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NCT06477172 · Acorn Biolabs Inc.

Autologous Hair Follicle Derived Secretome as Adjunct to Aesthetic Procedures

What this study is about

Non-interventional, multi-site, forward-looking, where both patients and doctors know the treatment given, observational, real-world study of autologous hair follicle secretome use.

View original scientific description

Non-interventional, multi-site, prospective, open-label, observational, real-world study of autologous hair follicle secretome use.

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

Inclusion criteria

  • Male and Female
  • Ages: 18-60
  • Any Fitzpatrick skin type
  • Planning a medical aesthetic procedure
  • For subjects receiving hair procedures (closed to enrollment):
  • Androgenic alopecia
  • Traction alopecia
  • Scarring alopecia
  • Stable use of any medication or supplement for hair loss, including finasteride, any other 5 α-reductase inhibitor, minoxidil, steroids, or hormonal products, during the 3 months prior to enrollment in the study is allowed.
  • No intention to start new hair growth medications or change dose of hair growth medications from the time of consent through the end of the study follow-up period.
  • Undergoing one of the following medical aesthetic procedures:
  • Laser resurfacing of the face (ablative or non-ablative) or Ellacor of the face (Ellacor closed to enrollment)
  • Tixel of the face
  • Keralase of the scalp (scalp treatment closed to enrollment)
  • Acne Scars and Surgery scars, either old or new as long as old scars are also being treated with ablative or non-ablative laser or microneedling (e.g. abdominoplasty, breast reduction/ reconstruction/enhancement, post-weight loss, etc.
  • Planning to use Acorn Autologous Hair Follicle Secretome cosmetic product

Exclusion criteria

  • Pregnant or Breastfeeding
  • Participation in an interventional clinical trial in the last 30 days
  • Use of other topical cosmetic products that may confound results
  • Use of retinoids within 7 days prior to facial procedure
  • For those receiving hair treatment, must not have had a hair transplant in the treatment area within the past 12 months
  • Any health condition that in the investigator's opinion should preclude participation in study

Where

  • Birmingham, Alabama
  • Scottsdale, Arizona
  • Beverly Hills, California
  • Fresno, California
  • Granite Bay, California
  • Los Angeles, California
  • Manhattan Beach, California
  • Marina del Rey, California
  • San Diego, California
  • Walnut Creek, California
  • West Hollywood, California
  • Lone Tree, Colorado

And 13 more locations — see the full list below.

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Mar 4, 2026 · Source of record for eligibility and locations

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1 of 500 participants interested
0% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

Preparing your pre-screening questions…

Study locations

Choose your preferred location, or select flexible during enrollment.

WITHDRAWN

Birmingham

Alabama

Location available
RECRUITING

Scottsdale

Arizona

Location available
WITHDRAWN

Beverly Hills

California

Location available
WITHDRAWN

Beverly Hills

California

Location available
RECRUITING

Fresno

California

Location available
RECRUITING

Granite Bay

California

Location available
RECRUITING

Los Angeles

California

Location available
WITHDRAWN

Manhattan Beach

California

Location available
RECRUITING

Manhattan Beach

California

Location available

And 22 more locations available.

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

Your information is protected and will only be shared with the research team.

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

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Looking for Post Procedural Erythema Treatment in Birmingham?

Join others in Alabama exploring innovative treatment options through clinical research

Post Procedural Erythema Treatment Options in Birmingham, Alabama

If you're searching for Post Procedural Erythema treatment in Birmingham, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Birmingham, Scottsdale, Beverly Hills and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Post Procedural Erythema. All study-related care is provided at no cost to participants.

Local Sites
3 locations in Alabama
Now Enrolling
Up to 500 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Post Procedural Erythema?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for Post Procedural Erythema

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This Post Procedural Erythema Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT06477172. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.