myeloma
boolean
C0024299 (UMLS CUI [1])
C0026764 (UMLS CUI [2])
High-dose chemotherapy
Item
treatment with high-dose chemotherapy before inclusion
boolean
C1328050 (UMLS CUI [1])
Melphalan High dose | Multiple Myeloma
Item
intensification with high dose melphalan for patients with myeloma
boolean
C0025241 (UMLS CUI [1,1])
C0444956 (UMLS CUI [1,2])
C0026764 (UMLS CUI [2])
Transplantation Conditioning | Exception Whole-Body Irradiation First Relapse Hodgkin Disease | Other Coding | Consolidation therapy Quantity
Item
whatever the conditioning regimen, except tbi for patients with 1st relapse of hodgkin's lymphoma or with mnhl nb: patients having received two intensification courses are eligible if there has been more than 100 days between courses.
boolean
C0376450 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0043162 (UMLS CUI [2,2])
C4054953 (UMLS CUI [2,3])
C0019829 (UMLS CUI [2,4])
C3846158 (UMLS CUI [3])
C1511484 (UMLS CUI [4,1])
C1265611 (UMLS CUI [4,2])
Primary sclerosing cholangitis Autologous Transplantation
Item
autologous psc transplantation at the time of inclusion
boolean
C0566602 (UMLS CUI [1,1])
C0040736 (UMLS CUI [1,2])
Reinjection CD34 stem cell count
Item
reinjection of ≥ 2.106 cd34/kg
boolean
C0444600 (UMLS CUI [1,1])
C1277788 (UMLS CUI [1,2])
Hospitalization | Aplasia Recovery | Polymorphonuclear neutrophil Count
Item
patients hospitalized in the investigator center throughout the procedure until recovery from aplasia (pnn > 0.5 g/l)
boolean
C0019993 (UMLS CUI [1])
C0243065 (UMLS CUI [2,1])
C2004454 (UMLS CUI [2,2])
C0027950 (UMLS CUI [3,1])
C0750480 (UMLS CUI [3,2])
Affiliation mandatory Health Insurance
Item
mandatory affiliation with a health insurance system
boolean
C1510825 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0021682 (UMLS CUI [1,3])
Comprehension French language | Able to read French language | Able to write French language
Item
patients able to understand, read and write french
boolean
C0233733 (UMLS CUI [1,1])
C0376246 (UMLS CUI [1,2])
C0586740 (UMLS CUI [2,1])
C0376246 (UMLS CUI [2,2])
C0584993 (UMLS CUI [3,1])
C0376246 (UMLS CUI [3,2])
Informed Consent
Item
signed, written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Whole-Body Irradiation During Conditioning
Item
tbi during conditioning
boolean
C0043162 (UMLS CUI [1,1])
C0347984 (UMLS CUI [1,2])
C0376450 (UMLS CUI [1,3])
Intolerance Severe Growth Factor Study | Intolerance Severe Growth Factor Component
Item
severe intolerance to the growth factor under study, or hypersensitivity to one of their components
boolean
C0231199 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0018284 (UMLS CUI [1,3])
C2603343 (UMLS CUI [1,4])
C0231199 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0018284 (UMLS CUI [2,3])
C1705248 (UMLS CUI [2,4])
Immunosuppression
Item
immunosuppressive syndrome
boolean
C4048329 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Follow-up Difficult
Item
difficult follow-up
boolean
C3274571 (UMLS CUI [1,1])
C0332218 (UMLS CUI [1,2])
Cognition Disorders | Mental disorders
Item
documented history of cognitive or psychiatric disorders
boolean
C0009241 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
Study Subject Participation Status | Biomedical Research | Consideration Participation Biomedical Research
Item
participation or consideration of participation in another biomedical study during the follow-up period of the present trial.
boolean
C2348568 (UMLS CUI [1])
C0005540 (UMLS CUI [2])
C0518609 (UMLS CUI [3,1])
C0679823 (UMLS CUI [3,2])
C0005540 (UMLS CUI [3,3])
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