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CTRI Number  CTRI/2025/10/096712 [Registered on: 31/10/2025] Trial Registered Prospectively
Last Modified On: 31/10/2025
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Ayurveda 
Study Design  Single Arm Study 
Public Title of Study   Clinical study on Bhujangasana Practice and Buttermilk with Rock salt in patients having symptoms of Agnimandhya ( Indigestion) 
Scientific Title of Study   Clinical evaluation of Bhujangasana and Saindhavyukta takra in Agnimandhya (Indigestion) 
Trial Acronym  Nil 
Secondary IDs if Any  
Secondary ID  Identifier 
Nil  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Mohit Singh  
Designation  PG Scholar  
Affiliation  Uttaranchal Ayurvedic College and Hospital  
Address  Department of Swasthvritta and Yoga Uttaranchal Ayurvedic College and Hospital 17 old Mussoorie road Rajpur Dehradun Uttarakhand Uttaranchal 248009 India

Dehradun
UTTARANCHAL
248009
India 
Phone  8923306195  
Fax    
Email  singhmohitpundir567@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Smita Zambare  
Designation  Professor and HOD 
Affiliation  Uttaranchal Ayurvedic College and Hospital  
Address  Department of Swasthvritta and Yoga Uttaranchal Ayurvedic College and Hospital 17 old Mussoorie road Rajpur Dehradun Uttarakhand Uttaranchal 248009 India

Dehradun
UTTARANCHAL
248009
India 
Phone  8879133317  
Fax    
Email  smitazambare1@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Mohit Singh  
Designation  PG Scholar  
Affiliation  Uttaranchal Ayurvedic College and Hospital  
Address  Department of Swasthvritta and Yoga Uttaranchal Ayurvedic College and Hospital 17 old Mussoorie road Rajpur Dehradun Uttarakhand Uttaranchal 248009 India

Dehradun
UTTARANCHAL
248009
India 
Phone  8923306195  
Fax    
Email  singhmohitpundir567@gmail.com  
 
Source of Monetary or Material Support  
Uttaranchal Ayurvedic College and Hospital 196/2 Rajpur Road near Sai Mandir Rajpur Dehradun 248001 Dehradun Uttarakhand India 
 
Primary Sponsor  
Name  Mohit Singh  
Address  Uttaranchal Ayurvedic College and Hospital 17 old Mussoorie road Rajpur Dehradun Uttarakhand Uttaranchal 248009 
Type of Sponsor  Other [Self] 
 
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 Mohit Singh   Room No. 118 OPD of Swasthyarakshan and Yoga Uttaranchal Ayurvedic Hospital   196/2 Rajpur Road near Sai Mandir Rajpur Dehradun 248001 Uttarakhand India
Dehradun
UTTARANCHAL 
8923306195

singhmohitpundir567@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethical Commitee Uttaranchal Ayurvedic College and PG Research center  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition:K30||Functional dyspepsia. Ayurveda Condition: MANDAGNIH/ AGNISADA,  
 
Intervention / Comparator Agent  
snoIntervention/ComparatorTypeDrug-TypeProcedure NameDetails
1Comparator ArmDrugClassical(1) Medicine Name: Saindhav lavan and Takra, Reference: C.CH.15/117-119 Saindhav lavan-A.H.06/144, Route: Oral, Dosage Form: Panak/ Sharbat, Dose: 125(ml), Frequency: bd, Bhaishajya Kal: Adhobhakta, Duration: 60 Days, anupAna/sahapAna: No, Additional Information: -Take 125 ml Takra with 1gm of saindhav lavan after food.
 
Inclusion Criteria  
Age From  20.00 Year(s)
Age To  50.00 Year(s)
Gender  Both 
Details  1-Individual having mild digestive problems.
2-Individual who were fully co-operative for the study.
3-Individual with informed consent to participate in the study. 
 
ExclusionCriteria 
Details  1- Individual not willing for the trial.
2-Patient suffering from moderate to severe G.I.T.Disease.
3- Patients undergoing any abdominal surgical procedure.
4- Patients not addicted to Tobacco, Smoking,and Alcohol.
5- Individual taking any medicine for indigestion and acidity. 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
To assess the effect of saindhav yukta takra and Bhujangasana practice on Indigestion.  1-Baseline at day first before onset of treatment.
2-Followup after every fifteen day.
3- Two months after onset of treatment. 
 
Secondary Outcome  
Outcome  TimePoints 
Nil  Nil 
 
Target Sample Size   Total Sample Size="50"
Sample Size from India="50" 
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)   16/12/2025 
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)   Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
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   Agnimandhya or digestive impairment is prevalent condition affecting millions world wide leading to various GIT disorders.
Saindhavyukta Takra is traditional ayurvedic formulation has been mentioned in ancient text for its potential benefits in enhancing digestive fire and alleviating symptoms of agnimandhya.
Salected Drug and Yoga- Saindhav lavan mix with Takra and Bhujangasana practice.
Form of Medicine- 125ml they were given Sadyomatita Takra twice a day
Time Of administration- After intake a food
Procedure of Taking drug- The patients will be advice to mix 1-2gm or according to taste of Saindhav lavan in 125ml of instant buttermilk.
Route of administration- Oral
Duretion- 60 days
Follow up- Once a 15days
 
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