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CTRI Number  CTRI/2025/02/080561 [Registered on: 14/02/2025] Trial Registered Prospectively
Last Modified On: 10/10/2025
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Drug
Ayurveda
Other (Specify) [AYURVEDA]  
Study Design  Single Arm Study 
Public Title of Study   INTERVENTIONAL ROLE OF SWALP KHADIR VATIKA IN MOUTH ULCERS 
Scientific Title of Study   Pharmaceutico-Analytical Standarization of Swalp Khadir Vatika and its clinical evaluation in Mukhgatavrana with special reference to oral ulcers 
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. Sana Khan 
Designation  MD Scholar 
Affiliation  State Ayurvedic College and Hospital  
Address  State Ayurvedic College and Hospital ,Lucknow UP
Omaxe Sanskriti ,Arjunganj Lucknow
Lucknow
UTTAR PRADESH
226004
India 
Phone  8853984640  
Fax    
Email  sanakhandx@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr, Rajeev Narayan Bilas 
Designation  Reader -Post graduate Department of Rasa shastra and Bhaisajya kalpana  
Affiliation  State Ayurvedic College and Hospital  
Address  State Ayurvedic College and Hospital,Lucknow
State Ayurvedic College and Hospital,Lucknow
Lucknow
UTTAR PRADESH
226004
India 
Phone  8601447447  
Fax    
Email  RAJEEVBILAS427@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr. Sana Khan 
Designation  MD Scholar 
Affiliation  State Ayurvedic College and Hospital  
Address  State Ayurvedic College and Hospital,Lucknow ,UP
State Ayurvedic College and Hospital,Lucknow ,UP
Lucknow
UTTAR PRADESH
226003
India 
Phone  08853984640  
Fax    
Email  sanakhandx@gmail.com  
 
Source of Monetary or Material Support  
State Ayurvedic College and Hospital ,Lucknow - 226004 
 
Primary Sponsor  
Name  State Ayurvedic College and Hospital Lucknow  
Address  Turiyaganj,Old Haiderganj Lucknow- 226004 
Type of Sponsor  Government medical college 
 
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 Sana Khan   State Ayurvedic College and Hospital ,Lucknow   Department of Rasashastra and Bhaisajya Kalpana ,Lucknow ,UP
Lucknow
UTTAR PRADESH 
8853984640

sanakhandx@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
INSTITUTIONAL ETHICS COMMITEE  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition:K120||Recurrent oral aphthae. Ayurveda Condition: MUKHAROGAH,  
 
Intervention / Comparator Agent  
snoIntervention/ComparatorTypeDrug-TypeProcedure NameDetails
1Intervention ArmDrugClassical(1) Medicine Name: SWALPA KHADIR VATIKA , Reference: BHAISAJYA RATNAVALI , Route: Oral, Dosage Form: Gutika/Vati/Ghana Vati/ Tablets, Dose: 250(mg), Frequency: qid, Bhaishajya Kal: Abhakta, Duration: 4 Days, anupAna/sahapAna: No, Additional Information: -NIL
 
Inclusion Criteria  
Age From  16.00 Year(s)
Age To  60.00 Year(s)
Gender  Both 
Details  Focal site with size less than 1 CM , Patients presenting with minimum 3 classification signs and symptoms of Mukhgata vrana or Oral Ulcers  
 
ExclusionCriteria 
Details  HIV +ve or Immunecompromised patients ,Pregnant and lactating mothers, Chain smokers , Uncontrolled Diabetes melitus , Age below 16 years or above 60 years old . 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
CBC, Serum Creatinine
Viral Marker {If possible } 
Before trial ,2 weeks , 4 weeks  
 
Secondary Outcome  
Outcome  TimePoints 
CBC, Serum Creatinine   Before trial , 15 days ,After trial  
 
Target Sample Size   Total Sample Size="50"
Sample Size from India="50" 
Final Enrollment numbers achieved (Total)= "0"
Final Enrollment numbers achieved (India)="50" 
Phase of Trial   Phase 2 
Date of First Enrollment (India)   25/02/2025 
Date of Study Completion (India) 30/10/2025 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Date Missing 
Estimated Duration of Trial   Years="0"
Months="3"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Yet Recruiting 
Recruitment Status of Trial (India)  Completed 
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
Modification(s)  
THE PRESENT THESIS ENTITLED PHARMACEUTICO-ANALYTICAL STANDARIZATION OF SWALP KHADIR VATIKA AND ITS CLINICAL EVALUATION IN MUKHGATVRANA  WITH  SPECIAL REFERNECES TO ORAL ULCERS .

INTRODUCTION - 

SWALP KHADIR VATIKA is a polyherbal formulation described in Bhaishajya Ratnavali for mukhrog,danta,oshta,jhihwaa and taalugatrog.Same formulation is mentioned is mentioned in Vrindhmadhavkar and Vangasena . Due to its versatile therapeutics ,standarisation of Swalp Khadirvti is the need of the hour for maintaining its quality .The present dissertation work is the pioneer attempt of Pharmaceutical Analytical Standarization of Swalp Khadir vatika and its clinical evaluation its effect on Mukhgata vrana with special reference to Aphthous Ulcers .  CONTENTS OF SWALP KHADIR VAITAKA ARE 
1. KHADIR TWAK {ACAETIA CATECHU } 
2. JAVITRI {MYRISTICA FRAGNANS}
3. KARPOOR{ CINNAMOMUM CAMPHORA }
4. POOGPHALA { ARECA CATECHU }
5. KANKOL { PIPER CUBEBA } 


AIMS AND OBJECTIVE  

1. To validate ingredients of ‘SWALP KHADIR VATIKA ‘’ {Procurement of genuine raw material and its verification as per standard specification in mentioned under Pharmaceutical study.}

 2.To establish the SMP of “SWALP KHADIR VATIKA ”

 3.To standardize the final product “SWALP KHADIR VATIKA

.4.To establish analytical parameters of “SWALP KHADIR VATIKA 

5.To evaluate the clinical efficacy of the Swalp khadir Vatika in Mukhgat vrana with special reference to Aphthous ulcers 

 PLAN OF STUDY    
  1 .  CONCEPTUAL STUDY 
      A . LITERARY REVIEW 
      B . DRUG REVIEW  
2. PHARMACEUTICAL  STUDY 
   1. ANALYTICAL  STUDY 
      A . ORAGANOLEPTIC STUDY 
      B . PHYSICO-CHEMICAL STUDY 

3. CLINICAL STUDY 
   
SAMPLE SOURCE - IPD AND OPD OF STATE AYURVEDIC COLLEGE AND HOSPITAL , LUCKNOW  
AGE GROUP - 16-60 YEAR , SEX- MALE /FEMALE  

DOSE - 1 TABLETS FOUR TIMES DAILY ,EMPTY STOMACH , DO NOT SWALLOW ,INSTEAD SUCK IN MOUTH   { EACH TABLET WILL BE 250MG } 


DURATION OF STUDY WILL BE FOR 14 DAYS 

FOLLOW UP- FOLLOW UP OBSERVATIONS WILL BE CONTINUED FOR 14 DAYS AFTYER COMPLETION OF CLINICAL TRIAL  


 SAMPLE SIZE - 50 PATIENTS IN THE GROUP 

INCLUSION CRITERIA - AGE FROM 16-60 YEARS OF BOTH SEXES
                                              FOCAL SIZE LESS THAN 1 CM ,   
                                                  
PATIENTS WITH MINIMUM 3 CLASSICAL SIGN AND SYMPTOMS OF  MUKHGATA VRANA /ORAL ULCERS  


EXCLUSION CRITERIA -   PATIENTS BELOW 16 AND ABOVE 60 YEARS 
                                              IMMUNE COMPROMISED STATE , UNCONTROLLED DIABETES  


INVESTIGATIONS - CBC , LFT  , VIRAL MARKER { IF REQUIRED }, RBS ,HBA1C , {IF REQUIRED } 


CRITERIA FOR ASSESSMENT - 
THE OVERALL ASSESSMENT  AS STATED BELOW- 

1 . A PATIENT IN WHOM THERE WAS REDUCTION IN THE ASSESSMENT CRITERIA TO GRADE 0 AGAINTS THE INITIAL SEVERITY  SCORING IS CONSIDERED AS 91-100% . IT IS CONSIDERED AS GOOD  RESPONSE . 

PATIENT IN WHOM THERE WAS REDUCTION IN 2 LEVELES OF THE ASSEMENT CRITERIA AGAINTS THE INITIAL SEVERITY SCORING IS TAKEN AS 61-90 % RESPONSE . IT IS TAKEN AS MARKED RESPONSE .

3.PATIENTS IN WHOM THERE WAS REDUCTION IN ONE LEVEL OF THE ASSESSMENT CRITERIA AGAINST THE INITIAL SEVERITY IS TAKEN AS 31- 60 %  RESPONSE . 

4. PATIENTS IN WHOM ASSESSMENT CRITERIA REMAINED AGAINST THE INITIAL SEVERITY SCORING IS TAKEN AS 10-30% RESPONSE AND CONSIDERED AS POOR RESPONSE . 
 
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