The Effect of Topical Imipramine on Pain and Effectiveness of Topical Photodynamic Therapy

Last updated: April 23, 2024
Sponsor: Wright State University
Overall Status: Active - Recruiting

Phase

1

Condition

Squamous Cell Carcinoma

Sun Poisoning

Warts

Treatment

Vehicle

Imipramine

Clinical Study ID

NCT05688904
07286
  • Ages > 18
  • All Genders

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Male or female ages 18 and older
  • Skin type must be "Fair", Fitzpatrick type I to III, due to the presence of actinicdamage 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

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

Study Design

Total Participants: 24
Treatment Group(s): 2
Primary Treatment: Vehicle
Phase: 1
Study Start date:
January 19, 2023
Estimated Completion Date:
March 31, 2028

Connect with a study center

  • Wright State Physicians

    Fairborn, Ohio 45324
    United States

    Active - Recruiting

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