ID
11991
Description
Safety & Efficacy of Lamivudine & Tenofovir to Lower Plasma Level of Viral RNA in Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT01528865 Principal Investigator: Scott D Gitlin, MD
Link
https://clinicaltrials.gov/show/NCT01528865
Keywords
Versions (1)
- 8/30/15 8/30/15 -
Uploaded on
August 30, 2015
DOI
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License
Creative Commons BY 4.0
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Eligibility Lymphoma NCT01528865
Eligibility Lymphoma NCT01528865
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI-1
- C0680251
Description
chemotherapy; radiotherapy
Data type
boolean
Alias
- UMLS CUI [1]
- C3665472
- UMLS CUI [2]
- C1522449
Description
Have not recovered from the adverse effects or toxicities of lymphoma therapy most recently administered.
Data type
boolean
Alias
- UMLS CUI [1]
- C0879626
- UMLS CUI [2]
- C0087111
Description
Currently receiving any other investigational medication or therapy.
Data type
boolean
Alias
- UMLS CUI [1]
- C0013230
Description
Patients with a second malignancy that might interfere with interpretation of the results of this study.
Data type
boolean
Alias
- UMLS CUI [1]
- C0085183
Description
Patients with known allergic reaction to lamivudine or tenofovir disoproxil fumarate (DF).
Data type
boolean
Alias
- UMLS CUI [1]
- C1527304
- UMLS CUI [2]
- C1099776
Description
Patients on drugs that interfere with renal function or drugs that compete with tenofovir for active binding sites (i.e. intravenous cidofovir, acyclovir, ganciclovir, and valganciclovir).
Data type
boolean
Alias
- UMLS CUI [1]
- C1547774
- UMLS CUI [2]
- C0232804
Description
Uncontrolled concurrent illnesses, including, but not limited to, active/ongoing infection, symptomatic congestive heart failure, unstable angina pectoris.
Data type
boolean
Alias
- UMLS CUI [1]
- C0205420
- UMLS CUI [2]
- C0012634
Description
Women who are pregnant, become pregnant, or are breast-feeding.
Data type
boolean
Alias
- UMLS CUI [1]
- C0549206
- UMLS CUI [2]
- C0006147
Description
Standard blood tests that are positive for HIV infection
Data type
boolean
Alias
- UMLS CUI [1]
- C0745002
Similar models
Eligibility Lymphoma NCT01528865
- StudyEvent: Eligibility
C0011900 (UMLS CUI [2])
C0599161 (UMLS CUI [2])
C0175969 (UMLS CUI [2])
C0600061 (UMLS CUI [2])
C0812399 (UMLS CUI [3])
C1522449 (UMLS CUI [2])
C0087111 (UMLS CUI [2])
C1099776 (UMLS CUI [2])
C0232804 (UMLS CUI [2])
C0012634 (UMLS CUI [2])
C0006147 (UMLS CUI [2])