Rosemead, CANCT07155239Now EnrollingIRB Ready

Hidradenitis Suppurativa (HS) Clinical Trial in Rosemead, CA

Access cutting-edge hidradenitis suppurativa (hs) treatment through this clinical trial at a research site in Rosemead. Study-provided care at no cost to qualified participants.

Sponsored by Wynn Medical Center

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Expert Care in Rosemead

Access hidradenitis suppurativa (hs) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related hidradenitis suppurativa (hs) treatment provided free

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Check if you qualify for this hidradenitis suppurativa (hs) clinical trial in Rosemead, CA

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Why Participate?

  • No-Cost Study Care

  • Local to Rosemead

    Convenient for CA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Rosemead site if eligible
  4. 4Begin participation

About This Hidradenitis Suppurativa (HS) Study in Rosemead

Hidradenitis suppurativa (HS) is a long-lasting skin condition that causes painful lumps, abscesses, and tunnels in areas such as the armpits and groin. HS begins around the hair follicle; when the follicle becomes blocked and inflamed, new lesions form. Prior clinical studies of lasers that act on the hair follicle have shown improvement in HS symptoms, and a 1726-nm diode laser-designed to selectively heat oil glands within the follicle-has reduced inflammatory lesions in acne with good tolerability across many skin types. This study will test whether a 1726-nm diode laser can safely reduce inflammatory HS lesions in Hurley stage I-II disease. Adults with bilateral (right/left) affected areas will be randomized so that one side receives active laser treatment and the other side receives a sham procedure. Participants will have three treatment sessions over 8 weeks and follow-up through Week 24 while continuing their stable HS medications. The primary outcome is the percent change in abscess and inflammatory nodule counts on the treated side versus the sham side at Week 16. Secondary outcomes include validated HS responder scores, pain, quality of life, flare rate/antibiotic use, and safety. Results may support a non-ablative, follicle-directed option for early HS.

Sponsor: Wynn Medical Center

Who Can Participate

Inclusion Criteria

Adults 18-60 years; any sex; Fitzpatrick I-VI.
Clinical HS, Hurley I-II (Investigator confirmed).
At least one inflammatory nodule in a paired, bilateral region (axilla, groin/inguinal, inframammary, inner thigh, or buttock) within 4 weeks prior to baseline.
Able to read/speak English/Chinese/Spanish/Vietnamese and sign consent.
Willing/able to comply with visits, pre/post-care, standardized photography.
Agree to avoid new HS procedures/therapies in study areas through Week 24.
No laser contraindication; agrees to shave/clip hair before treatments.
Optional translational cohort: willing to undergo 4-mm punch biopsy at baseline and Week 16 from the randomized regions (separate consent).

Exclusion Criteria

Hurley III (extensive sinus tracts).
No qualifying nodule(s) in paired bilateral regions in past 4 weeks.
Prior device/procedure to target areas within 3 months (chemical peel, dermabrasion, microneedling/RF, other lasers/LBB, cryo/chemo-destruction)
Had Botulinum toxin in target areas within 3 months or planned during study.
Had systemic retinoid (e.g., isotretinoin) within 3 months.
Photosensitizing meds that, in PI's judgment, materially increase risk and cannot be held.
Pregnancy/breastfeeding/plans to conceive during study.
Active infection, still healing wounds (investigator judgment) in target areas.
History of keloids/hypertrophic scars, radiation to target areas, malignancy in target areas, diagnosed immunodeficiency, uncontrolled coagulation disorder or therapeutic anticoagulation that cannot be safely managed.
Excessive tanning or inability to avoid tanning.
Any condition (medical/mental) or prisoner status that in PI's opinion compromises safety or adherence.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Rosemead?

Yes, this clinical trial (NCT07155239) has an active research site in Rosemead, CA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Hidradenitis Suppurativa (HS) Treatment Options in Rosemead, CA

If you're searching for hidradenitis suppurativa (hs) treatment options in Rosemead, CA, this clinical trial (NCT07155239) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Rosemead research site is actively enrolling participants for this clinical trial. You'll receive care from experienced hidradenitis suppurativa (hs) specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all hidradenitis suppurativa (hs) clinical trials near you to find additional studies recruiting in your area.

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