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CTRI Number  CTRI/2013/09/003960 [Registered on: 05/09/2013] Trial Registered Retrospectively
Last Modified On: 15/07/2013
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Other (Specify) [Cosmetics]  
Study Design  Other 
Public Title of Study   To check irritation potential of the given samples (Patch test) 
Scientific Title of Study   SINGLE APPLICATION CLOSED PATCH TEST TO EVALUATE THE SAFETY OF SKIN CARE FORMULATIONS ON HEALTHY HUMAN SUBJECTS REPRESENTING VARIED SKIN TYPES. 
Trial Acronym  PIPT 
Secondary IDs if Any  
Secondary ID  Identifier 
SRC/CD/408, Version: 01, Dated: May 18, 2013  Protocol Number 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Ms Uma Ayachit 
Designation  Scientist 
Affiliation  KETs Scientific Research Centre  
Address  The KET’s, Scientific Research Centre,Cosmetology Division, 4th Floor,V. G. Vaze College Campus,Mulund(E),Mumbai

Mumbai (Suburban)
MAHARASHTRA
400081
India 
Phone  02225639644  
Fax  02221635404  
Email  uma@kelkarcosmetology.com  
 
Details of Contact Person
Scientific Query
 
Name  Ms Uma Ayachit 
Designation  Scientist 
Affiliation   
Address  The KET’s, Scientific Research Centre,Cosmetology Division, 4th Floor,V. G. Vaze College Campus,Mulund(E),Mumbai


MAHARASHTRA
400081
India 
Phone  02225639644  
Fax  02221635404  
Email  uma@kelkarcosmetology.com  
 
Details of Contact Person
Public Query
 
Name  Ms Uma Ayachit 
Designation  Scientist 
Affiliation   
Address  The KET’s, Scientific Research Centre,Cosmetology Division, 4th Floor,V. G. Vaze College Campus,Mulund(E),Mumbai


MAHARASHTRA
400081
India 
Phone  02225639644  
Fax  02221635404  
Email  uma@kelkarcosmetology.com  
 
Source of Monetary or Material Support  
ITC Ltd,Peenya Industrial Area, Peenya, Bangalore - 560058. Tel: 080 216303911  
 
Primary Sponsor  
Name  ITC Limited Peenya Industrial Area Peenya Bangalore 
Address  ITC Life Sciences and Technology CENTRE No. 3, 1st Main Road, Peenya Industrial Area, 1st phase.Bangalore - 560058. Tel: 080 216303911.  
Type of Sponsor  Research institution 
 
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 
Ms Uma Ayachit  KETs Scientific Research Centre   KETs Scientific Research Centre.V.G.Vaze College campus,Mithaghar Road, Mulund(E)Mumbai (Suburban)
Mumbai (Suburban)
MAHARASHTRA 
02225639644
02221635404
uma@kelkarcosmetology.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
The Institutional Scientific and Ethics Committee, Affiliated to KETs Scientific Research Centre  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  skin patch test  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Cream M#55/75  Day 1 (day of patch application), Day 2 (0 hrs. of Patch Removal i.e. 24 hrs. of patch application), Day 3 (24 hrs. of patch removal) and Day 9 (1 week after patch removal). 
Intervention  Cream MADC-SFA-204  Day 1 (day of patch application), Day 2 (0 hrs. of Patch Removal i.e. 24 hrs. of patch application), Day 3 (24 hrs. of patch removal) and Day 9 (1 week after patch removal). 
Intervention  Face Wash FW 133  Day 1 (day of patch application), Day 2 (0 hrs. of Patch Removal i.e. 24 hrs. of patch application), Day 3 (24 hrs. of patch removal) and Day 9 (1 week after patch removal).  
Intervention  Shower Gel TSP 69-087B  Day 1 (day of patch application), Day 2 (0 hrs. of Patch Removal i.e. 24 hrs. of patch application), Day 3 (24 hrs. of patch removal) and Day 9 (1 week after patch removal). 
Intervention  Shower Gel TSP 69-088B  Day 1 (day of patch application), Day 2 (0 hrs. of Patch Removal i.e. 24 hrs. of patch application), Day 3 (24 hrs. of patch removal) and Day 9 (1 week after patch removal). 
Intervention  Shower Gel TSP 69-088C  Day 1 (day of patch application), Day 2 (0 hrs. of Patch Removal i.e. 24 hrs. of patch application), Day 3 (24 hrs. of patch removal) and Day 9 (1 week after patch removal). 
Comparator Agent  Sodium Lauryl Sulphate 3% Solution   Day 1 (day of patch application), Day 2 (0 hrs. of Patch Removal i.e. 24 hrs. of patch application), Day 3 (24 hrs. of patch removal) and Day 9 (1 week after patch removal).  
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  50.00 Year(s)
Gender  Both 
Details  1.Volunteer (female/ male) in generally good health.
2.Volunteer between the ages of 18 and 50 years.
3.Volunteer has not participated in a similar clinical investigation in the past four weeks.
4.Volunteer willing to give a written informed consent and come for regular observation. 
 
ExclusionCriteria 
Details  1.A known history or present condition of allergic response to any cosmetic products.
2.Skin disease (e.g. psoriasis, atopic dermatitis or other cutaneous manifestations on the scalp), which would interfere with the test readings.
3.Medications (e.g. steroids or antihistamines), which would compromise the study.
4.Pregnant or lactating females. 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Case Record Numbers 
Blinding/Masking   Participant Blinded 
Primary Outcome  
Outcome  TimePoints 
irritation potential  first observation will be made at 30 minutes of patch removal (0 hr. observation). The further observations will be at 24 hrs and 1 week of patch removal.  
 
Secondary Outcome  
Outcome  TimePoints 
investigational products to be tested for irritancy test  On each subject’s back one patch of each investigational product will be applied on Day 1. This will be 9 days study. For all the products and positive control the subjects will be assessed by the study dermatologist on Day 1 (Day of patch application), Day 2 (0 hrs. of patch removal i.e. 24 hrs. of patch application), Day 3 (24 hrs. of patch removal) and Day 9 (1 week after patch removal).  
 
Target Sample Size   Total Sample Size="24"
Sample Size from India="24" 
Final Enrollment numbers achieved (Total)= ""
Final Enrollment numbers achieved (India)="" 
Phase of Trial   Phase 2 
Date of First Enrollment (India)   30/05/2013 
Date of Study Completion (India) Date Missing 
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)   Not Applicable 
Recruitment Status of Trial (India)  Completed 
Publication Details    
Individual Participant Data (IPD) Sharing Statement

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

Brief Summary  

Skin Irritation Test:

Irritants are substances that damage the skin. The damage will depend upon the nature, concentration and duration of exposure. Irritation is manifested as inflammatory responses such as erythema (redness), Oedema (swelling), and vesiculation and finally to an intense suppurate reaction without the involvement of the immune system. The irritation potential of a substance can be assessed by human patch test.

 
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