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Investigating the effectiveness of herbal cosmetic products (hair growth stimulating tonic, eyebrow growth stimulating tonic, hair growth stimulating shampoo, damaged hair revitalizing tonic, cream, face mask and soap) on hair growth and skin rejuvenation and introducing new formulations

Phase 3
Recruiting
Conditions
L81.4
Condition 1: Nonscarring hair loss. Condition 2: skin blemish.
Alopecia NOS
Other melanin hyperpigmentation
L65.9
Registration Number
IRCT20240402061400N2
Lead Sponsor
Razi University Vice president of Research and Technology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
420
Inclusion Criteria

Signing a written consent to participate in the study
Age between 18-70 years
In the categories of hair growth stimulating tonic and hair growth stimulating shampoo: patients must face at least one of the problems: hair loss, baldness or low density of hair.
In the category of eyebrow growth stimulating tonic: patients must face at least one of the following problems: eyebrow loss and low density of eyebrows.
In the category of hair regenerating tonic: patients must face the problem of damaged hair or hair with frizz.
In the categories of creams, masks and soaps: patients must have at least one of the following problems: skin spots, wrinkles on the skin, or darkening of the skin.

Exclusion Criteria

pregnancy
breastfeeding
History of using anabolic steroids in the last 6 months
History of using minoxidil 2% to 5% in the form of solution or foam or shampoo in the last 6 months
History of using finasteride and anti-androgen drugs in the last 6 months
History of taking drugs that cause hypertrichosis such as cyclosporine, systemic corticosteroids in the last 6 months
Suffering from chronic and acute kidney, liver, heart, vascular and pulmonary diseases

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hair density. Timepoint: At the beginning of the study (before the start of the intervention) and 7, 14, 21 and 28 days after the start of the study. Method of measurement: Digital image and view.;Patient satisfaction. Timepoint: 7, 14, 21 and 28 days after the start of the study. Method of measurement: questionnaire.;Hair regrowth based on doctor's opinion. Timepoint: 7, 14, 21 and 28 days after the start of the study. Method of measurement: Digital image and view.;Size and number of skin spots. Timepoint: At the beginning of the study (before the start of the intervention) and 7, 14, 21 and 28 days after the start of the study. Method of measurement: Digital image and view.
Secondary Outcome Measures
NameTimeMethod
Hair growthHeadache. Timepoint: At the beginning of the study (before the start of the intervention) and 7, 14, 21 and 28 days after the start of the study. Method of measurement: Ask the patient.;Itching. Timepoint: At the beginning of the study (before the start of the intervention) and 7, 14, 21 and 28 days after the start of the study. Method of measurement: Ask the patient.;Erythema-redness. Timepoint: At the beginning of the study (before the start of the intervention) and 7, 14, 21 and 28 days after the start of the study. Method of measurement: Ask the patient.
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