Actively Recruiting
Clinical and Molecular Correlates of Response to First Line Treatment in Lichen Planus
Led by University of Aberdeen · Updated on 2024-04-10
110
Participants Needed
2
Research Sites
242 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Lichen planus is a common inflammatory (swelling and pain of tissue) disease in the general population that affects mostly the mouth although skin and genital areas can also be affected. It can cause considerable discomfort during activities such as eating, talking and tooth brushing and may impair sexual function with an overall deleterious impact on quality of life. There is also increased evidence of cancer in a subtype of lichen planus. Therefore, treatment is essential in these patients to control the symptoms and improve the quality of life. Locally applied steroids are the first line medicines used in the treatment of patients with lichen planus. This medicine can only control the symptoms, but cannot cure the disease. In addition, this treatment cannot be effective in all patients with lichen planus. This may be attributed to differences in host factors, mouth bacteria and individual host responses to bacteria. The exact cause of this disease is also unknown. New studies have shown changes in the balance of mouth bacteria and host responses to bacteria in patients with lichen planus. So the main purpose of our study is to identify clinical(age, gender, related medical conditions, oral health and the presence of deleterious habits like smoking and alcohol consumption), molecular(analysis of oral microbes and immune markers) and histological factors (change within tissue) associated with poor response in lichen planus patients undergoing treatment with locally applied steroid medicines. Overall, knowledge of these factors associated with disease progression is sparse, which limits progress in the realm of development of novel and personalised treatment strategies. In this study, we explore the individual and combined role of different markers in lichen planus for improving diagnosis, predicting disease progression and treatment effectiveness.
CONDITIONS
Official Title
Clinical and Molecular Correlates of Response to First Line Treatment in Lichen Planus
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged more than 18 years, with confirmed histopathological diagnosis of lichen planus and undergoing topical steroid therapy.
- Participants who have the capacity to consent.
- Participants who show a willingness to attend an initial appointment and a follow-up post-treatment appointment.
You will not qualify if you...
- Patients on systemic steroids and other immunosuppressive agents for the treatment of lichen planus.
- Cases of graft versus host disease or those suffering from other systemic inflammatory conditions mimicking lichen planus (e.g. connective tissue disease).
- Pregnant and lactating participants.
- Inability to consent.
AI-Screening
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Trial Site Locations
Total: 2 locations
1
University of Aberdeen
Aberdeen, Aberdeen, Scotland, United Kingdom, AB24 3FX
Enrolling by Invitation
2
Aberdeen Dental School
Aberdeen, United Kingdom, AB25 2ZR
Actively Recruiting
Research Team
D
Dr Karolin Hijazi
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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