FULL DETAILS (Read-only)  -> Click Here to Create PDF for Current Dataset of Trial
CTRI Number  CTRI/2025/09/094192 [Registered on: 03/09/2025] Trial Registered Prospectively
Last Modified On: 02/04/2026
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Drug
Ayurveda
Screening 
Study Design  Single Arm Study 
Public Title of Study   Outcomes of Capsule Fenugreek in Gastrointestinal problems in T2DM patients 
Scientific Title of Study   Evaluating Gastrointestinal Effects Of Fenugreek In Patients Suffering From T2DM 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Supriya Bhalerao 
Designation  Associate Professor and Head 
Affiliation  Interactive Research School For Health Affairs Bharati Vidyapeeth (Deemed to be) University 
Address  Bharati Vidyapeeth Educational Campus, Pune Satara Road, Pune, 411043 Pune Maharashtra 411043 India

Pune
MAHARASHTRA
411043
India 
Phone  9527589516  
Fax    
Email  supriya.bhalerao@bharatividyapeeth.edu  
 
Details of Contact Person
Scientific Query
 
Name  Dr Supriya Bhalerao 
Designation  Associate Professor and Head 
Affiliation  Interactive Research School For Health Affairs Bharati Vidyapeeth (Deemed to be) University 
Address  Bharati Vidyapeeth Educational Campus, Pune Satara Road, Pune, 411043 Pune Maharashtra 411043 India

Pune
MAHARASHTRA
411043
India 
Phone  9527589516  
Fax    
Email  supriya.bhalerao@bharatividyapeeth.edu  
 
Details of Contact Person
Public Query
 
Name  Dr Kartikey T Jagtap 
Designation  Research Assistant 
Affiliation  Interactive Research School for Health AffairsBharati Vidyapeeth (Deemed to be) University 
Address  Bharati Vidyapeeth Educational Campus, Pune Satara Road, Pune 411 043 Bharati Vidyapeeth Educational Campus, Pune Satara Road, Pune 411 043 Pune MAHARASHTRA 411043 India

Pune
MAHARASHTRA
411043
India 
Phone  9158265928  
Fax    
Email  kartikey.jagtap@bharatividyapeeth.edu  
 
Source of Monetary or Material Support  
Interactive Research School for Health Affairs (IRSHA), Bharati Vidyapeeth (Deemed to be University), Pune 
 
Primary Sponsor  
Name  Bharati Vidyapeeth Minor Research Project 
Address  Bharati Vidyapeeth (Deemed to be) Unoversity, Educational Campus, Pune Satara Road, 411043 Pune Maharashtra India 
Type of Sponsor  Research institution 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Madhavi Mahajan   Bharati Hospital and Research Centre   OPD no.4, Kayachikitsa department(Medicine), Ground floor, Bharati Ayurveda College, Pune, Maharasthra, Pincode 411043 Pune MAHARASHTRA
Pune
MAHARASHTRA 
9860124248

madhavi.mahajan@bharatividyapeeth.edu 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
INSTITUTIONAL ETHICS COMMITTEE [BV(DU)COA-IEC]  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition:K929||Disease of digestive system, unspecified. Ayurveda Condition: GAURAVA-KSHIRADOSHAH,  
 
Intervention / Comparator Agent  
snoIntervention/ComparatorTypeDrug-TypeProcedure NameDetails
1Intervention ArmLifestyle--Dinacarya: NA, Ritucarya: NA, Acara Rasayana:NA, Other:NA, Pathya/Apathya:yes, Pathya:Laghupachya Ahara, Ushna Jala Pana, Shakahara , Apathya:Ati-Amla, Lavan, Katu Rasa Ahara, Guru, Abhishyandi Ahara, ratri jagrana
2Intervention ArmDrugOther than Classical(1) Medicine Name: Fenugreek powder capsule, Reference: NA, Route: Oral, Dosage Form: Capsules, Dose: 500(mg), Frequency: bd, Bhaishajya Kal: Pragbhakta, Duration: 3 Months, anupAna/sahapAna: Yes(details: -taking with water), Additional Information: -
 
Inclusion Criteria  
Age From  30.00 Year(s)
Age To  60.00 Year(s)
Gender  Both 
Details  1. Individuals with HbA1c less than or equal to 9 per cent with or without complications based on clinical examination and the investigator’s discretion.

2. 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.

3. Individuals willing to abide by the study-related procedures
 
 
ExclusionCriteria 
Details  1. Individuals on insulin therapy.

2. Individuals with acute gastric symptoms like appendicitis, intestinal obstruction, etc. and chronic gastric symptoms of hyperacidity.

3. 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. 

4. Individuals with a known history of endocrinological disorders, cardiac, liver or renal  pathologies  

5. Individuals with a known history of psychiatric/ psychological disorders 

6. Pregnant or lactating females
 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Open Label 
Primary Outcome  
Outcome  TimePoints 
1. Improvement in Gastrointestinal symptoms.
2. Improvement in Glycemic profile.
3. No change in the safety parameters. 
Day 0, Day 7, Day 15, Day 30, Day 45, Day 60, Day 75, Day 90 
 
Secondary Outcome  
Outcome  TimePoints 
NIL  NIL 
 
Target Sample Size   Total Sample Size="30"
Sample Size from India="30" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)   01/10/2025 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Open to Recruitment 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  
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.
 
Close