drugset / Trial / NCT03963102

Duration of Ameluz Application in Acral Actinic Keratoses Response

NCT03963102 ↗

Phase 4 Terminated 28 enrolled Royal Cornwall Hospitals Trust
RandomizedParallel-groupSingle-blindTreatment

Summary

A phase IV study of a single topical application of ALA for 3 hours or 4 hours to AK on acral sites (hands, feet, arms and legs), and subsequent measurement of clinical efficacy with corresponding PpIX fluorescence imaging.

Timeline

Start
2019-10-30
Primary completion
2024-03-31
Completion
2024-03-31

Outcome

Outcome not reported

Stopped: “Lack of appropriate personnel. Dr Xie abroad on other research, current PI Dr John Frewen not at main centre, no other available PI identified. Study suspended.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Aminolevulinic Acid Diagnostic / imaging agent — Topical

Indications