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Lichen Planus clinical trials

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NCT ID: NCT04091698 Not yet recruiting - Oral Lichen Planus Clinical Trials

Clinical and Biochemical Assessment of the Effect of Topical Use of Coenzyme Q10 Versus Topical Corticosteroid in Management of Symptomatic Oral Lichen Planus: Randomized Controlled Clinical Trial

Start date: October 1, 2019
Phase: Phase 1
Study type: Interventional

The aim of the present investigation is to assess the clinical therapeutic effect of topical use of Coenzyme Q10 versus topical corticosteroid in management of symptomatic oral lichen planus and determine whether the effect, if any, was due to its antioxidant activity.

NCT ID: NCT03877679 Not yet recruiting - Oral Lichen Planus Clinical Trials

The Effect of Topical Curcumin Versus Topical Corticosteroid on Management of Oral Lichen Planus Patients

Start date: May 1, 2019
Phase: Phase 1
Study type: Interventional

Introduce a new anti-inflammatory and antioxidant paste preparation (curcumin paste) in the management of Oral lichen planus. - Assess the efficacy of this preparation on pain, clinical parameter and the level of IL-33 in saliva. - Compare the outcome of new preparation with the gold standard treatment (corticosteroids).

NCT ID: NCT03793634 Not yet recruiting - Oral Lichen Planus Clinical Trials

Evaluation of Topical Chamomile Versus Topical Triamcinolone Acetonide in Management of Oral Lichen Planus

Start date: January 15, 2019
Phase: Phase 1
Study type: Interventional

Using of herbal medications as topical chamomile which has antioxidant, anti-inflammatory and anticarcinogenesis effect with little side effects is the aim for the future treatment of OLP.

NCT ID: NCT03738176 Not yet recruiting - Oral Lichen Planus Clinical Trials

The Efficacy of Topical Sesame Oil Versus Topical Triamcinolone on Oral Lichen Planus and Salivary Level of Oxidative Stress Biomarker [MDA]

(MDA)
Start date: December 16, 2019
Phase: Early Phase 1
Study type: Interventional

use seseme oil and corticosteroid topically for two groups

NCT ID: NCT02332486 Not yet recruiting - Oral Lichen Planus Clinical Trials

Based on Metabonomics Dryness Pathogen Type of OLP: a Dynamic Study

OLP
Start date: January 2015
Phase: N/A
Study type: Interventional

Due to the change of life style, the incidence of oral cavity mucous membrane disease increased.In this study,been done a large number of pre-clinical practice and some experimental studies, based on the application of metabolomics technology to ultra-high liquid-mass spectrometry metabolomics analyzer as the core means, The metabolism of pattern recognition and combination of modern analytical techniques to measure blood and urine of patients with OLP-specific clearance of endogenous metabolites,and after the intervention of moss drink endogenous metabolites in the body as a whole group of. At the same time, the use of flow cytometry,,ELISA, immunohistochemistry and other modern technology, research OLP patients using clean moss drink before and after treatment of local lesions and peripheral blood CD4 +,CD8 + lymphocytes,Th1 cytokines (IFN-γ, TNF-α), Th2 cytokines (IL-4,10) the dynamic changes. From metabolomics, cellular immunology, inflammation mechanism perspective of local OLP lesions, peripheral blood and changes in endogenous metabolites in the process,,in-depth study of traditional Chinese medicine to drink clean moss multi-component multi-target treatment of this disease mechanism, is widely used in traditional Chinese medicine treatment of OLP provide a theoretical basis for the promotion of Chinese medicine Qingxian Yin in the oral mucosal disease in the application, effectively solve clinical practice problems.

NCT ID: NCT01083420 Not yet recruiting - Oral Lichen Planus Clinical Trials

The Efficacy of Topical Minocycline in Managing Symptomatic Oral Lichen Planus

Start date: March 2010
Phase: Phase 3
Study type: Interventional

The aim of the present study is to assess the clinical efficacy of topical minocyclin in managing of symptoms associated with oral lichen planus (OLP). The rationale of the study is based on our previous studies demonstrating the beneficial effect of minocyclin mouthwash on recurrent aphthous stomatitis. The planned study will be a randomized controlled, cross-over trail. Patients with symptomatic OLP will randomly receive minocycline or dexamethasone rinses. The patients will rinse and expectorate 5 ml of the 1st mouthwash 4 times daily for 14 days. Subjects will complete a daily follow-up form that includes data regarding the daily intensity of pain (using VAS) caused by OLP and regarding possible side effects. After a washout period (at least 14 days) the patients will repeat the protocol with the second mouthwash.

NCT ID: NCT01041625 Not yet recruiting - Lichen Planus Clinical Trials

Pilot Study of Apremilast (CC-10004) in the Treatment of Moderate to Severe Lichen Planus

Start date: February 2010
Phase: Phase 2
Study type: Interventional

This study is designed to demonstrate to efficacy and safety of Apremilast 20mg oral administration twice daily over 12 weeks in subjects with moderate to severe lichen planus. The hypothesis is that the subjects will achieve a significant clinical improvement in their skin disease according to a specialized physician grading scale.