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临床试验/NCT04744103
NCT04744103撤回4 期

Trichloroacetic Acid as a Topical Treatment for Actinic Cheilitis

Nova Scotia Health Authority1 个研究点 分布在 1 个国家开始时间: 2023年9月15日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
撤回
试验地点
1
主要终点
Treatment Number

研究概览

简要总结

Actinic cheilitis is a condition of the lower lip characterized by grayish-white areas of discoloration and blunting of the demarcation between the cutaneous lip and the mucosa.

While many studies have compared treatment options for actinic cheilitis, there is still significant debate over how to best manage this condition. The chosen treatment regimen must result in complete remission while also preventing recurrence and malignant transformation. Current treatment options are vast, including both non-surgical and surgical options. Common topical therapies include 5-fluorouracil, imiquimod, ingenol mebutate and diclofenac. More recently, photodynamic therapy has been brought forward as a potential treatment modality. From a surgical perspective, a vermilionectomy is typically the procedure of choice.

TCA is a popular topical treatment for treat fine rhytides, hyperpigmentation, photodamage, and premalignant changes, such as actinic keratoses. Despite this, TCA is not commonly used for actinic changes on the lips. Here, the investigators propose an expansion of the application of TCA to be used in the treatment of actinic cheilitis.

详细描述

The proposed study will be a prospective cohort study of all patients with actinic cheilitis presenting to the study institution, the Queen Elizabeth II Health Science Center in Halifax, from March 1st 2021- March 1st 2023.

Patients will be consented to participate at the time of their initial consultation. They will fill out the demographics form, a preliminary survey and have the required photographs taken on that same day. A biopsy will be performed prior to treatment to establish the histological grade of their actinic cheilitis based on the degree of dysplasia. After the treatment is received, they will follow-up in 1 month for reassessment. At this point, a second treatment will be offered if clinical remission has not been achieved. Patients will continue TCA treatments at 1-month intervals until clinical remission is reached. Once remission is achieved, they will fill out the post-treatment questionnaire and have their second set of photos taken.

Final follow-up will occur 6 months post remission. At this point patients will be assessed for clinical recurrence. A third set of photos will be completed during this appointment.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Inclusion criteria will include all patients with actinic cheilitis that do not meet exclusion criteria.

排除标准

  • Exclusion criteria will include patients younger than 18 years of age and patients with a biopsy proven malignancy of the lip.

研究组 & 干预措施

TCA peal

Experimental

Patients will have their actinic cheilitis treated with a TCA peal.

干预措施: TCA (Drug)

结局指标

主要结局

Treatment Number

时间窗: 3 months

Establish the average number of treatments required to achieve remission.

Recurrence Rate

时间窗: 6 months

Determine the recurrence rate of actinic cheilitis following topical TCA treatment

Remission rate

时间窗: 3 months

Determine the remission rate of actinic cheilitis following topical TCA treatment.

Adverse Events

时间窗: 3 months

Identify the common adverse events, if any, associated with topical TCA lip peels and determine their incidence.

次要结局

  • patient satisfaction(6 months)
  • Healing Time(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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