85 Participants Needed

Angiogenesis Study for Skin Conditions

Recruiting at 3 trial locations
HK
Overseen ByHanna Kim
Age: Any Age
Sex: Any
Trial Phase: Academic
Sponsor: University of California, Irvine
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 explore how abnormal blood vessel growth (angiogenesis) affects skin conditions such as port wine stains, hemangiomas, rosacea, and psoriasis. Researchers will analyze skin samples to identify patterns and potential treatment targets for these diseases. Participants must be at least 16 years old and willing to undergo a skin biopsy, which involves removing a small skin sample for testing. Individuals with a clinically diagnosed skin condition may find this study suitable. As a Phase 2 trial, the research measures the treatment's effectiveness in an initial, smaller group, offering participants a chance to contribute to important advancements in skin condition treatments.

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

The trial information does not specify whether you need to stop taking your current medications. It's best to ask the trial coordinators for more details.

Why are researchers excited about this trial?

Researchers are excited about this trial because it explores the role of angiogenesis—a process where new blood vessels form—in dermatologic diseases. Unlike standard treatments that primarily address symptoms or inflammation, this approach could uncover new therapeutic targets by examining how blood vessel growth affects skin conditions. By analyzing skin biopsy samples, scientists aim to understand the underlying mechanisms, potentially leading to innovative treatments that address the root cause of these diseases rather than just managing their symptoms.

Who Is on the Research Team?

KK

Kristen Kelly, MD

Principal Investigator

University of California, Irvine

Are You a Good Fit for This Trial?

Inclusion Criteria

willing to have a skin biopsy

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Sample Collection and Analysis

Biospecimens from dermatologic diseases are collected and analyzed for angiogenic markers. Genetic analysis may be performed on select specimens.

4 weeks

Follow-up

Participants are monitored for safety and effectiveness after sample collection and analysis

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Skin Biopsy

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: dermatologic diseasesExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of California, Irvine

Lead Sponsor

Trials
580
Recruited
4,943,000+

Beckman Laser Institute University of California Irvine

Collaborator

Trials
78
Recruited
5,000+