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Study identifier: NCT06410352 Synced from ClinicalTrials.gov · July 28, 2026
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Effectiveness of Weight Loss Methods on Lifespan for Metabolic Syndrome

Condition: Metabolic Syndrome  ·  Sponsor: University Medical Center, Kazakhstan

PhasePhase 4
Planned participants220
Who can joinAll sexes, 35 Years to 65 Years
Healthy volunteersNo

About this study

Background. The prevalence of type 2 diabetes mellitus (T2D) in the world is constantly increasing. Treatment of T2D is complicated by arterial hypertension and obesity (metabolic syndrome - MS). Cardiovascular complications are the main cause of death in patients with MS. Objective weight loss improves clinical and laboratory parameters in patients with T2D and hypertension. Purpose: To study lifespan, glycemic and lipid metabolism, quality of life, and cost-effectiveness of pharmacologic, surgical, and dietetic weight loss methods in obese patients with MS at 24 weeks in a comparative clinical trial. Methods: 1. st stage - Study design: An open pilot prospective clinical trial. The study included 71 adult patients with T2D and hypertension for the Ramadan fast's (RF) weight loss. 2. nd stage - Study design: A 24-week open label, prospective, multicenter, comparative clinical trial with the intention-to-treat analysis. Participants. Totally 150 adult patients with MS aged 35-65 years and with BMI≥27 kg/m2 for Asian will be included. They will be distributed in three comparative groups: drug treatment, surgery and diet. Primary endpoints: weight loss, fasting blood glucose, blood insulin level, systolic/diastolic BP. Secondary endpoints: blood lipids, heel bone mineral density (HBMD), and ejection fraction (EF). Expected results: A prospective multicenter clinical study will provide comparative results on life expectancy, glycemic and lipid metabolism, quality of life…

This description comes directly from the study's public registry record.

Talk to the study team

full-professor Kuat Oshakbayev  ·  +77013999394  ·  okp.kuat@gmail.com

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Locations (1)

Kuat Pernekulovich OshakbayevAstana, Astana, KazakhstanRecruiting

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Source record: clinicaltrials.gov/study/NCT06410352