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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04489576
Other study ID # Sohagu310
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 15, 2020
Est. completion date June 2021

Study information

Verified date January 2021
Source Sohag University
Contact Amr Abdelhamed, MD
Phone +201005825574
Email dramr80@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Hair appearance is an important issue for females. Treatment of hair with keratin has been popular among females nowadays. Although chemical hair straightening application has a beneficial effect on hair shafts with the repair of the broken cuticle, some side effects may occur. Therefore, this study aims to study the efficacy and safety of such new non-formaldehyde widely used keratin treatments on hair by assessment of changes of the scalp, hair density, and the morphology, color, and ultrastructure of hair shaft after application.


Description:

Hair is an important feature for most women that contribute to one's individual identity. The appearance and morphology of the hair is one of the divergent traits in humans. Keratin in hair care products has two effects; it can penetrate the cortex of the hair fiber improving the mechanical properties of damaged fibers and promotes a surface coating that prevents or decreases water diffusion through the hair fibers.These properties have beneficial effects on the hair structure replacing lost keratin.However, the side effects and safety of this treatment have not yet been completely evaluated.There are many different brands of the keratin hair treatment, all with nearly the same basic chemical composition. Non-formaldehyde containing keratin straightening products, also known as safe keratin treatments (SKT) have recently been introduced to the market.Therefore, this study aims to study the efficacy and safety of such new non formaldehyde widely used keratin treatments on hair.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date June 2021
Est. primary completion date April 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria: - The study will include female patients aged between 18 and 55 years, with hair curl types from III to V according to L'Oréal Curl Classification. The Patients will be randomized by simple randomization into 3 groups, 10 patients for each. Exclusion Criteria: - Pregnant and lactating women. - Patients having hair loss or under treatment of hair loss in last 3 months. - Patients with previous history of keratin treatment. - Patients with scalp affection including infection, injury or surgery - Patients with chronic medical diseases. - Patients with anemia (hemoglobin level <10mg/dl) or under its treatment.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Keratin hair treatment (Keratin Cure ®) versus (QOD Max ®)
Hair will be treated with 2 different types of keratin in groups 1 & 2. All steps of keratin application will be done in group 3 without keratin application as a control group.

Locations

Country Name City State
Egypt Sohag University Sohag

Sponsors (1)

Lead Sponsor Collaborator
Sohag University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of hair shedding using the Visual analogue scale (VAS) It will be used to evaluate hair shedding. Hair shedding is scored on a scale of 1-6. Women are asked to look at the scale and point to the photograph that best correlates with the amount of hair shed on an average day. Grades 1-3 are considered normal. Grade 4 is borderline, while Grades 5 and 6 indicate excessive shedding. Baseline, 2 months, 4 months, 6 months
Primary Change of hair morphology using trichoscope It will be used to evaluate hair structure and scalp. Hair density/cm 2 and thickness (mm) will be measured in the frontal, temporal and vertex areas in all participants. Baseline, 2 months, 4 months, 6 months
Primary Change of hair morphology using Transmission Electron Microscopic examination Randomly selected samples of each group will be fixed in 3% glutaraldehyde for over a period of 4 hours at 4°C and processed to be examined by transmission electron microscope Baseline, 2 months, 4 months, 6 months
Primary Safety evaluation to detect any side effects that will be reported either by the patient or by the physician. at 6 months
Secondary Change of patient satisfaction questionnaire about keratin treatment A 5 items Questionnaire will be completed by the patients to evaluate their satisfaction about the treatment. The questionnaire consists of Q1 (1-5), Q2,3 (1-7), Q4 (1-4) and Q5 has 3 sub-items Q5a, Q5b, Q5c (1-5 for each). Total score ranges from 7-38. Higher scores are associated with higher dissatisfaction. Baseline, 2 months, 4 months, 6 months
See also
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