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Clinical Trials/CTRI/2023/02/050050
CTRI/2023/02/050050CompletedNot Applicable

An Exploratory Approach for Validation and Standardization of Test Methods and Evaluators to Conduct In-Vivo Clinical Safety and Efficacy Testing of Hair Care Range of Products.

NovoBliss Research Private Limited1 site in 1 country40 target enrollmentStarted: February 28, 2023Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
40
Locations
1
Primary Endpoint
The objective of this validation study is to evaluate the standardize the methods, procedural steps, validate the hair growth rate measurement, 60-s combing test, pull test, pluck test, subjective scoring of Hair quality appearance and scalp condition - evaluations techniques that are used during the conduct of clinical safety and efficacy studies for hair care product evaluation at/by NovoBliss Research on healthy adult human subjects

Study Overview

Brief Summary

This is an In-house process validationstudy.

Thisvalidation study will be carried out on/by study staff of the NovoBlissResearch who is voluntarily wish to take part in this internal validationstudy. There are multiple hair evaluation techniques involved for testing hairgrowth products these testing methods for establishing documentary evidencedemonstrate that standardised procedural steps, processes and methods carriedout in testing for hair care safety and efficacy studies to maintain thedesired level of compliance.

It is veryimportant that in addition to final testing and compliance of products duringan actual clinical study, it is also assured that the processes willconsistently produce consistent results. The consistent results are establishedin terms of specifications for the outcome of the process.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18.00 Year(s) to 75.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Age: 18-75 years (both inclusive) at the time of consent.
  • Sex: Males and non-pregnant/non-lactating females (preferably equal number of males and females).
  • Females of childbearing potential must have a self-reported negative urine pregnancy.
  • Subject is in good general health as determined by the Investigator on the basis of medical history.
  • Subject is willing and able to follow and allow study staff to perform study test methods.
  • Subject is willing and able to follow the study directions, participate in the study, returning for all specified visits.
  • Subject must be able to understand and provide written informed consent to participate in the study.

Exclusion Criteria

  • Subject have history of allergy to any ink.
  • Subject have participated any clinical research study related to hair care products.
  • Subject having history of diabetes 4) Subject have history of mastectomy for cancer involving removal of lymph nodes within the past year, or treatment of any type of cancer within the last 6 months.
  • Subject having known history of any skin diseases including eczema, atopic dermatitis or active cancer.

Outcomes

Primary Outcomes

The objective of this validation study is to evaluate the standardize the methods, procedural steps, validate the hair growth rate measurement, 60-s combing test, pull test, pluck test, subjective scoring of Hair quality appearance and scalp condition - evaluations techniques that are used during the conduct of clinical safety and efficacy studies for hair care product evaluation at/by NovoBliss Research on healthy adult human subjects

Time Frame: Day 01 and Day 04

Secondary Outcomes

  • Not Applicable

Investigators

Sponsor Class
Contract research organization

Study Sites (1)

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