Waltham, MANCT06868615Now EnrollingIRB Ready

Acne Clinical Trial in Waltham, MA

Access cutting-edge acne treatment through this clinical trial at a research site in Waltham. Study-provided care at no cost to qualified participants.

Sponsored by AVAVA, Inc.

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Expert Care in Waltham

Access acne specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related acne treatment provided free

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Check if you qualify for this acne clinical trial in Waltham, MA

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

Why Participate?

  • No-Cost Study Care

  • Local to Waltham

    Convenient for MA 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 Waltham site if eligible
  4. 4Begin participation

About This Acne Study in Waltham

A general protocol to treat a variety of dermatologic conditions and collect patient feedback. Primary outcome is the collection and analysis of patient questionnaires related to the overall experience of the device treatment. Secondary outcome measures include physician and subject evaluations in regards to improvement seen in the device as well as assessment of side effects.

Sponsor: AVAVA, Inc.

Who Can Participate

Inclusion Criteria

Male or female subjects between 18 to 70 years of age.
Dermatologic condition that can be addressed by the laser, including but not limited to:
Active Acne
Cutaneous Lesions such as Age or Sun Spots
Willingness to have digital photographs taken of treatment area(s) and agreement with use of photographs for presentation, educational, or marketing purposes.
Willingness to comply with the following during the study, including the follow-up period:
maintain consistent skin care regimen on treated areas.
cover treated areas or have very limited sun exposure and, if requested, use an approved sunscreen of SPF 50 or higher.
refrain from using systemic corticosteroids, according to Investigator discretion.
refrain from using topical corticosteroids, retinoids, or prescription skin-lightening medications on the treated areas, according to Investigator discretion.
refrain from any other procedures in the treatment areas.
Willingness and ability to comply with study instructions and return for required visits.
Subject has read and signed a written informed consent form.
Subject lives within 50 miles of study site.
Willingness to shave hair in intended treatment area

Exclusion Criteria

Skin pathology or condition that could interfere with evaluation of the study procedure, e.g.,
Systemic treatment prescribed within previous 6 months (e.g., oral medication such as isotretinoin)
Surgical treatment in the target areas within previous 6 months (e.g., laser surgery)
Active vitiligo, psoriasis, or eczema in the treatment area
Injection of dermal filler in the target areas within previous 1 month (e.g., collagen, hyaluronic acid filler)
Cosmetic procedures in the target areas within prior 3 months (e.g., laser, microdermabrasion, skin peel)
Topical treatment applied to target areas within the previous 1 month or according to Investigator discretion.
Active suntan and unable or unlikely to refrain from tanning within the follow-up period.
Artificial tanning in the target areas within the previous 1 month (e.g., spray, lotion, tanning bed) or intention to use artificial tanning within the follow-up period.
Active localized or systemic infection, or an open wound in area being treated.
Lesions in the treatment areas suspicious for malignancy (skin cancer, melanoma)
History of abnormal wound healing or abnormal scarring (e.g., hypertrophic or keloid)
History of connective tissue disease, such as lupus or scleroderma.
Any use of medication that is known to increase sensitivity to light according to Investigator's discretion (e.g., topicals that produce sensitivity to light may be used in areas other than the target area).
History of gold therapy.
History of disease stimulated by heat, such as recurrent herpes simplex or herpes zoster (shingles) in the treatment area, unless treatment is conducted following a prophylactic regimen.
History of radiation to the treatment area or currently undergoing systemic chemotherapy for the treatment of cancer.
For Female: Pregnancy or lactation, or intent to become pregnant within the study period.
Significant uncontrolled concurrent illness, such as diabetes mellitus or cardiovascular disease, e.g., uncontrolled hypertension.
History of immunosuppression/immune deficiency disorder or currently using immunosuppressive medications.
Current enrollment in a clinical study of any other unapproved investigational drug or device
Any other condition or laboratory value that would, in the professional opinion of the investigator, potentially affect response or participation in this clinical study, or would pose an unacceptable risk to the subject.

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 Waltham?

Yes, this clinical trial (NCT06868615) has an active research site in Waltham, MA 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.

Acne Treatment Options in Waltham, MA

If you're searching for acne treatment options in Waltham, MA, this clinical trial (NCT06868615) 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 Waltham research site is actively enrolling participants for this clinical trial. You'll receive care from experienced acne 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 acne clinical trials near you to find additional studies recruiting in your area.

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