Department of Internal Diseases, Nephrology and Dialysis, Military Institute of Medicine - National Research Institute
Warsaw, Masovian District, 04-141, Poland
Location status: Recruiting
NCT Number: NCT05716880
The goal of this non-commercial clinical trial is to assess efficacy and safety of ketoanalogues of essential amino acids in the prevention of protein-energy wasting in nephrotic syndrome.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 3
Warsaw, Masovian District, 04-141, Poland
Location status: Recruiting
Adult patients with new diagnosis or relapse of nephrotic syndrome and glomerular filtration rate of ≥ 30 mL/min/1.73m2 will be included in the study. Exclusion criteria will be a secondary cause of nephrotic syndrome, morbid obesity and severe diseases affecting nutritional status.
Participants will be randomly assigned to the intervention group (KA+MPD) or control group (MPD); randomization will be stratified by type of glomerular disease (podocytopathy or other type) and investigational site. The control group will follow the diet recommended in nephrotic syndrome - a medium protein diet (MPD) - under the care of a dietitian. Intervention group will receive Ketosteril (1 tablet for every 5 kg of ideal body weight) as an addition to the diet. All patients will also receive treatment for underlying glomerular disease in accordance with current guidelines and local practice.
The main objective is to assess the efficacy of Ketosteril as an add-on therapy in preventing the loss of lean tissue mass (LTM) over 6 months compared to a standard diet.
The additional aims include the assessment of muscle function parameters, nephrotic syndrome severity and laboratory indicators of catabolism.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Daily dose = 1 tabl / 5 kg of ideal body weight
MPD: daily protein intake of 0.8-1.0 g/kg of ideal body weight + up to 5 g based on daily proteinuria
Time frame: 6 months
The difference between the initial lean tissue mass (LTM) and the lowest LTM measured within 6 months, expressed in percentage. The non-inferiority hypothesis of Ketosteril use will be tested as the primary endpoint.
LTM will be measured with bioimpedance spectroscopy.
Time frame: 6 months
The difference between the initial lean tissue mass (LTM) and the lowest LTM measured within 6 months, expressed in percentage. The superiority hypothesis of Ketosteril use will be tested as the secondary endpoint.
Time frame: 6 months
The percentage of patients meeting criteria of nephrotic syndrome-associated protein-energy wasting (neph-PEW): reduction of LTM by 3% within 3 months or by 5% within 6 months.
Time frame: 6 months
Change in distance walked in the 6-minute walk test from baseline value; expressed in meters.
Time frame: 6 months
Change in HGS value from baseline; expressed in kg.
Time frame: 6 months
Change in serum albumin level from baseline value; expressed in g/dL.
Time frame: 6 months
Change in uPCR value from baseline; expressed in mg/g.
Time frame: 6 months
Change in serum LDL level from baseline; expressed in mg/dL.
Time frame: 6 months
Change in serum triglycerides level from baseline; expressed in mg/dL.
Time frame: 6 months
Change in serum uric acid level from baseline; expressed in mg/dL.
Time frame: 12 months
The percentage of patients who experienced the unfavorable disease course including: glomerular disease related death; venous or arterial thromboembolic event; infection requiring hospital admission; acute kidney injury in the stage 2 or 3; sustained glomerular filtration rate reduction over 50% or initiation of kidney replacement therapy; unplanned hospital admission due to complications of nephrotic syndrome treatment.
Time frame: 12 months
Change in glomerular filtration rate from baseline; expressed in mL/min/1.73m2.
Interested in participating?
Request InfoMilitary Institute od Medicine National Research Institute
Other
FORMA - a Multicenter Randomized-controlled Trial to Evaluate the Efficacy and Safety of Ketoanalogues of Essential Amino Acids in Prophylaxis of Protein-energy Wasting in Nephrotic Syndrome
Acronym: FORMA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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