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CTRI Number  CTRI/2018/11/016288 [Registered on: 08/11/2018] Trial Registered Prospectively
Last Modified On: 27/04/2023
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Other (Specify) [N/AP]  
Study Design  Other 
Public Title of Study   Safety assessment of products on skin 
Scientific Title of Study   Evaluation of irritation potential of Skin Care Formulations on healthy human subjects. 
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
D01-6Q13-TE-OR18; Version: 01; Dated: 23/10/2018  Protocol Number 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Raji Patil 
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

Mumbai (Suburban)
MAHARASHTRA
400013
India 
Phone  022-43349191  
Fax    
Email  raji@mascotspincontrol.in  
 
Details of Contact Person
Scientific Query
 
Name  Dr Raji Patil 
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

Mumbai (Suburban)
MAHARASHTRA
400013
India 
Phone  022-43349191  
Fax    
Email  raji@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 (Suburban)
MAHARASHTRA
400013
India 
Phone  022-43349191  
Fax    
Email  mohit@mascotspincontrol.in  
 
Source of Monetary or Material Support  
Not Applicable 
 
Primary Sponsor  
Name  TTK Healthcare Limited 
Address  Protective Devices Division, Research and Development No. 3, Thirunerrmalai Road, Chrompet, Chennai-600044, Tamil Nadu, India 
Type of Sponsor  Other [FMCG] 
 
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 Raji Patil  Mascot-Spincontrol India Pvt. Ltd.  Unit 2, Neeru Silk Mills, Mathuradas Mill compound, N.M. Joshi Marg - Lower Parel, Mumbai – 400013, INDIA
Mumbai (Suburban)
MAHARASHTRA 
022-43349191

raji@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  Not Applicable 
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Deodorant Brand Name: SKORE(SD-002) Deodorant Brand Name: SKORE(SD-006) Deodorant Brand Name: SKORE(SD-007) Deodorant Brand Name: SKORE(SD-008) Deodorant Brand Name: SKORE(SD-009) Pocket Perfume Brand Name: SKORE(SPP-001) Pocket Perfume Brand Name: SKORE(SPP-002) Orgasmic Gel Brand Name: SKORE OH! (SOG-17)  1. For Products 1 to 7, the products are aerosol product. So it is applied by semi-occlusive method. The product is dispensed directly on the skin on the back of volunteer and it is occluded by the patch after it gets evaporated at T0 visit. 2. For product 8, The product are directly dispensed in the aluminium finn chambers of the patch and applied on the back of the volunteers at T0 visit 
Comparator Agent  Sodium Lauryl Sulphate (SLS) 3% Solution Negative Control (Distilled Water)  Not Applicable 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  60.00 Year(s)
Gender  Both 
Details  Skin is healthy on the studied anatomic unit (free of eczema, wounds, inflammatory scar….)
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   Open Label 
Primary Outcome  
Outcome  TimePoints 
To evaluate the irritation potential on healthy human subjects of Skin Care Formulations.  T0 (Evaluation of test sites by Dermatologist and Subject,
Patch application)
T1(Patch removal, Evaluation of test sites by Dermatologist, T2(Evaluation of test sites by Dermatologist and Subject post 24 hrs of patch removal)
T8 (Evaluation of test sites by Dermatologist and Subject post 1 week of patch removal and tracking the positive cases).
Formulations. 
 
Secondary Outcome  
Outcome  TimePoints 
Not Applicable  Not Applicable 
 
Target Sample Size   Total Sample Size="24"
Sample Size from India="24" 
Final Enrollment numbers achieved (Total)= "24"
Final Enrollment numbers achieved (India)="24" 
Phase of Trial   N/A 
Date of First Enrollment (India)   08/11/2018 
Date of Study Completion (India) 22/11/2018 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Date Missing 
Estimated Duration of Trial   Years="0"
Months="0"
Days="8" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Completed 
Publication Details   Not Applicable 
Individual Participant Data (IPD) Sharing Statement

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

Brief Summary  

Single Application, semi occlusive, Closed Patch Test is conducted to measure the irritation potential of cosmetic products on the skin.

Objective: To evaluate the  irritation potential on healthy human subjects of Skin Care Formulations.

Duration of study: 8 days study

Kinetics: T0 (Evaluation of test sites by Dermat and Subject,

                      Patch application)

                  T1(Patch removal, Evaluation of test sites by Dermat

                 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)

Products :  Deodorant Brand Name: SKORE(SD-002), Deodorant Brand Name: SKORE(SD-006), Deodorant Brand Name: SKORE(SD-007), Deodorant Brand Name: SKORE(SD-008), Deodorant Brand Name: SKORE(SD-009), Pocket Perfume Brand Name: SKORE(SPP-001), Pocket Perfume Brand Name: SKORE(SPP-002), Orgasmic Gel

Brand Name: SKORE OH! (SOG-17)

 Positive control : 3% SLS

Negative Control :Distilled Water 

The test area is checked for erythema and oedema caused due to the products and compared with positive control.

 
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