Status:
TERMINATED
Trial To Evaluate the Efficacy of Oral Salsalate in the Treatment of Older Adults With Unexplained Anemia
Lead Sponsor:
Harvey Jay Cohen
Collaborating Sponsors:
National Institute on Aging (NIA)
Conditions:
Anemia
Eligibility:
All Genders
65+ years
Phase:
PHASE2
Brief Summary
The purpose of this study is to determine whether treatment of unexplained anemia in older adults and elevated inflammatory markers with oral salsalate can improve hemoglobin levels and improve physic...
Detailed Description
There is well-defined morbidity and mortality associated with anemia in the elderly and the increasing proportion of elderly adults underscores the population's attributable risk of anemia. As a poten...
Eligibility Criteria
Inclusion
- Understand and voluntarily sign an informed consent form
- Age 65 years and older, residing in the community or in an assisted-living facility
- Able to adhere to the study visit schedule and other protocol requirements
- Hemoglobin concentration ≥ 9.0 g/dL and \< 11.5 g/dL for women and ≥ 9.0 to \< 12.7 g/dL for men
- Unexplained anemia (See Appendix 2 for definitions of anemia diagnosis to determine anemia is unexplained)
- Serum IL-6 level ≥ 1.0 pg/mL obtained during screening period (performed at central laboratory).
- Must be able to understand and speak in English; or Spanish speaking subjects who do not speak English may be enrolled per local IRB process and approval, provided the site has appropriate bilingual study staff.
Exclusion
- Red blood cell transfusions within the past 3 months
- Estimated glomerular filtration rate (eGFR) of \< 30 ml/min (by abbreviated MDRD)
- Use of erythropoiesis stimulating agents (ESA) in the past 3 months
- Active infection defined as symptomatic, requiring active treatment (prophylaxis allowed) or hospitalized for \> 24 hours primarily for infection within the past month
- Uncontrolled hypertension defined as diastolic blood pressure \> 95 mm Hg or systolic blood pressure \> 160 mm Hg on 2 separate occasions during screening period
- Distance on 6MWT above the median for age and sex adjusted population medians (see Table 4)
- Other primary uncorrected cause for anemia including:
- Known active inflammatory disease including auto-immune diseases (e.g., systemic lupus erythematosis, rheumatoid arthritis, mixed connective tissue disease, sarcoidosis, bronchiolitis obliterans, vasculitis, polymyalgia rheumatica, temporal arteritis, inflammatory bowel disease or related diseases);
- Chronic active infection (e.g., HIV, viral hepatitis, tuberculosis, osteomyelitis) or receiving therapy within the past 3 months for chronic infection
- Acute infection within past 3 months (pneumonia, sepsis, bacteremia, prostatitis, urosepsis, pyelonephritis, cholecystitis)
- Receipt of immunosuppressive therapy in the past 2 years including prednisone except for topical therapy
- Any cancer (aside from non-melanoma skin cancer) in the past 2 years or on therapy for cancer. In addition, prostate cancer will be excluded if patients have metastatic disease, have had prostatectomy within the prior 6 months, have ever received external beam radiation therapy or brachytherapy, or have received androgen deprivation therapy in the prior 24 months. Subjects with a history of any other form of cancer will likewise be excluded if they have received any radiation or chemotherapy in the prior 24 months.
- Fecal Occult Blood Test positivity in the past 3 years, Gastrointestinal bleeding in past 3 years and history of peptic ulcer w/ evidence of bleeding
- Elevated AST or ALT ≥ 2x upper limit of normal
- Use of any other experimental drug or therapy within 28 days of initial screening visit
- History of moderate tinnitus affecting instrumental activities of daily activities in the past 3 months
- Current use of acetylsalicylic acid (aspirin) in doses greater than 82 mg/day in the past 3 months. Subjects will also be ineligible if they consume or are expected to consume non-steroidal anti-inflammatory drugs (NSAIDs), corticosteroids, methotrexate, furosemide or anticoagulants during the course of this study.
- Elevated thyroid stimulating hormone (TSH), or other signs of hypothyroid condition. Patients on a stable dose of thyroid replacement are eligible, providing TSH is not elevated.
- Seizure disorder for which phenytoin is used for treatment.
- Hypersensitivity to salsalate, salicylic acid, or acetylsalicylic acid
- History of transient ischemic attacks (TIA), cerebral vascular accident, a clinical diagnosis of angina or myocardial infarction, any coronary interventions (PCI, Bypass, Stent placement) within the prior 12 months to reduce the risk of subject requiring aspirin therapy during the trial
- Dementia defined as the inability to independently provide informed consent and a Montreal Cognitive Assessment (MoCA) score \< 22
Key Trial Info
Start Date :
March 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 1 2014
Estimated Enrollment :
11 Patients enrolled
Trial Details
Trial ID
NCT01506726
Start Date
March 1 2012
End Date
November 1 2014
Last Update
October 18 2016
Active Locations (12)
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1
Lakeview Medical Research
Summerfield, Florida, United States, 34491
2
St Joseph's/Candler Health System
Savannah, Georgia, United States, 31405
3
University of Illinois, Chicago
Chicago, Illinois, United States, 60612
4
University of Chicago Medical Center
Chicago, Illinois, United States, 60637