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CTRI Number  CTRI/2024/11/076242 [Registered on: 04/11/2024] Trial Registered Prospectively
Last Modified On: 10/03/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Drug
Ayurveda
Diagnostic 
Study Design  Randomized, Parallel Group, Multiple Arm Trial 
Public Title of Study   To Compare the effect of Varuna leaves paste With Ghee after the cow dung massage, Varuna leaves Siddha Ghee and also its Comparision with Manjistha Ghee in the management of Strech marks 
Scientific Title of Study   Evaluation of comparative efficacy of external application of Varuna Crataeva nurvala Buch Ham patra Kalka with Ghrita after the Gomaya Gharshana Varuna Patra Siddha Ghrita and Manjistha Ghrita in the management of Striae Gravidarum Kikkisa Three arm study  
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 Pallavi Dewangan 
Designation  PG Scholar 
Affiliation  Mahatma Gandhi Ayurved College Hospital and Research Centre Salod Wardha 
Address  Department of Dravyaguna Vigyan Datta Meghe Institute of Higher Education and Research Centre Mahatma Gandhi Ayurved College Salod Wardha 442001

Wardha
MAHARASHTRA
442001
India 
Phone  7691928631  
Fax    
Email  pallucph@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Jaimala Jadhav 
Designation  Professor 
Affiliation  Mahatma Gandhi Ayurved College Hospital and Research Centre Salod Wardha 
Address  Department of Dravyaguna Vigyan Datta Meghe Institute of Higher Education and Research Centre Mahatma Gandhi Ayurved College Salod Wardha 442001

Wardha
MAHARASHTRA
442001
India 
Phone  9922190843  
Fax    
Email  jaymalajadhav0610@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Jaimala Jadhav 
Designation  Professor 
Affiliation  Mahatma Gandhi Ayurved College Hospital and Research Centre Salod Wardha 
Address  Department of Dravyaguna Vigyan Datta Meghe Institute of Higher Education and Research Centre Mahatma Gandhi Ayurved College Salod Wardha 442001

Wardha
MAHARASHTRA
442001
India 
Phone  9922190843  
Fax    
Email  jaymalajadhav0610@gmail.com  
 
Source of Monetary or Material Support  
Mahatma Gandhi Ayurved College Hospital and Research Centre Salod Hirapur Wardha (Maharashtra) 442001 
 
Primary Sponsor  
Name  Mahatma Gandhi Ayurved College Hospital and Research Centre Salod Wardha 
Address  Department of Dravyaguna Vigyan Datta Meghe Institute of higher education and research centre Mahatma Gandhi Ayurved College Salod Wardha 442001 
Type of Sponsor  Research institution and hospital 
 
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 Pallavi Dewangan  Mahatma Gandhi Ayurved College   Department of kaychikitsa and strirog OPD in Mahatma Gandhi Ayurved College Salod Wardha 442001
Wardha
MAHARASHTRA 
7691928631

pallucph@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Mahatma Gandhi Ayurved College Hospital and Research Centre Institutional Ethics Committee Salod Wardha  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition:L99||Other disorders of skin and subcutaneous tissue in diseases classified elsewhere. Ayurveda Condition: KIKKISA-GARBINIROGAH,  
 
Intervention / Comparator Agent  
snoIntervention/ComparatorTypeDrug-TypeProcedure NameDetails
1Intervention ArmDrugClassical(1) Medicine Name: Varuna Patra, Reference: Bhaishajay ratnavali, Route: Topical, Dosage Form: Lepa Churna, Dose: 0(NA), Frequency: bd, Bhaishajya Kal: Adhobhakta, Duration: 8 Weeks, anupAna/sahapAna: No, Additional Information: this is a three arm study first group will be having 20 patient with intervention of Varuna Patra
2Comparator ArmDrugClassical(1) Medicine Name: Manjistha Ghrita, Reference: Charak Samhita, Route: Topical, Dosage Form: Ghrita, Dose: 0(NA), Frequency: bd, Bhaishajya Kal: Adhobhakta, Duration: 8 Weeks, anupAna/sahapAna: No, Additional Information: this is a three arm study the comparator group contain Manjistha Ghrita with 20 patient. all the three groups run parallel for 8 weeks
3Intervention ArmDrugClassical(1) Medicine Name: Varuna patra siddha Ghrita, Reference: bhaishajay ratnavali, Route: Topical, Dosage Form: Ghrita, Dose: 0(NA), Frequency: bd, Bhaishajya Kal: Adhobhakta, Duration: 8 Weeks, anupAna/sahapAna: No, Additional Information: this is a three arm study second group will be having 20 patient with intervention of Varuna Patra Siddha Ghrita
 
Inclusion Criteria  
Age From  25.00 Year(s)
Age To  45.00 Year(s)
Gender  Female 
Details  1. Female patient willing to participate with written informed consent.
2. Age group between 25-45 years.
3. 2 years history of last delivery.
4. no prior treatment for Kikkisa before 1 month. 
 
ExclusionCriteria 
Details  1. pregnant women
2. Lactating women
3. Any type of skin disease other than Kikkisa.
4. Patient having chronic disease eg. tuberculosis, jaundice etc.
5. Any malignancy on the affected part was excluded. 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   On-site computer system 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
To eliminate the Striae Gravidarum (Kikkisa) in Garbhani rog.  8 weeks 
 
Secondary Outcome  
Outcome  TimePoints 
To assess the efficacy of Varuna Patra Kalka with Ghrita after the Gomaya Gharshana, Varuna Patra siddha Ghrita and Manjistha Ghrita in management of Garbhani rog(Kikkisa)  8 weeks 
 
Target Sample Size   Total Sample Size="60"
Sample Size from India="60" 
Final Enrollment numbers achieved (Total)= "60"
Final Enrollment numbers achieved (India)="60" 
Phase of Trial   Phase 3/ Phase 4 
Date of First Enrollment (India)   24/11/2024 
Date of Study Completion (India) 09/03/2026 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) 09/03/2026 
Estimated Duration of Trial   Years="2"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Completed 
Recruitment Status of Trial (India)  Completed 
Publication Details
Modification(s)  
protocol published 
Individual Participant Data (IPD) Sharing Statement

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

Response - NO
Brief Summary
Modification(s)  
the volunteers will be informed about the study protocol. Willing participants will be randomly
selected as per computer generated table. Clinical research format will be prepared and validated.
Prior to the study approval will be taken from IEC, MGACHRC, Salod (H) Wardha and CTRI
registration will be done. After selection, each participant will be tested individually and selected
according to selection criteria. They are divided into three groups the trial is a Randomized parallel
arm Clinical Trial. it will include 8 weeks treatment period and follow up.
 
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