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临床试验/CTRI/2025/09/094192
CTRI/2025/09/094192尚未招募不适用

Evaluating Gastrointestinal Effects Of Fenugreek In Patients Suffering From T2DM

Bharati Vidyapeeth Minor Research Project1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年10月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
1. Improvement in Gastrointestinal symptoms.

研究概览

简要总结

Title:

Evaluation of Trigonella foenum-graecum (Fenugreek) on Gastrointestinal Symptoms and Glycemic Control in Patients with Type 2 Diabetes Mellitus

Background:

Type 2 Diabetes Mellitus (T2DM) is frequently associated with gastrointestinal (GI) complications such as gastroparesis, constipation, bloating, and dyspepsia. Anti-diabetic medications like Metformin, Glimepiride, and Voglibose also cause GI side effects. These factors adversely affect quality of life and glycemic management.

Fenugreek (Trigonella foenum-graecum), widely used in Indian diets and described in Ayurveda as Prameha nashaka (anti-diabetic), has shown hypoglycemic, appetite-regulating, and GI-modulating properties. Preliminary studies suggest improvement in appetite, bowel movements, and a favorable trend in glucose control with Fenugreek.

Rationale:

There is limited research on the effect of Fenugreek on GI symptoms and gut hormones in T2DM. This study aims to explore its role as a safe, culturally acceptable adjunct in diabetes management.

Objectives:

To evaluate the effect of Fenugreek on GI symptoms in patients with T2DM

To assess its impact on glycemic profile (fasting glucose, postprandial glucose, HbA1c, insulin)

To evaluate safety through clinical monitoring and laboratory tests

Study Design:

Type: Single-arm, exploratory clinical study

Sample size: 36 patients (30 completed, considering 20 percent dropout)

Setting: Recruitment from College of Ayurveda; procedures at IRSHA, Bharati Vidyapeeth University, Pune

Intervention: Fenugreek seed powder standardized, roasted, and compressed into 500 mg tablets. Patients will take 3 g/day (3 tablets twice daily before meals) for 3 months

Follow-up: Monthly clinical visits (Day 30, 60, 90) and telephonic check-ins

Eligibility:

Inclusion:T2DM patients (30-55 years), HbA1c less than or equal to 9 percent, GI complaints (bloating, fullness, nausea, constipation for one month or more)

Exclusion: Insulin therapy, acute gastric or intestinal disorders, concurrent herbal or nutritional supplements, severe organ dysfunction, psychiatric disorders, pregnancy or lactation, participation in another trial

Assessments:

Clinical and Questionnaires: Agni (Ayurvedic digestion scale), Diabetes Bowel Syndrome Questionnaire (DBSQ), Simplified Nutritional Appetite Questionnaire (SNAQ)

Biochemical: Fasting and postprandial glucose, HbA1c, fasting insulin, Liver Function Test, Renal Function Test, Complete Blood Count

Anthropometry and Body Composition: Weight, BMI, waist circumference

Safety: Adverse events, rescue medication if required

Data Analysis:

Parametric data: Mean plus/minus SD, Paired t-test

Non-parametric data: Median (Range), Wilcoxon signed-rank test

Categorical data: Chi-square test

Statistical significance at p less than 0.05

Expected Outcome:

Fenugreek supplementation may reduce GI symptoms, improve appetite and bowel habits, and support better glycemic control, while being safe and well-tolerated. Stored serum samples may provide further insights into GI hormone mechanisms.

Societal and National Relevance:

The study addresses India’s rising diabetes burden by investigating a culturally accepted, diet-based Ayurvedic intervention. It supports national missions on integrating traditional medicine into modern healthcare, with the potential to improve quality of life and reduce medication-related GI side effects.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
30.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • •Individuals with HbA1c less than or equal to 9 per cent with or without complications based on clinical examination and the investigator’s discretion.
  • •Individuals with gastrointestinal complaints, viz., flatulence, epigastric or post-prandial fullness, bloating, nausea, and constipation occurring on and off over the period of 1 month or more.
  • •Individuals willing to abide by the study-related procedures.

排除标准

  • •Individuals on insulin therapy.
  • •Individuals with acute gastric symptoms like appendicitis, intestinal obstruction, etc.
  • •and chronic gastric symptoms of hyperacidity.
  • •Individuals with a known history of usage of herbal medications/ nutritional supplements/ multivitamin supplements/ pre and probiotic supplementation within the past 30 days for any indication.
  • •Individuals with a known history of endocrinological disorders, cardiac, liver or renal pathologies
  • •Individuals with a known history of psychiatric/ psychological disorders
  • •Pregnant or lactating females.

结局指标

主要结局

1. Improvement in Gastrointestinal symptoms.

时间窗: Day 0, Day 7, Day 15, Day 30, Day 45, Day 60, Day 75, Day 90

2. Improvement in Glycemic profile.

时间窗: Day 0, Day 7, Day 15, Day 30, Day 45, Day 60, Day 75, Day 90

3. No change in the safety parameters.

时间窗: Day 0, Day 7, Day 15, Day 30, Day 45, Day 60, Day 75, Day 90

次要结局

未报告次要终点

研究者

发起方
Bharati Vidyapeeth Minor Research Project
申办方类型
Research institution
责任方
Principal Investigator
主要研究者

Dr Supriya Bhalerao

Interactive Research School For Health Affairs Bharati Vidyapeeth (Deemed to be) University

研究点 (1)

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