ID

32551

Beschrijving

A Phase II Study of Single-Agent Lenalidomide in Subjects With Relapsed Or Refractory T-Cell Non-Hodgkin's Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00655668

Link

https://clinicaltrials.gov/show/NCT00655668

Trefwoorden

  1. 06-11-18 06-11-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

6 november 2018

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility T-cell Non-Hodgkin's Lymphoma NCT00655668

Eligibility T-cell Non-Hodgkin's Lymphoma NCT00655668

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
must understand and voluntarily sign an informed consent form.
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
must be ≥ 18 years of age at the time of signing the informed consent form.
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
must be able to adhere to the study visit schedule and other protocol requirements.
Beschrijving

Protocol Compliance

Datatype

boolean

Alias
UMLS CUI [1]
C0525058
biopsy-proven t-cell non-hodgkin's lymphoma, either:
Beschrijving

T-Cell Lymphoma

Datatype

boolean

Alias
UMLS CUI [1]
C0079772
peripheral t-cell lymphoma (ptcl) whatever the subtype, or
Beschrijving

Peripheral T-Cell Lymphoma Subtype Any

Datatype

boolean

Alias
UMLS CUI [1,1]
C0079774
UMLS CUI [1,2]
C0449560
UMLS CUI [1,3]
C1552551
cutaneous t-cell lymphoma (ctcl), but only the subtype mycosis fungoides.
Beschrijving

Cutaneous t-cell lymphoma/Mycosis fungoides

Datatype

boolean

Alias
UMLS CUI [1]
C0026948
relapsed or refractory to previous therapy for t-cell non-hodgkin's lymphoma.
Beschrijving

Prior Therapy | T-cell lymphoma recurrent | T-cell lymphoma refractory

Datatype

boolean

Alias
UMLS CUI [1]
C1514463
UMLS CUI [2]
C0854826
UMLS CUI [3]
C0854827
must have received at least one prior combination chemotherapy regimen. there is no limit on the number of prior therapies.
Beschrijving

Combination Chemotherapy Quantity

Datatype

boolean

Alias
UMLS CUI [1,1]
C1521750
UMLS CUI [1,2]
C1265611
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
cutaneous t-cell lymphoma of subtype sézary syndrome.
Beschrijving

Cutaneous T-cell lymphoma/Sezary Syndrome

Datatype

boolean

Alias
UMLS CUI [1]
C0036920

Similar models

Eligibility T-cell Non-Hodgkin's Lymphoma NCT00655668

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
must understand and voluntarily sign an informed consent form.
boolean
C0021430 (UMLS CUI [1])
Age
Item
must be ≥ 18 years of age at the time of signing the informed consent form.
boolean
C0001779 (UMLS CUI [1])
Protocol Compliance
Item
must be able to adhere to the study visit schedule and other protocol requirements.
boolean
C0525058 (UMLS CUI [1])
T-Cell Lymphoma
Item
biopsy-proven t-cell non-hodgkin's lymphoma, either:
boolean
C0079772 (UMLS CUI [1])
Peripheral T-Cell Lymphoma Subtype Any
Item
peripheral t-cell lymphoma (ptcl) whatever the subtype, or
boolean
C0079774 (UMLS CUI [1,1])
C0449560 (UMLS CUI [1,2])
C1552551 (UMLS CUI [1,3])
Cutaneous t-cell lymphoma/Mycosis fungoides
Item
cutaneous t-cell lymphoma (ctcl), but only the subtype mycosis fungoides.
boolean
C0026948 (UMLS CUI [1])
Prior Therapy | T-cell lymphoma recurrent | T-cell lymphoma refractory
Item
relapsed or refractory to previous therapy for t-cell non-hodgkin's lymphoma.
boolean
C1514463 (UMLS CUI [1])
C0854826 (UMLS CUI [2])
C0854827 (UMLS CUI [3])
Combination Chemotherapy Quantity
Item
must have received at least one prior combination chemotherapy regimen. there is no limit on the number of prior therapies.
boolean
C1521750 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Cutaneous T-cell lymphoma/Sezary Syndrome
Item
cutaneous t-cell lymphoma of subtype sézary syndrome.
boolean
C0036920 (UMLS CUI [1])

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