Peroral Supplemental Nutrition in End-stage Renal Disease With and Without HIV Comorbidity
- Conditions
- End-Stage Renal Disease
- Interventions
- Dietary Supplement: peroral high-caloric supplemental nutritionDietary Supplement: peroral supplemental nutrition
- Registration Number
- NCT00687050
- Lead Sponsor
- Johann Wolfgang Goethe University Hospital
- Brief Summary
End-stage renal disease is often accompanied by malnutrition due to less appetite, metabolic changes or both. Human immunodeficiency virus-infection may exacerbate the state of malnutrition. In a pilot study, we recruit both HIV invected and non-infected patients on hemodialysis. Non-HIV patients will be randomized to peroral supplemental nutrition or no peroral supplemental nutrition. All HIV patients will receive peroral supplemental nutrition. The nutritional state will be determined in magnet resonance tomography at the start and at the end of the study (muscle diameter of triceps m.) and with laboratory parameters (plasma albumin and others). The hypothesis is that supplemental peroral nutrition (a total 250 kcal per day) will stop loss of muscle mass in end-stage renal disease patients (compared to their counterparts without supplemental peroral nutrition) as well as in the high risk group of HIV patients. This pilot study may lead to larger randomized clinical trials and, may affect dietary recommendations.
- Detailed Description
In end-stage renal disease (ESRD), cachexia is a common finding. Metabolic changes, malnutrition, or both appear to be the underlying problems. In fact, lean body mass per body weight better predicts prognosis than creatinin based models (NDT, 2004.19:1182). In addition, comorbidity such as HIV infection may exacerbate cachexia found in ESRD. Whether or not daily supplemental, high-caloric nutrition in ESRD corrects a catabolic state in ESRD is unclear.
Hypothesis to be tested:
Daily supplemental high-caloric nutrition beneficially affects cytokine stimulation (TNF alpha, IL 1beta, IL 6, CrP) and nutritional state (cross sectional area of triceps m. in mid-humerus position (MRT), plasma albumin) in in HIV-positive hemodialysis patients and in chronic hemodialysis patients compared to chronic hemodialysis patients without supplemental nutrition.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
- patients on hemodialysis for more than 1 year,
- Group 1: HIV infection
- patients on hemodialysis for less than 1 year,
- Group 2 and 3: HIV infection
- no pre-/post dialysis weight differences of > 3 kg after long HD free interval over last 10 HD sessions.
- no current high-caloric nutrition supplements or planned high-caloric supplements for clinical reasons.
- pregnancy
- for women: no use of oral contraceptives or other at least equally effective contraception in women with childbearing potential
- known neoplastic disease other than skin tumors (except melanoma)
- mental disease or retardation with impaired judgement power
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description 1 peroral high-caloric supplemental nutrition HIV-positive hemodialysis patients (as a high risk group for cachexia) will be given daily drinks of Renilon 7.5 (125 ml, 2 kcal/ml) as peroral supplemental nutrition on top to their recommended high-protein, high-caloric diet. 3 peroral supplemental nutrition Chronic hemodialysis patients randomized to peroral supplemental nutrition.
- Primary Outcome Measures
Name Time Method Cross sectional area of triceps m. in mid-humerus position (MRT) 6 months
- Secondary Outcome Measures
Name Time Method plasma albumin < 3.6 mg/dl 6 months
Trial Locations
- Locations (1)
Hospital of the Goethe University Frankfurt am Main
🇩🇪Frankfurt am Main, Germany