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NCT07401277 · ClinicalTrials.gov registry record · Phase 1

Actinic Keratoses Treated With 5-fluorouracil Plus Aluminum

A Phase 1 study, sponsored by West Virginia University.

Recruiting
Registry status
Phase 1
Development phase
32
Enrollment target

NCT07401277: Recruiting Phase 1 study, sponsored by West Virginia University.

NCT07401277 is a Phase 1 study that is actively recruiting participants, run by West Virginia University. The registered enrollment target is 32 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07401277, a Phase 1 study, is actively recruiting participants, sponsored by West Virginia University.

RECRUITING
Registry status
Phase 1
Development phase
32 participants
Enrollment target

Study Summary

This study is looking at a new way to treat actinic keratoses, which are rough, scaly spots on the skin caused by long-term sun exposure. These spots are common in older adults and, if not treated, can sometimes develop into a type of skin cancer. Doctors often treat areas with many of these spots by using a prescription cream called 5-fluorouracil (5-FU), which helps remove damaged skin cells. This study is testing whether adding aluminum chloride hexahydrate, a medication commonly used to stop bleeding during skin procedures, can improve how well the cream works. People who take part in this study will receive one of two treatments applied to their skin: Standard treatment with 5% 5-fluorouracil cream, or A combination of 5% 5-fluorouracil cream plus 15% aluminum chloride hexahydrate cream The treatment will be applied for one week. A dermatologist will examine the treated skin areas, count the number of actinic keratoses, and take photographs before treatment begins, shortly after treatment ends, and again about eight weeks later. These visits help researchers compare how well each treatment reduces the number of skin spots over time. The goal of this study is to learn whether adding aluminum chloride hexahydrate to standard treatment helps reduce actinic keratoses more effectively than standard treatment alone.

Primary Outcome

Total numerical counts of actinic keratoses (AKs) assessed and documented.

Interventions

  • DRUG 5% 5-fluorouracil (5-FU) powder
  • DRUG 5% 5-fluorouracil (5-FU) powder PLUS 15% Aluminum Chloride Hexahydrate (ACH)

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2026-02-06
Est. Completion 2027-08
Phase Phase 1
West Virginia University

122 total trials

What NCT07401277 shows while recruiting

NCT07401277 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower).

The record links to 0 conditions, and to 2 interventions - of which 5% 5-fluorouracil (5-FU) powder is the first listed.

NCT07401277 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07401277 about?

NCT07401277 is a clinical study titled "Actinic Keratoses Treated With 5-fluorouracil Plus Aluminum". This study is looking at a new way to treat actinic keratoses, which are rough, scaly spots on the skin caused by long-term sun exposure. These spots are common in older adults and, if not treated, can sometimes develop into a type of skin cancer. Doctors often treat areas with many of these spots ...

What is the current status of trial NCT07401277?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2026-02-06. Estimated completion is 2027-08.

What interventions are being tested in trial NCT07401277?

The interventions under investigation include: 5% 5-fluorouracil (5-FU) powder (DRUG), 5% 5-fluorouracil (5-FU) powder PLUS 15% Aluminum Chloride Hexahydrate (ACH) (DRUG).

Who is sponsoring clinical trial NCT07401277?

This trial is sponsored by West Virginia University, which has 122 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07401277's enrollment target sits among peer trials

32 1296th of 2000 higher than 679 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07401277, the US trial registry maintained by the National Library of Medicine. NCT07401277 (small enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.