A Randomized Controlled Trial of Topical 5% Niacinamide for Skin Cancer Prevention in Transplant Recipients

Trial statusRecruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorMarissa Lobl

About this trial

A Randomized Controlled Trial of Topical 5% Niacinamide for Skin Cancer Prevention in Organ Transplant Recipients

This study is designed to evaluate whether a topical 5% niacinamide cream can help prevent skin cancer in organ transplant recipients. Individuals who have received an organ transplant have a much higher risk of developing precancerous skin growths and skin cancers because of long-term immune-suppressing medications. Although sunscreen is an important part of sun protection, additional preventive approaches are needed. Early research suggests that niacinamide may help protect the skin, and this trial will examine whether a topical formulation provides benefit in this high-risk group.

The study will test whether daily use of topical 5% niacinamide reduces the number of actinic keratoses over 6 and 12 months and whether it decreases the development of new keratinocyte cancers when compared with sunscreen alone. The study will also evaluate how well the topical product is tolerated and whether it can be used consistently as part of a daily skin-care routine.

A total of 20 adult organ transplant recipients with a history of multiple actinic keratoses and at least one prior non-melanoma skin cancer will enroll in this 12-month, randomized, controlled trial. Participants will be assigned to receive either daily topical 5% niacinamide plus sunscreen or sunscreen alone. Skin examinations will be performed at 6 and 12 months using standardized mapping methods. Information on treatment tolerability, adherence, and any side effects will be collected through structured surveys, and any lesions suspicious for cancer will be evaluated by a board-certified pathologist.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Topical niacinamide 5% cream

    Drug

    Participants will be instructed to apply topical 5% niacinamide daily to any sun exposed areas.

  • Sunscreen

    Drug

    Sunscreen application daily, broad spectrum SPF 30, to any sun exposed areas

Treatment groups

20 Participants
are divided into 2 treatment groups
Group A: Sunscreen OnlyActive comparator 1 intervention
Group B: Sunscreen + NiacinamideExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Change in baseline AK count

Change in actinic keratosis count at 6 and 12 months from baseline, measured by standardized assessment and clinical quantification

Time frame
Baseline, 6 months and 12 months

Secondary outcomes

1

New NMSC

New nonmelanoma skin cancers (NMSC) at 6 months and 12 months

Time frame
6 months and 12 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Marissa Lobl

Lead sponsor

University of Pittsburgh

Sponsor institution