Bupropion for Depression in ESRD Patients on Hemodialysis
| Status: | Terminated |
|---|---|
| Conditions: | Depression, Depression, Renal Impairment / Chronic Kidney Disease, Renal Impairment / Chronic Kidney Disease, Major Depression Disorder (MDD) |
| Therapuetic Areas: | Nephrology / Urology, Psychiatry / Psychology, Pulmonary / Respiratory Diseases |
| Healthy: | No |
| Age Range: | 30 - 70 |
| Updated: | 7/19/2018 |
| Start Date: | March 31, 2016 |
| End Date: | March 1, 2018 |
The proposed study will evaluate the response and remission rates for major depressive
disorder (MDD) in end-stage renal disease (ESRD) patients undergoing maintenance hemodialysis
(HD) treated with bupropion or fluoxetine for 12 weeks. In addition, the study will document
the relative tolerability and safety, and longitudinally contrast the effects of bupropion
and fluoxetine on measures of cognitive function, fatigue, inflammation, and tryptophan (TRP)
and TRP catabolites in blood. It is hypothesized that both drugs will significantly reduce
MDD symptoms from baseline, and be tolerable and safe, but bupropion will be associated with
greater reduction in pro-inflammatory cytokines, cognitive impairment, and fatigue compared
with fluoxetine.
The Specific Aims of this study are:
Aim 1: Determine the efficacy of bupropion and fluoxetine in treatment of MDD in ESRD/HD
patients.
Aim 2: Determine whether longitudinal change in MDD symptoms, cognitive dysfunction, and
fatigue differ between bupropion and fluoxetine.
Aim 3: Determine whether longitudinal change in MDD symptoms, cognitive dysfunction, and
fatigue correlate with change in inflammation, measures of TRP availability to brain, or
neurotoxic TRP metabolites.
Hypotheses:
1. Bupropion and fluoxetine will both show efficacy in treating MDD;
2. Bupropion will lead to greater improvement in cognitive dysfunction and fatigue than
fluoxetine; and
3. Change in cognition and fatigue over time will correlate with change in c-reactive
protein (CRP) and quinolinic acid and change in overall depression score will correlate
with measures of TRP availability.
disorder (MDD) in end-stage renal disease (ESRD) patients undergoing maintenance hemodialysis
(HD) treated with bupropion or fluoxetine for 12 weeks. In addition, the study will document
the relative tolerability and safety, and longitudinally contrast the effects of bupropion
and fluoxetine on measures of cognitive function, fatigue, inflammation, and tryptophan (TRP)
and TRP catabolites in blood. It is hypothesized that both drugs will significantly reduce
MDD symptoms from baseline, and be tolerable and safe, but bupropion will be associated with
greater reduction in pro-inflammatory cytokines, cognitive impairment, and fatigue compared
with fluoxetine.
The Specific Aims of this study are:
Aim 1: Determine the efficacy of bupropion and fluoxetine in treatment of MDD in ESRD/HD
patients.
Aim 2: Determine whether longitudinal change in MDD symptoms, cognitive dysfunction, and
fatigue differ between bupropion and fluoxetine.
Aim 3: Determine whether longitudinal change in MDD symptoms, cognitive dysfunction, and
fatigue correlate with change in inflammation, measures of TRP availability to brain, or
neurotoxic TRP metabolites.
Hypotheses:
1. Bupropion and fluoxetine will both show efficacy in treating MDD;
2. Bupropion will lead to greater improvement in cognitive dysfunction and fatigue than
fluoxetine; and
3. Change in cognition and fatigue over time will correlate with change in c-reactive
protein (CRP) and quinolinic acid and change in overall depression score will correlate
with measures of TRP availability.
Inclusion Criteria:
- age 30-70 yrs;
- have patent and non-infected arteriovenous fistula or graft;
- are receiving maintenance HD 3 times per week lasting for 3-4 hours;
- serum albumin of ≥ 3.2 g/dl, serum phosphate of <6.5 mg/dl, and serum hemoglobin of ≥9
mg/dl in consecutive two blood tests as per the National Kidney Foundation Disease
Outcomes Quality Initiative (NKF KDOQI) guidelines [subjects failing screening due to
blood test will be allowed to be re-screened in 30 days];
- receiving stable or maintenance dose of iron or erythropoietin-stimulating agents,
statins, angiotension receptor blockers and/or angiotension converting enzyme
inhibitors, phosphate binders, vitamin D receptor analogs as these agents may
influence cytokines proposed in the study;
- meet the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV)
criteria for MDD;
- have a Ham-D score > 17
Exclusion Criteria:
- meet DSM-IV criteria for Bipolar Disorder or other psychotic disorder in the month
prior to screening;
- are taking antidepressants, anti-anxiety medications, or hypnotics (including Zyban
for smoking cessation);
- having failed to respond to or tolerate bupropion or fluoxetine in the past
- allergic to fluoxetine or bupropion
- known history of HIV/AIDS; No testing will be conducted for screening purposes
- known history of alcohol or drug abuse or dependence within the month prior to
screening based on clinical records;
- history of myocardial infarction or heart failure within one month of screening or a
history of seizures or stroke at any point;
- history of chronic liver disease and diagnosis of hepatic encephalopathy based on
clinical records;
- currently diagnosed with cancer or receiving any cancer treatment;
- history of any infection within the last 2 weeks ;
- currently taking any antibiotics, anti-inflammatory, and immune-modulator agents;
- recorded noncompliance with dialysis schedules; and
- currently participating in clinical or behavioral intervention studies.
- recorded noncompliance with dialysis schedules; and
- currently participating in clinical or behavioral intervention studies
We found this trial at
1
site
529 West Markham Street
Little Rock, Arkansas 72205
Little Rock, Arkansas 72205
(501) 686-7000
Principal Investigator: Pedro L Delgado, MD
Phone: 501-526-8140
University of Arkansas for Medical Sciences The University of Arkansas for Medical Sciences (UAMS) in...
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