New York, NYNCT07187297Now EnrollingIRB Ready

Wrinkle Clinical Trial in New York, NY

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

Sponsored by Bausch Health Americas, Inc.

Quick Self-Assessment

See if you qualify for this New York location

Preparing your pre-screening questions…

Expert Care in New York

Access wrinkle specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related wrinkle treatment provided free

Apply for This New York Location

Check if you qualify for this wrinkle clinical trial in New York, NY

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to New York

    Convenient for NY 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 New York site if eligible
  4. 4Begin participation

About This Wrinkle Study in New York

A prospective, 180-day, randomized, multicenter, independent blinded evaluators, controlled study of treatment with the Thermage FLX System

Sponsor: Bausch Health Americas, Inc.

Who Can Participate

Inclusion Criteria

Be an adult female or male, ≥30 - ≤60 years of age. Have mild-to-moderate skin laxity of the neck, abdomen, upper arms, and/or face, and/or mild-to-moderate lines and/or wrinkles of the neck and/or face assessed as follows: Neck: Mild-to-moderate neck skin laxity as defined by a score of 1 to 6 on the 10-point Facial Laxity Rating Scale (scored 0-9) Mild-to-moderate neck wrinkles as defined by a score of 1 to 6 on the 10-point Fitzpatrick Wrinkle Scale (scored 0-9) Abdomen: Mild-to-moderate abdomen skin laxity as defined by a score of 1 or 2 on a 4-point Abdominal Laxity Scale (scored 0-3) Upper arms: Mild to moderate upper arms skin laxity as defined by grade 2 or 3 on the 5-grade IBSA Inner Upper Arm Laxity Scale Face: Mild-to-moderate facial skin laxity as defined by a score of 1 to 6 on the 10-point Facial Laxity Rating Scale (scored 0-9) Mild-to-moderate facial wrinkles as defined by a score of 1 to 6 on the 10-point Fitzpatrick Wrinkle Scale (scored 0-9) Females of childbearing potential must have a negative urine pregnancy test. Females who have experienced menarche and who are not postmenopausal (either confirmed via FSH testing or who have not menstruated for 2 years or more without an alternative medical cause) or surgically sterile will be considered of childbearing potential. Females of childbearing potential must agree to use an acceptable method of birth control for the duration of the study. Acceptable methods of birth control are oral and other systemic contraceptives, condoms only, intrauterine device, double-barrier methods, bilateral tubal ligation, partner vasectomy, and abstinence. Have no clinically abnormal findings based on the medical history as determined by the study investigator. Be able to follow the study instructions, be available on the specific required study visit days, and be willing to complete all study visit procedures and assessments. Understand the research nature of this study and sign an informed consent document prior to the performance of any study-specific procedure or assessment. Agree to not undergo excluded procedures (i.e., energy-based device treatments, injectables, or plastic surgery) on the study treatment areas for the duration of study. Participant has a body mass index (BMI) ≤30.

Exclusion Criteria

Participant is pregnant or breast feeding or trying to become pregnant for 3 months prior to the screening visit or during the study. Participant has given birth within 3 months prior to the screening visit. Participant has an anticipated need for procedures, surgery, overnight hospitalization, or other events that would prevent the participant from making the required visits during the study. Participant has a pacemaker, internal defibrillator, or other implanted electronic device. Participant has an implant in the target treatment zone(s). Participant has had radiation therapy in the target treatment zone(s). Participant has had 1 or more prior cosmetic procedures in the target treatment zone(s) including: Thermage or any energy-based device procedure, derm abrasion, or chemical peel on any treatment area within 6 months prior to the screening visit. Short-acting neurotoxins within 6 months prior to the screening visit. Long-acting neurotoxins within 9 months prior to the screening visit. Hyaluronic acid filler ≤1 year prior to the screening visit. Semi-permanent or permanent fillers at any time prior to the screening visit. Plastic surgery within 1 year prior to the screening visit.

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 New York?

Yes, this clinical trial (NCT07187297) has an active research site in New York, NY 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.

Wrinkle Treatment Options in New York, NY

If you're searching for wrinkle treatment options in New York, NY, this clinical trial (NCT07187297) 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 New York research site is actively enrolling participants for this clinical trial. You'll receive care from experienced wrinkle 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.

Ready to Join in New York?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · New York, NY