Fairborn, OHNCT05688904Now EnrollingIRB Ready

Imipramine Clinical Trial in Fairborn, OH

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

Sponsored by Wright State University

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Expert Care in Fairborn

Access imipramine specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related imipramine treatment provided free

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Check if you qualify for this imipramine clinical trial in Fairborn, OH

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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 Fairborn

    Convenient for OH 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 Fairborn site if eligible
  4. 4Begin participation

About This Imipramine Study in Fairborn

The purpose of this study is testing the use of topical Imipramine in combination with topical photodynamic therapy's (PDT) effect on pain following treatment. PDT is a commonly used treatment in dermatology for patients who have many pre-cancers (actinic keratosis-AKs) on their skin. These are both FDA-approved treatments, but this study is evaluating their use in combination, which has not been evaluated in the past. The investigators have been doing studies using animals that suggest that imipramine might make the PDT less painful and might help it work better. In order to participate, the subject and their dermatologist have decided that they would benefit from PDT to treat their skin due to many AK precancerous lesions. Please note that neither PDT nor imipramine are experimental treatments, but treating their skin with imipramine before PDT is a new approach.

Sponsor: Wright State University

Who Can Participate

Inclusion Criteria

Male or female ages 18 and older
Skin type must be "Fair", Fitzpatrick type I to III, due to the presence of actinic damage in this population.
Subjects need to have a physician's order to receive PDT treatment on their face, scalp or forearms.
Willing to participate and understand the informed consent document.
Willing to avoid excess sun exposure/tanning beds to the area to be treated with PDT.

Exclusion Criteria

Those currently taking any tricyclic antidepressants (TCAs)
Those currently taking any selective serotonin reuptake inhibitor (SSRI)
Those with porphyria
Large tattoos in the treated areas
Pregnancy or nursing
Taking any oral or topical medications that could interfere with the PDT (Appendix A)
Active rashes in the area

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 Fairborn?

Yes, this clinical trial (NCT05688904) has an active research site in Fairborn, OH 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.

Imipramine Treatment Options in Fairborn, OH

If you're searching for imipramine treatment options in Fairborn, OH, this clinical trial (NCT05688904) 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 Fairborn research site is actively enrolling participants for this clinical trial. You'll receive care from experienced imipramine 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 imipramine clinical trials near you to find additional studies recruiting in your area.

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