Clinical trial · Interventional
Menthol for PDT Pain Relief
A Randomised Double Blind, Placebo Controlled Study of the Efficacy of Topical Menthol for Pain Relief During Topical Photodynamic Therapy
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Topical photodynamic therapy (PDT) is widely used to treat superficial non-melanoma skin cancer (NMSC) and dysplasia, notably actinic keratosis and may also be effective in a range of other dermatological conditions. A major limitation of PDT is pain during irradiation. A lack of knowledge of the mechanism of PDT-induced pain has limited the development of effective approaches for prevention or relief of this adverse effect. The investigators have investigated the possible efficacy of menthol for PDT pain ex vivo and will now study this in a clinical trial. This proposal describes the prospective randomised double blind, placebo controlled clinical trial that will be undertaken to investigate the use of topical menthol for PDT-induced pain relief in patients with actinic keratosis of the face and scalp who will be attending general dermatology and PDT outpatient clinics at Ninewells Hospital, Dundee.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Actinic Keratosis | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Aqueous Cream | Drug | — | UNRESOLVED |
| Menthol | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Menthol
- description
- 5% menthol in aqueous cream (Dermacool Forte)
- interventionNames
- Drug: Menthol
- type
- PLACEBO_COMPARATOR
- label
- Placebo
- description
- Aqueous cream
- interventionNames
- Drug: Aqueous Cream
Primary outcomes (1)
- measure
- Pain immediately after PDT assessed by VAS score
- timeFrame
- 24h
- description
- pain immediately after and at 3, 6 and 24 h after PDT assessed by VAS score
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 100 Years
Show eligibility criteria text
Inclusion Criteria: A subject will be eligible for inclusion in this study only if all of the following criteria apply: 1. Adults \>18 years. Target population is men or women ≥50 years (only post-menopausal women) 2. Presence of actinic keratoses (AK) on the face and scalp involving both right and left comparable sites. 3. Free of significant physical abnormalities (e.g. tattoos, dermatoses) in the potential treatment area that may cause difficulty with examination or final evaluation. 4. Able to understand and adhere to protocol requirements. Exclusion Criteria: 1. Unable to give written informed consent. 2. Allergy to menthol, aqueous cream or excipients 3. Participation in a drug trial or other interventional study within 30 days of recruitment to this study 4. Pre-menopausal women, pregnancy, breast feeding, planning to conceive 5. Chronic pain
References
Publications (0)
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