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CTRI Number  CTRI/2017/01/007641 [Registered on: 06/01/2017] Trial Registered Retrospectively
Last Modified On: 13/01/2022
Post Graduate Thesis  No 
Type of Trial  Observational 
Type of Study
Modification(s)  
Safety 
Study Design  Other 
Public Title of Study   safety of Investigational products by assessing the irritation after patch application on healthy human volunteers.  
Scientific Title of Study   Evaluation of dermatological safety of investigational products by primary irritation patch test on healthy human volunteers of varied skin types 
Trial Acronym  not applicable 
Secondary IDs if Any  
Secondary ID  Identifier 
01/067/16 V01 12092016  Protocol Number 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Siddheshwar Mathpati 
Designation  Investigator  
Affiliation  MASCOT-SPINCONTROL India Pvt. Ltd. 
Address  MASCOT-SPINCONTROL India Pvt. Ltd. Unit 2, Neeru Silk Mills, Mathuradas Mill compound, N.M. Joshi Marg - Lower Parel, Mumbai – 400013, INDIA
MASCOT-SPINCONTROL India Pvt. Ltd. Unit 2, Neeru Silk Mills, Mathuradas Mill compound, N.M. Joshi Marg - Lower Parel, Mumbai – 400013, INDIA
Mumbai
MAHARASHTRA
400013
India 
Phone  2243349191  
Fax  2243349191  
Email  siddheshwar@mascotspincontrol.in  
 
Details of Contact Person
Scientific Query
 
Name  Mr Mohit Lalvani 
Designation  Study Director 
Affiliation  MASCOT-SPINCONTROL India Pvt. Ltd. 
Address  MASCOT-SPINCONTROL India Pvt. Ltd. Unit 2, Neeru Silk Mills, Mathuradas Mill compound, N.M. Joshi Marg - Lower Parel, Mumbai – 400013, INDIA

Mumbai
MAHARASHTRA
400013
India 
Phone  2243349191  
Fax    
Email  mohit@mascotspincontrol.in  
 
Details of Contact Person
Public Query
 
Name  Mr Mohit Lalvani 
Designation  Study Director 
Affiliation  MASCOT-SPINCONTROL India Pvt. Ltd. 
Address  MASCOT-SPINCONTROL India Pvt. Ltd. Unit 2, Neeru Silk Mills, Mathuradas Mill compound, N.M. Joshi Marg - Lower Parel, Mumbai – 400013, INDIA

Mumbai
MAHARASHTRA
400013
India 
Phone  2243349191  
Fax    
Email  mohit@mascotspincontrol.in  
 
Source of Monetary or Material Support  
not applicable  
 
Primary Sponsor  
Name  ITC LIMITED ITC Life Sciences and Technology Centre 
Address  ITC Life Sciences and Technology Centre, No. 3, 1st Main Road, Peenya Industrial Area, I Phase Peenya, Bangalore – 560058, INDIA 
Type of Sponsor  Other [Multinational] 
 
Details of Secondary Sponsor  
Name  Address 
not applicable  not applicable 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Siddheshwar Mathpati  MASCOT-SPINCONTROL India Pvt. Ltd.  MASCOT-SPINCONTROL India Pvt. Ltd. Unit 2, Neeru Silk Mills, Mathuradas Mill compound, N.M. Joshi Marg - Lower Parel, Mumbai – 400013, INDIA
Mumbai
MAHARASHTRA 
2243349191

siddheshwar@mascotspincontrol.in 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Ethos- An Institutional Ethics committee (Mumbai)  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  healthy  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  1.1. Soap(TSP 110- 186C) 2. Soap (TSP 110-109) 3. Soap (TSP 110-140) 4. Soap (TSP 110-151) 5. Soap (TSP 111-013) 6. Soap (TSP 111-022) 7. Rinse – off (62-05) 8. Rinse – off (64-006) 9. Talc (124052) 10. Talc (039161)  1. Soap(TSP 110- 186C) 2. Soap (TSP 110-109) 3. Soap (TSP 110-140) 4. Soap (TSP 110-151) 5. Soap (TSP 111-013) 6. Soap (TSP 111-022) 7. Rinse – off (62-05) 8. Rinse – off (64-006) 9. Talc (124052) 10. Talc (039161) 1. For products 01 to 08 the products are diluted 8% and solution are dispensed in the aluminum chambers of the patch and applied on the back of the volunteers at T0 visit. 2. For products 09 & 010; the product is talc product, 1:1 slurry are dispensed in the aluminum chambers of the patch and applied on the back of the volunteers at T0 visit.  
Comparator Agent  Sodium Lauryl Sulphate (SLS)   3% Solution 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  50.00 Year(s)
Gender  Both 
Details  Details Skin is healthy on the studied anatomic unit (free of eczema, wounds, inflammatory scar….)
Subjects representing varied skin types (ideally equal representation of all 4 skin types – Oily, Normal, Dry and combination) Subjects willing to come for regular follow up and ready to follow instructions during the study period
 
 
ExclusionCriteria 
Details  For female : Being pregnant or breastfeeding or having stopped to breastfeed in the past three months, Having refused to give his/her assent by signing the consent form, Taking part in another study liable to interfere with this study Being diabetic, Being asthmatic, Having eczema, oriasis, lichen plan, vitiligo whatever the considered area, Having disorder of the healing
(whatever the considered area),Having a rhinitis, allergic conjunctivitis or rhinosinusitis
 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
To evaluate the dermatological safety of
investigational products by primary irritation
patch test on healthy human volunteers of varied
skin types
 
t0 t1 t2 t8
 
 
Secondary Outcome  
Outcome  TimePoints 
not applicable  not applicabe 
 
Target Sample Size   Total Sample Size="24"
Sample Size from India="24" 
Final Enrollment numbers achieved (Total)= "23"
Final Enrollment numbers achieved (India)="23" 
Phase of Trial   N/A 
Date of First Enrollment (India)   09/09/2016 
Date of Study Completion (India) 22/09/2016 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Date Missing 
Estimated Duration of Trial   Years="0"
Months="0"
Days="9" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Completed 
Publication Details   not aplicable  
Individual Participant Data (IPD) Sharing Statement

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

Response - NO
Brief Summary  
Single Application, Closed Patch Test is conducted to measure the irritation potential of cosmetic products on the skin.
Objective: To evaluate the dermatological safety of investigational products by primary irritation patch test on healthy human volunteers of varied skin types.
Duration of study: 8 days study
Kinetics: T0 (Evaluation of test sites by Dermat and Subject, 
Patch application), T on evaporation of products, T+30mins post patch application, T1(Patch removal, Evaluation of test sites by Dermat and Subject post 30 minutes of patch removal), T2(Evaluation of test sites by Dermat and Subject post 24 hrs of  patch removal), T8 (Evaluation of test sites by Dermat and Subject post 1 week of patch removal and tracking the positive cases)
Population 24 healthy subjects(12 males + 12 females) The subjects are selected on the
basis of skin types:
3 males + 3 females for dry skin
3 males + 3 females for oily skin
3 males + 3 females for combination skin
3 males + 3 females for normal skin
Products: Soap(TSP-110-186C), Soap(TSP-110-109), Soap(TSP-110-140), Soap(TSP-110-151), Soap(TSP-111-013), Soap(TSP-111-022), Rinse –off (62-05), Rinse off (64-006), Hair leave – on (22002F1), Hair Leave – on (22002F2).
Positive control: 3% SLS
The test area is checked for erythema and oedema caused due to the products and
compared with positive control

 
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