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CTRI Number  CTRI/2025/10/096711 [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   A clinical study on relief from Ajeerna (Indigestion) using Jeerak (Jeera) and Pashchimottanasana 
Scientific Title of Study   Clinical Evaluation of Jeerak and Pashchimottanasana Practice in Ajeerna (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  Yudhi Sharma 
Designation  MD Scholar 
Affiliation  Uttaranchal Ayurvedic College 
Address  Department of Swasthavritta and Yoga, Uttaranchal Ayurvedic College, 17, Old Mussoorie Rd, Kairwaan Gaon, Dehradun, Uttarakhand, India

Dehradun
UTTARANCHAL
248009
India 
Phone  8958153491  
Fax    
Email  yudhisharma1339@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Smita Zambare 
Designation  HOD 
Affiliation  Department of Swasthavritta and Yoga, Uttaranchal Ayurvedic College, 17, Old Mussoorie Rd, Kairwaan Gaon, Dehradun, Uttarakhand, India 
Address  Department of Swasthavritta and Yoga, Uttaranchal Ayurvedic College, 17, Old Mussoorie Rd, Kairwaan Gaon, Dehradun, Uttarakhand, India

Dehradun
UTTARANCHAL
248009
India 
Phone  8879133317  
Fax    
Email  smitazambare1@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Smita Zambare 
Designation  HOD 
Affiliation  Department of Swasthavritta and Yoga, Uttaranchal Ayurvedic College, 17, Old Mussoorie Rd, Kairwaan Gaon, Dehradun, Uttarakhand, India 
Address  Department of Swasthavritta and Yoga, Uttaranchal Ayurvedic College, 17, Old Mussoorie Rd, Kairwaan Gaon, Dehradun, Uttarakhand, India


UTTARANCHAL
248009
India 
Phone  8879133317  
Fax    
Email  smitazambare1@gmail.com  
 
Source of Monetary or Material Support  
Uttaranchal Ayurvedic College and Hospital,17, Old Mussoorie Rd, Kairwaan Gaon, Dehradun, Uttarakhand 248009, India 
 
Primary Sponsor  
Name  Yudhi Sharma 
Address  Uttaranchal Ayurvedic College, 17, Old Mussoorie Rd, Kairwaan Gaon, Dehradun, Uttarakhand 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 Yudhi  Uttaranchal Ayurvedic College,   Department of Swasthavritta and Yoga,Uttaranchal Ayurvedic College and Hospital, 17, Old Mussoorie Rd, Kairwaan Gaon, Dehradun, Uttarakhand 248009, India
Dehradun
UTTARANCHAL 
8958153491

yudhisharma1339@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethical Committee of Uttaranchal Ayurvedic College  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: AJIRNAM,  
 
Intervention / Comparator Agent  
snoIntervention/ComparatorTypeDrug-TypeProcedure NameDetails
1Intervention ArmDrugClassical(1) Medicine Name: Jeerak, Reference: Su. Su. 46/229, Route: Oral, Dosage Form: Dravaka, Dose: 1(g), Frequency: bd, Bhaishajya Kal: Pragbhakta, Duration: 2 Months, anupAna/sahapAna: Yes(details: -Ushna Jal), Additional Information: -Patients registered for the study will be provided 1 g roasted Jeerak seed packets. In the procedure, patients will be advised to chew the Jeerak seeds followed by lukewarm water orally. The drug will be administered to 50 patients over a period of 2 months. Patients will be instructed to follow up every 15 days during this period.
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  50.00 Year(s)
Gender  Both 
Details  1.Individuals having digestive problems.
2.Individuals who were fully cooperative for the study.
3.Individuals with informed consent to participate in the study. 
 
ExclusionCriteria 
Details  1.Individuals not willing for the trial.
2.Patients suffering from gastroesophageal reflux disease (GERD), peptic ulcers, irritable
bowel syndrome (IBS), Crohn’s disease, and ulcerative colitis.
3. Patients undergoing any abdominal surgical procedures.
4. Patients not addicted to tobacco, smoking and alcohol.
5. Individual who’s taking any medicine for digestion and acidity.
6. Individuals who take any medicine for digestion, constipation and acidity during this
study of 60 days. 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
To assess the combined effect of jeerak and pashchimottanasana in patients of ajeerna.  1. Baseline at day 1 before onset of treatment.

2. Follow up after every 15 days.

3. 2 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)   08/12/2025 
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="0"
Months="2"
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   Ajeerna is a digestive disorder that develops due to the improper digestion of food, leading to symptoms like anorexia, constipation, nausea. This clinical study aims to evaluate the combined effect of Jeerak and Pashchimottanasana practice in patients suffering from Ajeerna. Data will be collected at the baseline and after 2 months of intervention. Patients will be advised to follow up every 15 days during the 2-month study period for regular monitoring and assessment of clinical progress.  
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