Patient Guide: Autologous Hair Follicle Derived Secretome as Adjunct to Aesthetic Procedures

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 34 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06477172
Status: 🟢 Enrolling Now
Condition: Post Procedural Erythema
Phase: Not Specified

Where You Can Participate

This study is available at 34 locations across the country.

Top locations include:
  • • Scottsdale, Arizona
  • • Beverly Hills, California
  • • Fresno, California
  • • And 31 more locations

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Autologous Hair Follicle Derived Secretome as Adjunct to Aesthetic Procedures - Join Clinical Trial NCTNCT06477172

How to Join This Clinical Trial - NCTNCT06477172

Learn how to participate in this Not Specified trial studying an investigational therapy for Post Procedural Erythema. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Post Procedural Erythema. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Post Procedural Erythema
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06477172 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 34 locations. Find a study site near you:

Clinical Research Site

Scottsdale, Arizona 85260 - United States

Status: RECRUITING

Clinical Research Site

Beverly Hills, California 90211 - United States

Status: RECRUITING

Clinical Research Site

Fresno, California 93720 - United States

Status: RECRUITING

Clinical Research Site

Granite Bay, California 95746 - United States

Status: RECRUITING

Clinical Research Site

Manhattan Beach, California 90266 - United States

Status: RECRUITING

Clinical Research Site

Manhattan Beach, California 90266 - United States

Status: RECRUITING

Clinical Research Site

Marina del Rey, California 90292 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Redondo Beach, California 90277 - United States

Status: RECRUITING

Clinical Research Site

West Hollywood, California 90069 - United States

Status: RECRUITING

Clinical Research Site

West Hollywood, California 90069 - United States

Status: RECRUITING

And 24 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Post Procedural Erythema:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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