School of Psychology and Exercise Science, Murdoch University, Perth, WA, 6150, Australia.
Samvedna Hospital, B-27 88G, Ravindrapuri, New Colony, Varanasi, U.P, 221005, India.
BMC Complement Altern Med. 2018 Mar 20;18(1):98. doi: 10.1186/s12906-018-2168-y.
To evaluate the efficacy and tolerability of a poly-herbal formulation, Herbagut, for the treatment of gastrointestinal symptoms and its effect on quality of life parameters in patients presenting with self-reported, unsatisfactory bowel habits.
This was a randomised, double-blind, placebo-controlled trial. Fifty adults with self-reported unsatisfactory bowel habits, primarily characterised by chronic constipation were randomly allocated to take Herbagut or a matching placebo for 28 days. Efficacy of gastrointestinal changes was measured by the completion of a patient daily diary evaluating changes in stool type (Bristol Stool Form Scale), ease of bowel movements, and feeling of complete evacuation; and the Gastrointestinal Symptom Rating Scale (GSRS). Changes in quality of life were also examined using the World Health Organization Quality of Life - abbreviated version (WHOQOL-BREF), and the Patient Assessment of Constipation-Quality of Life (PAC-QOL).
All participants completed the 28-day trial with no adverse events reported. Compared to the placebo, weekly bowel movements increased over time (p < .001), as did self-reported, normal bowel motions (76% vs 4%; p < .001). Self-reported incomplete evacuation was also lower in the Herbagut group compared to placebo (24% vs 76%; p = <.001). GSRS domain ratings for abdominal pain, constipation, diarrhoea, indigestion, and reflux also decreased significantly in people taking Herbagut compared to placebo (p < .001, for all domains). Moreover, quality of life significantly improved in the Herbagut group compared to placebo as indicated by significantly greater improvement in WHOQOL-BREF domain ratings for overall quality of life, social relations, environmental health, psychological health, and physical health (p < .001, for all domains); and PAC-QOL domain ratings for physical discomfort, psychosocial discomfort, worries and concerns, and life satisfaction (p < .001, for all domains). The changes were considered clinically meaningful as evidenced by their large effect sizes.
Herbagut ingestion over a 28-day period resulted in improvements in several gastrointestinal symptoms and overall quality of life. Further investigation utilising larger sample sizes and diverse clinical and cultural populations are needed.
Clinical Trials Registry- India /2016/11/007479 . Registered 24 April 2015 (retrospectively registered).
评估一种复方草药制剂 Herbagut 治疗胃肠道症状的疗效和耐受性,并观察其对自述排便习惯不佳的患者生活质量参数的影响。
这是一项随机、双盲、安慰剂对照试验。50 名自述排便习惯不佳的成年人(主要表现为慢性便秘)被随机分配服用 Herbagut 或匹配的安慰剂,疗程 28 天。通过患者每日日记评估粪便类型(布里斯托粪便形态量表)、排便通畅程度和排空感的变化,以及胃肠道症状评分量表(GSRS)来评估胃肠道变化的疗效。使用世界卫生组织生活质量简表(WHOQOL-BREF)和患者便秘生活质量量表(PAC-QOL)也评估了生活质量的变化。
所有参与者均完成了 28 天的试验,未报告不良事件。与安慰剂相比,每周排便次数随时间增加(p<0.001),自报正常排便次数也增加(76%比 4%;p<0.001)。Herbagut 组自报不完全排空的比例也低于安慰剂组(24%比 76%;p=0.001)。与安慰剂相比,服用 Herbagut 的患者腹部疼痛、便秘、腹泻、消化不良和反流的 GSRS 各域评分也显著降低(所有域均 p<0.001)。此外,与安慰剂相比,Herbagut 组的生活质量显著改善,WHOQOL-BREF 整体生活质量、社会关系、环境卫生、心理健康和身体健康各域评分的改善更明显(所有域均 p<0.001);PAC-QOL 躯体不适、心理社会不适、担忧和顾虑以及生活满意度各域评分的改善也更明显(所有域均 p<0.001)。由于其具有较大的效应量,这些变化被认为具有临床意义。
Herbagut 摄入 28 天后,胃肠道症状和整体生活质量均有改善。需要进一步开展更大样本量、不同临床和文化人群的研究。
印度临床试验注册处/2016/11/007479。注册日期 2015 年 4 月 24 日(追溯注册)。