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study to check hair removing capacity of hair depilator wipes

To evaluate the safety and efficacy of hair wipe with kopcolate through open label randomized study for the removal of hair in both male and female volunteers - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070418
Enrollment
24
Registered
2024-07-10
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Hair depilator wipe with active ingredient Potassium Thioglycollate 43%: Hair remover wipe with potassium thioglycolate 43% is applied and gently patted with a plastic spatula to make i

Sponsors

KOP Research Centre Private Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Female and male subjects with unwanted hair on arms and legs 2.Subjects aged between 18- 50 years of age 3.Subjects who are willing to sign informed concerned form. 4.Subjects consenting for photograph

Exclusion criteria

Exclusion criteria: 1.Subjects who doesn’t have hair or very scarce hair over arms and legs 2.Subjects below 18 years of age 3.Subjects who refuse to sign informed consent form 4.Pregnant and feeding women 5.Subjects who have wound at the application sites 6.Subjects with known allergy to any ingredient 7.Subjects with tattoo mark at area of application 8.Subjects under any medication.

Design outcomes

Primary

MeasureTime frame
To evaluate amount of hair removed, smoothness of skin, easy of application after using wipe for duration of 5 min, 7 min and 10 minutes. Assessment of efficacy are through questionnaire and photograph 1. Easy of application 2. Skin softness after hair removal 3. Satisfaction with the amount of hair removal. 4. odour of the product 5. Ease of removal after application All parameters assessed on scale of 0 to 5 Photo comparison for amount of hair removed before and after application.Timepoint: Duration of application is 5 min, 7 min and 10 minutes. No repeat application. Total duration 25 minutes only per subject.

Secondary

MeasureTime frame
To evaluate safety of IP after pre-decided duration of applicationTimepoint: 5 minutes 7 minutes and 10 minutes

Countries

India

Contacts

Public ContactDr Lakshmipathy R N

Smartmed Research Pvt Ltd

drinvestigator@myyahoo.com09538207347

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026