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CTRI Number  CTRI/2025/03/082463 [Registered on: 17/03/2025] Trial Registered Prospectively
Last Modified On: 18/03/2026
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Nutraceutical 
Study Design  Randomized, Parallel Group, Placebo Controlled Trial 
Public Title of Study   A study to evaluate the efficacy of two different mixes of HMO-2-O-fucosyllactose + Humiome Post LB postbiotic (postbiotic-LB) on Gastrointestinal Symptoms in individuals with Irritable Bowel Syndrome (IBS) 
Scientific Title of Study   A randomized, placebo-controlled, double-blind clinical study to evaluate the efficacy of two different mixes of HMO-2-O-fucosyllactose (HMO-2FL) + Humiome Post LB postbiotic (postbiotic-LB) on Gastrointestinal Symptoms in individuals with Irritable Bowel Syndrome (IBS) 
Trial Acronym  nil 
Secondary IDs if Any  
Secondary ID  Identifier 
2023-08-14-DORP Version: 2.0 Date 7th jan 2025  Protocol Number 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Sanjay Vaze 
Designation  Sr.Manager-Clinical Development 
Affiliation  Vedic Lifesciences Pvt Ltd 
Address  Vedic Lifesciences Pvt Ltd 118 B Morya House off New Link Road Andheri West Mumbai Mumbai (Suburban) Mumbai (Suburban) MAHARASHTRA

Mumbai (Suburban)
MAHARASHTRA
400053
India 
Phone  8655670964  
Fax    
Email  sanjay.v@vediclifesciences.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Sanjay Vaze 
Designation  Sr.Manager-Clinical Development 
Affiliation  Vedic Lifesciences Pvt Ltd 
Address  Vedic Lifesciences Pvt Ltd 118 B Morya House off New Link Road Andheri West Mumbai Mumbai (Suburban) Mumbai (Suburban) MAHARASHTRA

Mumbai (Suburban)
MAHARASHTRA
400053
India 
Phone  8655670964  
Fax    
Email  sanjay.v@vediclifesciences.com  
 
Details of Contact Person
Public Query

Modification(s)  
Name  Harshad K More 
Designation  Assistant Project Lead-Clinical Operations 
Affiliation  Vedic Lifesciences Pvt Ltd 
Address  Vedic Lifesciences Pvt Ltd 118 B Morya House off New Link Road Andheri West Mumbai Mumbai (Suburban) Mumbai (Suburban) MAHARASHTRA

Mumbai (Suburban)
MAHARASHTRA
400053
India 
Phone  8655793246  
Fax    
Email  harshad.m@vediclifesciences.com  
 
Source of Monetary or Material Support  
Vedic Lifesciences Pvt. Ltd. 118-B, Morya House, off New Link Road, Andheri West Mumbai –400053, Maharashtra, India 
 
Primary Sponsor
Modification(s)  
Name  DSM Firmenich Switzerland Ltd 
Address  Wurmisweg 576 CH-4303 Kaiseraugst Switzerland  
Type of Sponsor  Other [self] 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study
Modification(s)  
No of Sites = 19  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Amol Kulkarni  Aster Aadhar Hospital  Aster Aadhar Hospital, Near, R. S. No. 628, B Ward, near KMT Workshop, Shastri Nagar, Kolhapur, Maharashtra - 416012.
Kolhapur
MAHARASHTRA 
9130463328

kamul102468@gmail.com  
Dr Nikhil Jillawar  Bhakti Siddhant Hospital  Bhakti Siddhant Hospital, Plot. No. 217, Sector 21, Opp. Sai Mandir, Yamunanagar, Nigdi, Pune-411044, Maharashtra, India.
Pune
MAHARASHTRA 
9099058141

nikhiljillawar@gmail.com 
Dr Deepak Ahire   D Y Patil  D Y Patil Hospital, Medical college and research centre, Nerul, sector 5, Navi Mumbai, Thane 400706
Thane
MAHARASHTRA 
0909908113

dipakahire33@gmail.com 
Dr Bharat Kumar Jain  Dhanwantri Hospital   339-c Madaliar Rd, Next to kaka halwai rasta peth, Pune, Maharashtra 411002
Pune
MAHARASHTRA 
8087448919

dr_bharatjain@rediffmail.com 
Dr Manish Kumar Singh   Ford Hospital  Ford Hospital, Samne Ghat Rd, Balaji Nagar, Colony, Varanasi, Uttar Pradesh 221005.
Varanasi
UTTAR PRADESH 
8227991508

drmks13@yahoo.com 
Dr Naresh Kumar Bansal  Gastro and Liver Clini  Gastro and Liver Clinic, 170A, Dada Satram Mamtani Marg, Block C4H, Janakpuri, Delhi, 110058
South West
DELHI 
9310246832

drnbansal@ymail.com 
Dr Mahesh Mahadik  Gastro Hub Hospital  Gastrohub Hospital, Royal Radiance Survey No 18, Hissa no 11/5, Pune , Maharashtra 411027
Pune
MAHARASHTRA 
9890819432

maheshkood@gmail.com 
Dr Sameer Kumar   Gleneagles Hospital  Gleneagles Hospital, 6-1-1040/1 to 4, Lakdikapul, Hyderabad, Telangana 500004
Hyderabad
TELANGANA 
8860031692

sameerzidane@gmail.com 
Dr Nikhil Prabhu  Haut Diabetes Care  Bhaveshwar Plaza,505-506 A-wing 5th floor Shreyas signal Ghatkopar -West 400086
Mumbai
MAHARASHTRA 
9870916962

dr.nikhilprabhu@gmail.com 
Dr Pankaj Singh Jadon  Jaipur National University Institute of Medical Sciences and Research Centre  Jaipur National University Institute of Medical Sciences and Research Centre Jaipur-Agra Bypass, Near New RTO Office, Jagatpura, Jaipur-302017
Jaipur
RAJASTHAN 
9799902222

Drpankaj.medicine@jnujaipur.ac.in 
Dr Nikhil Patil  Jeevan Clinic  1st, Floor, Borgaonkar avenue, Opp, sai hall, Wayle nagar, Khadakpada, Kalyan-W, Thane, 421301 Maharashtra.
Thane
MAHARASHTRA 
9870916962

dr.nikhilprabhu@gmail.com 
Dr Mahesh Thakare  Omkar Ear Nose Throat Hospital & Research Centre  SK Empire, Near Ved Mandir, Mico Circle, Trimbak Road, Nashik -422002.
Nashik
MAHARASHTRA 
7822821643

Mahesh131090@gmail.com 
Dr Adeshkumar Andhale  Pawana Hospiatl  Gat No 167 Urse Parandadi Road Taluka near Talegaon Dhabhade Somatne Phata Maval Maharashtra 410506
Pune
MAHARASHTRA 
7057895232

nishikant.pawanahospital@gmail.com  
Dr Hemant Kumar Gupta  Samvedna Hospital  Samvedna Hospital 827/88C, Ravidrapuri, Varanasi, Uttar Pradesh -221005. lndia
Varanasi
UTTAR PRADESH 
9415316365

hemantg26@yahoo.com 
Dr Kushal Bangar  Shivam Hospital  Shivam Hospital; Plot no. 57, C.R.W. CHS, Near M.I.D.C, water tank, Kalyan Road, Dombivli (East), 421201
Mumbai
MAHARASHTRA 
9545664884

dr.kushal.bangar83@gmail.com  
Dr Vijayalakshmi  Shri. B. M. Patil Medical College, Hospital and Research Centre  B.L.D.E. (DEEMED to be University) Shri. B. M. Patil Medical College, Hospital and Research Centre, Vijayapur, Smt. Bangaramma Sajjan Campus, Sholapur Road, Bijapur – 586103, Karnataka, India.
Bijapur
KARNATAKA 
8792793848

dr.viju21@yahoo.in 
Dr Amar Raykantiwar   Silver brich multispeciality hospital  20/10/11, U.P.D.Construction,S.No.6, Plot No.1 To Plot No.4, Dhayari Road, near Sawatamali Mandir, Narhe, Pune, Maharashtra 411041
Pune
MAHARASHTRA 
84519410150

dr.amarray26@gmail.com 
Dr Pratibha Sonawane  Soham Hospital  Archit,Sai Avenue,Shree Vallabh Nagar, Behind old chhan Hotel,Mumbai Naka,Nashik-422001
Nashik
MAHARASHTRA 
7738080952

drpratibha.clinizestresearch@gmail.com 
Dr Kiran Shinde  Vishwaraj hospital  Vishwaraj hospital, Near Loni Railway station Loni Kalbhor, Solapur - Pune Hwy, Pune, Maharashtra 412201
Pune
MAHARASHTRA 
9986003257

dr.kiranshinde@gmail.com 
 
Details of Ethics Committee
Modification(s)  
No of Ethics Committees= 19  
Name of Committee  Approval Status 
Altezza Institutional Ethics Committee  Approved 
Aster Aadhar Ethics Committee  Approved 
Central Independent Ethics Committee  Approved 
Central Independent Ethics Committee   Approved 
Central Independent Ethics Committee CIEC  Approved 
Ethicare ethics Committee  Approved 
Ethicare ethics Committee  Approved 
FORD HOSPITAL ETHICS COMMITTEE  Approved 
Good Society for Ethical Research,  Approved 
IEC for biomedical and health research  Approved 
IEC Gleneagles Hospitals  Approved 
IEC of MAEERs Vishwaraj hospital  Approved 
Instituitional Ethics Committee JNU Institute for Medical Sciences and Research Centre  Approved 
Institutional Ethics Committee for Human research at BLDEUs University  Approved 
Jivenrekha Institutional Ethics Committee   Approved 
Lakeview Ethics Committee  Not Applicable 
Muktai Hospital Ethics Committee  Approved 
Samvedna Hospital Ethics Committee  Approved 
Supreme Independent Ethics Committee  Not Applicable 
 
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,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  Microcrystalline cellulose (MCC): 300 mg  1 capsule per day will be taken orally for 6 week after breakfast  
Intervention  Mix -01 Humiome® Post LB postbiotic (postbiotic-LB): 300 mg •Human Milk Oligosaccharides 2’-O-fucosyllactose (HMO-2FL): 300 mg  1 capsule per day will be taken orally for 6 weeks, after breakfast 
Comparator Agent  MIX-2 •Humiome® Post LB postbiotic (postbiotic-LB) 100 mg •Human Milk Oligosaccharides 2’-O-fucosyllactose (HMO-2FL): 500 mg  1 capsule per day will be taken orally for 6 weeks , after breakfast 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  70.00 Year(s)
Gender  Both 
Details  1.Written informed consent will be obtained before any study-related assessments
2.Male or female aged less than or equal to 18 to 70 years at the time of consent
3.Female individuals of childbearing potential (Females who are peri or post-menopausal ,when there has been no or irregular menstruation for a minimum of 12 months prior to screening, are considered not to be of child-bearing potential.), who are not surgically sterilized, must have a negative pregnancy test at screening and be willing to practice one of the following appropriate contraceptive methods until the last visit
i.Sexual abstinence
ii.Oral contraceptives.
iii.Trans-dermal patches or depot injection of a progestogen drug (starting at least 4 weeks prior to product administration).
iv.Double barrier method: condom or occlusive cap plus spermicidal agent.
Intrauterine device intrauterine system subdermal implant, or vaginal ring (placed at least 4 weeks prior to product administration/2 weeks prior screening).
vi. Contraceptives must be effective before the randomization visit
4.Individuals with Plasma FBG (fasting blood glucose) (less than equal to 125 mg/dl).
5.Individuals with haemoglobin Hb (more than equal to 10 g/dl).
6.Individuals with BP (blood pressure) (less than equal to 140/100 mm Hg)
7.Individuals with normal haematology as assessed by CBC (complete blood counts)
8.Individuals with TSH levels in between 0.4 mIU/L and 5.0 mIU/L
9.SGOT and SGPT within 2 X the Upper normal limit (ULN) and serum creatinine within 1.5 X ULN
10.Rome-IV diagnostic criteria: Individuals with more than 25% of bowel movements with Bristol stool types 1, 2 or 6,7 and have had recurrent abdominal pain, on average, at least 1 day/week in the last 3 months. The pain is associated with two or more of the following criteria:
a.Related to defecation
b.Associated with a change in frequency of stool
c.Associated with a change in form or appearance of stool as assessed by Bristol stool type 1,2, 6 or 7
11.Abdominal pain severity (more than equal to 6 on a 11-point scale) at screening and during placebo run-in period.
12.Individuals with IBS-SSS score of at least 175 points at screening.
13.Individuals who are mentally stable as assessed by Perceived stress Scale (PSS) less than equal to 26 (Low to Moderate stress)
14.Individuals who understand the nature and purpose of the study including the potential risks and side effects.
15.Individuals who are willing to complete all study procedures including study related questionnaires and comply with study requirements.
16.Individuals who are capable of filling the app-based digital form/diary.
 
 
ExclusionCriteria 
Details  1.Individuals with IBS-M.
2.Treatment with an investigational drug within 30 days/5 half-lives of the drug (whichever longest) prior to screening visit.
3.Individuals with organic disease like infectious diseases, inflammatory diseases, metabolic disorders, neurological diseases, autoimmune disorders, cancer
4.Individuals with a history of surgical resection of the stomach, small intestine or large intestine.
5.Individuals with a history of or complications from inflammatory bowel disease , colitis and enteritis.
6.Individuals with a history of any diet-based intolerance (gluten or lactose intolerance).
7.Individuals with a history of drug or alcohol abuse within the past 6 months.
8.Individuals with severe depression or an anxiety disorder, which could potentially affect the efficacy evaluation (as determined by the qualified investigator).
9.Individuals with uncontrolled hypertension or on antihypertensive medications
10.Individuals with serious cardiovascular diseases, respiratory diseases, renal diseases, hepatic diseases, gastrointestinal diseases (excluding IBS), blood diseases or neurological or psychiatric diseases.
11.Individuals who are pregnant, breastfeeding or planning on becoming pregnant throughout the course of the study.
12.Individuals with Type I or Type II diabetes mellitus.
13.Individuals with a history of or current diagnosis of any cancer diagnosed less than 5 years prior to screening. Individuals with cancer in full remission more than 5 years after diagnosis are acceptable.
14.Individuals who are immuno-compromised (HIV positive, on anti-rejection medication, rheumatoid arthritis and other autoimmune disorders).
15.Individuals with a history of abdominal surgery.
16.Individuals with diarrhoea of any other origin.
17.Individuals currently or in future planning to fast for more than 24 hours.
18.Individuals with an active eating disorder.
19.Individuals who have used an over-the-counter or prescription laxative medication or any other herbal agents affecting GI motility within 2 weeks prior to screening.
20.Individuals who have used pre/pro/post/synbiotic, Human Milk Oligosaccharides (HMOs), or fiber supplements (or probiotic/fiber enriched foods) or FODMAP diet or an antibiotic within 4 weeks prior to screening.
21.Individuals who have used IBS specific treatments within 4 weeks prior to screening.
22.Individuals who currently consume greater than 2 standard alcoholic drinks per day from past 3 months. (One unit of alcohol is equal to 45 ml of hard liquor, 150 ml of wine or a pint of beer)
23.Smokers (in any number and any format)
24.Individuals with an allergy or sensitivity to the probiotic products.
25.Individuals who are cognitively impaired and/or who are unable to give an informed consent.
26.Individuals who have abnormal laboratory results or any other medical or psychological condition which, in the opinion of the qualified investigator, may adversely affect the Individuals’ ability to complete the study or its measures or which may pose significant risk to the individual.
 
 
Method of Generating Random Sequence   Stratified block randomization 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Participant and Investigator Blinded 
Primary Outcome  
Outcome  TimePoints 
To assess the efficacy of 6 weeks of daily consumption of two different mixes of HMO 2’-O-fucosyllactose (HMO-2FL) + Humiome® Post LB postbiotic (postbiotic-LB) on IBS symptoms as assessed by IBS Symptom Severity Scale (IBS-SSS), when compared to placebo in individuals with IBS   Day 0, and Day 42 
 
Secondary Outcome  
Outcome  TimePoints 
To assess the efficacy of daily consumption of two different mixes of HMO 2’-O-fucosyllactose (HMO-2FL) + Humiome® Post LB postbiotic (postbiotic-LB) on IBS symptoms as assessed by IBS Symptom Severity Scale (IBS-SSS), when compared to placebo in individuals with IBS  Day 0, Day 21 
To assess the efficacy of 6 weeks of daily consumption of two different mixes of HMO 2’-O-fucosyllactose (HMO-2FL) + Humiome® Post LB postbiotic (postbiotic-LB); on IBS symptoms as assessed by IBS-SSS, when compared to baseline in individuals with IBS  Day 0, Day 21 and Day 42 
To assess the efficacy of 6 weeks of daily consumption of two different mixes of HMO 2’-O-fucosyllactose (HMO-2FL) + Humiome® Post LB postbiotic (postbiotic-LB); on the following parameters compared to baseline, each other and placebo in individuals with IBS
1.Abdominal pain severity (11-point scale)
2.Stool consistency (Bristol Stool Form Scale type 3, 4 & 5).
3.Quality of Life (QOL) score as assessed by IBS- QoL questionnaire.
4.Abdominal bloating as assessed by GIQLI (Gastrointestinal Quality of Life Index)
5.Percentage of responders to the treatment based on improvement on primary objective
 
Day 0, Day 21 and Day 42 
To assess the efficacy of 6 weeks of daily consumption of two different mixes of HMO 2’-O-fucosyllactose (HMO-2FL) + Humiome® Post LB postbiotic (postbiotic-LB); on the following parameters compared to baseline, each other and placebo in individuals with IBS
1.Daily number of stools (stool frequency).
2.Absolute difference in rescue medication consumption in active and placebo groups.
3.Number of adverse events.
4.Subjective global assessment of IP tolerability by participants. 
Throughout the study 
To assess the efficacy of 6 weeks of daily consumption of two different mixes of HMO 2’-O-fucosyllactose (HMO-2FL) + Humiome® Post LB postbiotic (postbiotic-LB); on the following parameters compared to baseline, each other and placebo in individuals with IBS
1.IBS-related mental stress relief as assessed by the Perceived Stress Scale (PSS)
2.Gut Permeability assessment (Lactulose to Mannitol ratio test) [to be conducted in 30 participants in each arm]
3.Stool pH & redox [to be conducted in those participants who are undergoing LMR (lactulose-to-mannitol ratio) in 30 participants each arm] 
Day 0 and Day 42 
To assess the efficacy of 6 weeks of daily consumption of two different mixes of HMO 2’-O-fucosyllactose (HMO-2FL) + Humiome® Post LB postbiotic (postbiotic-LB); on the following parameters compared to baseline, each other and placebo in individuals with IBS
1.Change in gut microbiome composition at genus and/ or species level.
2.Change in microbiome diversity.
3.Changes in fecal metabolomics profile.
4.Changes in organic acids in fecal samples (acetate, propionate, butyrate, valerate, lactate). 
Day 0 and Day 42 
 
Target Sample Size   Total Sample Size="330"
Sample Size from India="330" 
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)   29/03/2025 
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="1"
Days="1" 
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   The present study is a randomized, double-blind, placebo-controlled, parallel group three arm study. The intervention duration for all the study participants is 6 weeks 
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