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HT048和HT077对超重成年人身体脂肪和体重减轻的疗效与安全性:一项双盲、随机、安慰剂对照试验的研究方案

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.

作者信息

Song Jungbin, Shin Seon-Mi, Kim Hocheol

机构信息

Department of Herbal Pharmacology, Kyung Hee University College of Korean Medicine, Dongdaemun-gu, Seoul.

Department of Internal Medicine, Semyung University College of Korean Medicine, Jecheon-si, Chungcheongbuk-do, Republic of Korea.

出版信息

Medicine (Baltimore). 2019 Nov;98(45):e17922. doi: 10.1097/MD.0000000000017922.

Abstract

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 <30 kg/m. 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 X-ray 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.

TRIAL REGISTRATION

Korean Clinical Research Information Service (KCT0004271) Registered September 2, 2019.

摘要

背景

在过去几十年里,全球超重的患病率迅速上升;然而,药物是用于中度和重度肥胖患者的,且伴有副作用。作为一种替代方法,近年来在东亚,使用传统草药在超重人群中越来越受欢迎。HT048是温州蜜柑和山楂的草药提取物,HT077是莲和桃的草药提取物。这四种草药在中国和韩国已被广泛用于减轻体重。本试验的目的是研究HT048和HT077是否能有效降低超重成年人的体脂和体重,并确定HT048和HT077的安全性。

方法/设计:将对体重指数(BMI)为25至<30 kg/m²的成年人进行一项双盲、随机、安慰剂对照的三臂平行组试验。总共120名符合条件的参与者将按1:1:1的比例随机分组,接受HT048(1000 mg)、HT077(400 mg)或匹配的安慰剂,每日两次,共12周,并在治疗后进行额外4周的随访监测。所有参与者将在基线以及第4、8、12和16周接受研究产品的疗效和安全性评估。主要终点是第12周时通过双能X线吸收法测量的体脂质量和体脂百分比相对于基线的变化。次要疗效变量包括通过计算机断层扫描测量的腹部脂肪面积、通过生物电阻抗分析测量的体脂质量和体脂百分比、体重、BMI以及血脂和脂肪细胞因子浓度。将根据报告的不良事件、异常实验室结果、生命体征和体格检查结果评估安全性。

讨论

这是HT048和HT077在人体中的首次试验,旨在评估其在超重受试者中的疗效和安全性。结果将为HT048和HT077在体重管理和预防肥胖方面的治疗益处提供高质量证据。

试验注册

韩国临床研究信息服务中心(KCT0004271),于2019年9月2日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48b2/6855614/e4aaecf05670/medi-98-e17922-g001.jpg

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