Efficacy and safety of HT048 and HT077 for body fat and weight loss in overweight adults A study protocol for a double-blind, randomized, placebo-controlled trial

被引:4
作者
Song, Jungbin [1 ]
Shin, Seon-mi [2 ]
Kim, Hocheol [1 ]
机构
[1] Kyung Hee Univ, Coll Korean Med, Dept Herbal Pharmacol, 26 Kyungheedae Ro, Seoul 02447, South Korea
[2] Semyung Univ, Coll Korean Med, Dept Internal Med, 65 Semyung Ro, Jecheon Si 27136, Chungcheongbuk, South Korea
关键词
antiobesity; Citrus unshiu; clinical trial; Crataegus pinnatifida; Nelumbo nucifera; overweight; Prunus persica; NELUMBO-NUCIFERA LEAVES; ALL-CAUSE MORTALITY; METABOLIC SYNDROME; VISCERAL FAT; MASS INDEX; OBESITY; CONSTITUENTS; FLAVONOIDS; EXTRACT;
D O I
10.1097/MD.0000000000017922
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The prevalence of excessive body weight has rapidly increased worldwide over the past decades; however, medications are intended for moderately and severely obese patients and are associated with side effects. As an alternative approach, the use of traditional herbal medicines has gained increasing popularity among overweight individuals in recent years in East Asia. HT048 is an herbal extract of Citrus unshiu and Crataegus pinnatifida, and HT077 is an herbal extract of Nelumbo nucifera and Prunus persica. These 4 herbs have been used widely for body weight reduction in China and Korea. The aims of this trial are to investigate whether HT048 and HT077 are effective at reducing body fat and weight in overweight adults, and to determine the safety of HT048 and HT077. Methods/design: A double-blind, randomized, placebo-controlled, 3-arm parallel group trial will be conducted in adults with a body mass index (BMI) of 25 to <30kg/m(2). A total of 120 eligible participants will be randomized in a 1:1:1 ratio to receive either HT048 (1000 mg), HT077 (400 mg), or matching placebo twice daily for 12 weeks, and will be monitored for an additional 4-week follow-up period after the treatment. All participants will be assessed for efficacy and safety of the investigational product at baseline and weeks 4, 8, 12, and 16. The primary endpoint is the change in body fat mass and percent body fat measured by dual-energy Xray absorptiometry at week 12 from the baseline. The secondary efficacy variables are abdominal fat area measured by computed tomography, body fat mass and percent body fat measured by bioelectrical impedance analysis, body weight, BMI, and serum lipids and adipocytokines concentrations. Safety will be evaluated on the basis of reported adverse events, abnormal laboratory results, vital signs, and physical examination findings. Discussion: This is a first-in-human trial of HT048 and HT077 to assess the efficacy and safety in overweight subjects. The results will provide high-quality evidence of the therapeutic benefits of HT048 and HT077 for weight management and the prevention of obesity.
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页数:7
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