XVIE for Alopecia

Enrolling by invitation at 1 trial location
DC
Overseen ByDr. Chesahna Kindred, MD, FAAD
Age: 18+
Sex: Female
Trial Phase: Academic
Sponsor: Restore Biologics Holdings, Inc. dba Xtressé
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to test a new treatment, XVIE, to determine if it can safely and effectively boost hair growth in women experiencing thinning hair. The study will track changes in hair quality, volume, and thickness using photos and gather feedback on participants' satisfaction with the results and application process. Women who have noticed thinning hair and meet specific criteria can participate. Participants will receive the treatment, applied to their scalp with tiny needles, twice over four months. As an unphased trial, this study offers participants the opportunity to potentially benefit from a novel treatment while contributing to valuable research.

Do I need to stop taking my current medications for the trial?

The trial information does not specify if you need to stop taking your current medications. However, if you've recently changed hair treatments, you may not be eligible.

What prior data suggests that the XVIE microneedling process is safe for improving hair growth?

Research shows that using the XVIE solution on the scalp is generally safe. Made from human amniotic fluid, this solution has been studied for its potential to boost hair growth. In earlier studies, researchers applied it with microneedling, a method involving tiny needle pricks, and found it to be safe with few side effects.

While the quality of data on microneedling can vary, some studies have shown it can aid hair growth without major side effects. Most participants in these studies did not experience serious problems. Although the safety of XVIE has been studied, further research could provide clearer results. However, current evidence suggests it is safe for use in hair growth treatments.12345

Why are researchers excited about this trial?

Unlike standard treatments for alopecia, which often include topical minoxidil or oral finasteride, XVIE is a unique approach that uses a microneedling process to apply a human amniotic fluid-derived product directly to the scalp. This treatment is rich in bioreactive molecules like growth factors, cytokines, and hyaluronic acid, which are believed to promote hair growth by regenerating and repairing scalp tissues. Researchers are excited about XVIE because it leverages these advanced biological components to potentially offer a more effective and regenerative treatment option for hair loss.

What evidence suggests that XVIE might be an effective treatment for alopecia?

Research has shown that microneedling can aid hair growth. Studies have found it to be a safe and promising method for both men and women experiencing hair loss. This trial will evaluate the effectiveness of the XVIE microneedling process, which involves creating tiny holes in the scalp to enhance treatment efficacy. XVIE contains active ingredients, such as growth factors and proteins, that promote hair growth. While microneedling alone has shown potential, combining it with XVIE might further improve results.13467

Who Is on the Research Team?

MY

Melissa Y Rayner, MS

Principal Investigator

Restore Biologics Holding, Inc dba Xtressé

Are You a Good Fit for This Trial?

This trial is for women experiencing self-perceived thinning hair who wish to improve their hair growth. Participants will need to attend 5 to 6 visits over a period of 4 months and are comfortable with having their scalp numbed for the microneedling procedure that applies XVIE solution.

Inclusion Criteria

Ludwig Scale 1 to 2
Fitzpatrick skin types I to VI
Ability and willingness to comply with the study protocol
See 2 more

Exclusion Criteria

Change in other hair treatments within 3 months prior to the study
History of hair or scalp disorders that could interfere with study results
History of keloid formation or poor wound healing
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive the XVIE solution applied to the scalp by microneedling twice over a 4 month period

4 months
5 to 6 visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment, including photographic documentation and self-assessments

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • XVIE
Trial Overview The study tests the safety and effectiveness of XVIE solution when applied via microneedling on women's scalps. The treatment aims to enhance hair quality, volume, and thickness, assessed through photographic analysis across several visits.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: XVIE microneedling process applied to the scalp twice over a 4 month period.Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Restore Biologics Holdings, Inc. dba Xtressé

Lead Sponsor

Citations

Pilot Study to Evaluate the Efficacy and Safety of Xvie ...The goal of this study is to determine how safe and effective it is to improve hair growth using XVIE solution applied on the scalp of women ...
A Randomized Evaluator Blinded Study of Effect ...The results of this study show that Microneedling is a safe and a promising tool in hair stimulation both for male and female AGA and also is useful to treat ...
Pilot Study to Evaluate the Efficacy and Safety of XvieThe goal of this study is to determine how safe and effective it is to improve hair growth using XVIE solution applied on the scalp of women ...
Microneedling and Its Use in Hair Loss DisordersWhile evidence suggests that microneedling might improve hair loss, clinical data are of relatively low quality. With better study designs and ...
Microneedle-mediated therapies in hair lossMicroneedling offers several advantages in the treatment of hair loss. First, it significantly improves drug penetration by creating microscopic ...
Pilot Study to Evaluate the Efficacy and Safety of Xvie ...The goal of this study is to determine how safe and effective it is to improve hair growth using XVIE solution applied on the scalp of women ...
7.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/39483654/
Efficacy and safety of microneedling radiofrequency in ...Excellent improvement in hair growth was observed in 14 patients, fair improvement in seven patients, and no improvement in three patients without significant ...
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