ID

32551

Description

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

Keywords

  1. 11/6/18 11/6/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

November 6, 2018

DOI

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License

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
Description

Inclusion Criteria

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

Informed Consent

Data type

boolean

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

Age

Data type

boolean

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

Protocol Compliance

Data type

boolean

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

T-Cell Lymphoma

Data type

boolean

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

Peripheral T-Cell Lymphoma Subtype Any

Data type

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.
Description

Cutaneous t-cell lymphoma/Mycosis fungoides

Data type

boolean

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

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

Data type

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.
Description

Combination Chemotherapy Quantity

Data type

boolean

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

Exclusion Criteria

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

Cutaneous T-cell lymphoma/Sezary Syndrome

Data type

boolean

Alias
UMLS CUI [1]
C0036920

Similar models

Eligibility T-cell Non-Hodgkin's Lymphoma NCT00655668

Name
Type
Description | Question | Decode (Coded Value)
Data type
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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