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一项随机、双盲、安慰剂对照、单中心的比较研究,评估Phaseolean®在超重/肥胖参与者中的安全性和有效性。

A randomized, double-blinded, placebo-controlled, single-center, comparative study evaluating Phaseolean® safety and efficacy in overweight/obese participants.

作者信息

Singh Shashi Chandrama, Singh Harshpal, Choudhary Muskan

机构信息

Research and Development Centre, Ambe Phytoextracts Pvt. Ltd. Pauri Garhwal, Uttarakhand, 246276, India.

出版信息

Heliyon. 2024 Jul 24;10(15):e35144. doi: 10.1016/j.heliyon.2024.e35144. eCollection 2024 Aug 15.

Abstract

SCOPE

Phaseolean®, a standardized water extract of or white kidney bean, exhibits α-amylase inhibitory property, which decreases calorie absorption by preventing or delaying carbohydrate digestion, thus supporting weight management. This randomized, double-blind, placebo-controlled, single-center comparative study (Clinical trial registration number: CTRI/2023/02/049440, Registered on: February 03, 2023) evaluated the safety and efficacy of Phaseolean® in weight management in overweight or obese participants upon regular intake at two different doses compared with placebo.

METHOD

Sixty-six participants were enrolled and randomly divided into three groups, considering the inclusion & exclusion criteria. Each group was assigned a specific daily dosage for three meals: Phaseolean® 1500 mg/day (500 mg per meal), Phaseolean® 3000 mg/day (1000 mg per meal), or placebo 1500 mg/day (500 mg per meal), administered thrice a day before meals for 45 consecutive days. Body weight; body mass index (BMI); skinfold fat thickness; waist, hip, and thigh circumferences; and blood biochemical parameters were monitored and analyzed to evaluate the effects of these interventions.

RESULTS AND CONCLUSIONS

Of the 66 enrolled participants, 62 completed the study. Treatment with Phaseolean® 1500 mg/day reduced the weight by an average of 2.10 kg (0.33 kg/week), while that with 3000 mg/day was 1.94 kg (0.30 kg/week); 0.13 kg weight loss (0.02 kg/week) was observed in the placebo group after 45 days, showing significant differences between the Phaseolean® and placebo groups (p < 0.01). BMI, body fat, skinfold fat thickness, and the waist, hip, and thigh circumference were significantly reduced (p < 0.01) in both Phaseolean® groups compared with those in the placebo group, which showed no significant changes.No adverse effects were observed during the clinical trial period. Phaseolean® 1500 mg/day dose was more effective in weight reduction than the 3000 mg/day higher dose. Therefore, Phaseolean® can be used to support healthy weight management.

摘要

范围

Phaseolean®是一种标准化的菜豆或白芸豆水提取物,具有α-淀粉酶抑制特性,可通过预防或延缓碳水化合物消化来减少热量吸收,从而有助于体重管理。这项随机、双盲、安慰剂对照、单中心比较研究(临床试验注册号:CTRI/2023/02/049440,注册日期:2023年2月3日)评估了与安慰剂相比,超重或肥胖参与者定期服用两种不同剂量的Phaseolean®进行体重管理的安全性和有效性。

方法

根据纳入和排除标准招募了66名参与者,并将其随机分为三组。每组被分配特定的每日三餐剂量:Phaseolean®1500毫克/天(每餐500毫克)、Phaseolean®3000毫克/天(每餐1000毫克)或安慰剂1500毫克/天(每餐500毫克),每天饭前服用三次,连续服用45天。监测并分析体重、体重指数(BMI)、皮褶脂肪厚度、腰围、臀围和大腿围以及血液生化参数,以评估这些干预措施的效果。

结果与结论

66名纳入研究的参与者中,62名完成了研究。每天服用1500毫克Phaseolean®可使体重平均减轻2.10千克(0.33千克/周),而每天服用3000毫克的减轻量为1.94千克(0.30千克/周);45天后,安慰剂组体重减轻0.13千克(0.02千克/周),Phaseolean®组与安慰剂组之间存在显著差异(p<0.01)。与安慰剂组相比,两个Phaseolean®组的BMI、体脂、皮褶脂肪厚度以及腰围、臀围和大腿围均显著降低(p<0.01),而安慰剂组无显著变化。临床试验期间未观察到不良反应。每天1500毫克剂量的Phaseolean®在减重方面比3000毫克/天的高剂量更有效。因此,Phaseolean®可用于支持健康的体重管理。

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