Assessment of the Effects and Tolerance of the RV4986A Lotion in Men With AGA After Hair Transplant

NCT ID: NCT06576492

Last Updated: 2024-08-28

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-07-05
• Study Completion Date: 2023-06-12

Brief Summary

Alopecia involves a diminution of visible hair that can have significant psychosocial effects and impairment of quality of life. There are numerous types of alopecia, among them, androgenic alopecia (AGA) is the most common form surgically treatable.

Androgenic alopecia is characterized by progressive visible thinning of scalp hair in genetically susceptible men (MAGA, or male pattern androgenic alopecia) and in some women (FPHL, or female pattern hair loss).

Among the plethora of products available proposed to promote hair growth in the scalp, only 2 medications are approved by the US Food and Drug Administration (FDA). These medications are finasteride (systemic) and minoxidil (topical).

In some cases, limited perceived efficacy of these treatments, poor tolerance, fear and lack of information on treatment duration and possible adverse events may lead to premature stop of treatment, disappointment and influence on patient compliance.

When conventional treatments have proven to be deceptive, a surgical treatment can be considered: hair transplant, that has evolved mainly with the aim of making the results look more and more natural.

Hair transplant, although performed on an outpatient basis, is an invasive technique, with the following immediate side effects: pain, pruritus, inflammation, scabs, swollen eyelids with tearing which last about 15 days. A social exclusion for 15 days after the transplant is generally necessary. For 1 to 2 months, the Red Scalp syndrome or inflammatory scalp is observed.

The growth of transplanted hair starts from the 6th month and the expected result is not really achieved until one year.

The product RV4986A is a non-rinsed cosmetic lotion intended to be used every day on the entire scalp especially in case of hormonal or hereditary chronic hair loss (as AGA) and also before hair transplant in order to prepare hair scalp and after hair transplant in order to soothe the scalp.

To date, no consensus and guidelines for pre- and post-transplant management exist regarding cosmetic products to apply that could limit their transplant side effects in time and intensity.

The aim of the study is to assess the effect of a new product (topical lotion) developed as an adjuvant product pre- and post-transplant that prepares hair scalp before the transplant and soothes it after hair transplant.

Conditions

Androgenic Alopecia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Treated group

Application of RV4986A lotion associated with RD0057H shampoo (Extra Doux shampoo)

Group Type: EXPERIMENTAL

RV4986A lotion

Intervention Type: OTHER

• Application between Month -0.5 and Month 0 (before hair transplant): once a day on the entire scalp
• From 4 days after hair transplant and until Visit 4 (Month 0,5 post transplant): once a day on the recipient area
• Between Month 0.5 and Month 12: once a day on the entire scalp

RD0057H shampoo

Intervention Type: OTHER

• Application between Month -0.5 and Month 0 (before hair transplant): at usual frequency when required on the entire scalp
• From 2nd day after hair transplant and until the 7th day after hair transplant: application on the recipient area with a spray containing mixture of water and shampoo. For the rest of the head application with the same modalities than before hair transplant
• From the 8th day after hair transplant to the 15th day: application with a sponge on the recipient area
• From the 16th day after hair transplant and for the next 12th months: application with the same modalities than before hair transplant

Control group

Application of RD0057H shampoo (Extra Doux shampoo)

Group Type: OTHER

RD0057H shampoo

Intervention Type: OTHER

• Application between Month -0.5 and Month 0 (before hair transplant): at usual frequency when required on the entire scalp
• From 2nd day after hair transplant and until the 7th day after hair transplant: application on the recipient area with a spray containing mixture of water and shampoo. For the rest of the head application with the same modalities than before hair transplant
• From the 8th day after hair transplant to the 15th day: application with a sponge on the recipient area
• From the 16th day after hair transplant and for the next 12th months: application with the same modalities than before hair transplant

Interventions

RV4986A lotion

• Application between Month -0.5 and Month 0 (before hair transplant): once a day on the entire scalp
• From 4 days after hair transplant and until Visit 4 (Month 0,5 post transplant): once a day on the recipient area
• Between Month 0.5 and Month 12: once a day on the entire scalp

Intervention Type: OTHER

RD0057H shampoo

• Application between Month -0.5 and Month 0 (before hair transplant): at usual frequency when required on the entire scalp
• From 2nd day after hair transplant and until the 7th day after hair transplant: application on the recipient area with a spray containing mixture of water and shampoo. For the rest of the head application with the same modalities than before hair transplant
• From the 8th day after hair transplant to the 15th day: application with a sponge on the recipient area
• From the 16th day after hair transplant and for the next 12th months: application with the same modalities than before hair transplant

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Male
• Subject requiring hair transplant with micrografts (strip technique or FUE technique)
• Subject aged ≥ 18 years old
• Subject having androgenetic alopecia selected by the investigator for a hair transplant

• Subject having any other hair disorder or hair disease (telogen effluvium, alopecia areata, cicatricial alopecia, hair shaft disorder, trichotillomania…) and liable to interfere with the study assessments
• Subject having dermatological pathology or evolutive skin lesion on the scalp (psoriasis, seborrheic dermatitis, severe erythema, severe excoriation, severe sunburn, …)
• Iron deficiency (confirmation by ferritin assay results from less than 3 months performed during preoperative assessment)
• Thyroid disorders (confirmation by thyroid hormon assay results from less than 3 months performed during preoperative assessment)
• Systemic treatment with antithyroid or iron supplement established or modified within 3 months before the inclusion or planned during the study
• Radiotherapy or chemotherapy at any time before the inclusion or planned during the study
• Systemic anti-hair loss treatment (anti-androgenic treatments…) established or modified within 6 months before the inclusion visit or planned during the study
• Topical anti-hair loss treatment (Minoxidil…) established or modified within 3 months before the inclusion visit or planned during the study
• Any other systemic treatment (cardiovascular, endocrine, antidepressant, antipsychotic, …) established or modified during the previous weeks before the inclusion or planned to be established or modified during the study, liable to interfere with the evaluation of the efficacy or cutaneous tolerance of the products according to the investigator's assessment
• Any other topical treatment or product applied on the scalp within previous weeks before the inclusion or planned during the study that can limit the effectiveness of the transplant and liable to interfere with the study assessments, according to the investigator's opinion

• Minimum Eligible Age: 18 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Pierre Fabre Dermo Cosmetique

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Instituto Medico Ricart

Madrid, Chamartin, Spain

Countries

Spain

Other Identifiers

RV4986A20200299

Identifier Type: -

Identifier Source: org_study_id