A Novel Herbal Composition Alleviates Functional Constipation, Reduces Gastrointestinal Transit Time, and Improves Bowel Function in Adults: A Double-Blind, Randomized Clinical Study.

IF 6.8 4区 医学 Q1 NUTRITION & DIETETICS
Gaurav Singh, Indresh Dixit, Douglas Kalman, Naga Tejaswi Gogineni
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Abstract

Background and objective: A recent proof-of-concept pilot clinical study has demonstrated that consumption of CL18100F4, a proprietary herbal blend of Withania somnifera root and Abelmoschus esculentus fruit extracts, significantly relieved the participants from functional constipation and improved their quality of life. The objective of the present randomized, double-blind, placebo-controlled study was to reevaluate the efficacy and tolerability of CL18100F4 in a larger number of subjects.

Methods: Male and female subjects (n = 135; age: 25-60 years), selected through Rome-IV criteria for functional constipation, were randomized into placebo and 300 or 500 mg of CL18100F4 groups and supplemented daily over 60 consecutive days. The primary efficacy outcome measure was Patient Assessment of Constipation-Symptoms (PAC-SYM), evaluated at baseline and on days 7, 30, and 60 of supplementation. The secondary efficacy parameters included Patient Assessment of Constipation-Quality of Life (PAC-QOL), Gastrointestinal Symptom Rating Scale (GSRS) scores, Gastrointestinal Transit Time (GIT), and Complete Spontaneous Bowel Movement (CSBM). Serum levels of Interleukin (IL)-6, IL-10, cortisol, gastrin, serotonin, Diamine oxidase (DAO), and Zonulin were measured.

Results: CL18100F4 supplementation significantly (p < 0.001) reduced the PAC-SYM, PAC-QOL, GSRS scores, and GIT and improved CSBM scores. CL18100F4 significantly improved (p < 0.001) sleep quality and decreased depression and anxiety symptoms in the participants. Notably, relief in constipation symptoms and improved gastrointestinal (GI) function were reported starting from day 7. Furthermore, CL18100F4 supplementation significantly (p < 0.001) increased the serum levels of IL-10, DAO, serotonin, gastrin, reduced IL-6, cortisol, and Zonulin. No major adverse events were observed. Participants' vital signs, hematology, clinical biochemistry, and urinalysis parameters were within the normal ranges.

Conclusion: The present investigation demonstrates that CL18100F4 is tolerable and efficacious in relieving functional constipation, alleviating GI dysfunction, and improving associated non-GI factors in male and female adults.

一种新型草药成分可缓解成人功能性便秘、缩短胃肠转运时间并改善排便功能:双盲随机临床研究》。
背景和目的:最近的一项概念验证试验性临床研究表明,服用由睡莲根和槟榔果提取物混合而成的专有草药 CL18100F4 能明显缓解参与者的功能性便秘,并改善他们的生活质量。本随机、双盲、安慰剂对照研究的目的是在更多受试者中重新评估 CL18100F4 的疗效和耐受性:男性和女性受试者(n = 135;年龄:25-60 岁)根据功能性便秘的 Rome-IV 标准筛选,随机分为安慰剂组和 300 或 500 毫克 CL18100F4 组,连续 60 天每天补充。主要疗效指标是患者便秘症状评估(PAC-SYM),在基线和补充剂服用第 7、30 和 60 天进行评估。次要疗效参数包括便秘患者生活质量评估(PAC-QOL)、胃肠道症状评分量表(GSRS)评分、胃肠道转运时间(GIT)和完全自发性排便(CSBM)。测量了血清中白细胞介素(IL)-6、IL-10、皮质醇、胃泌素、5-羟色胺、二胺氧化酶(DAO)和Zonulin的水平:结果:补充 CL18100F4 有显著效果(p p p 结论):本研究表明,CL18100F4 对缓解功能性便秘、减轻消化道功能障碍以及改善男女成人的相关非消化道因素具有良好的耐受性和疗效。
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