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Active clinical trials for "Acne Vulgaris"

Results 541-550 of 597

Pharmacokinetics Study of Dapsone-Adapalene Fixed Combination Gel in Acne

Acne Vulgaris

This study will investigate the pharmacokinetics, safety and tolerability of dapsone and adapalene following topical administration of 2 formulations of dapsone/adapalene fixed combination gel, dapsone 5% gel (ACZONE®), and adapalene 0.3% gel (Differin®) in subjects with acne vulgaris.

Withdrawn10 enrollment criteria

Relationship of Whole Blood Zinc Levels to Acne Severity

Acne Vulgaris

Acne Vulgaris is one of the most common dermatologic diagnoses in the world. A number of studies have been conducted comparing serum zinc levels with acne vulgaris; however, no studies have yet been done in the Philippine setting. The objective of this study is to determine the relationship between whole blood zinc levels and the severity of acne vulgaris in Filipino patients and normal controls who are 18-25 years old.

Completed13 enrollment criteria

Profiling the Skin Microbiome in Response to Altreno in Acne Patients

AcneHealthy

The study objective is to characterize the shift in the diversity and abundance of the skin microbial community at baseline and in response to Altreno monotherapy as compared to benzoyl peroxide (BPO) 2.5% leave-on gel monotherapy in acne patients.

Completed9 enrollment criteria

Efficacy of Epiduo and Treatment Adherence of Adolescent Patients With Inflammatory Acne

Acne

The purpose of this observational study is to assess the efficacy of Epiduo and patient adherence under daily clinical practice conditions in adults and adolescents (12 to 20 years) with moderate inflammatory acne using this drug first time in topical monotherapy.

Completed6 enrollment criteria

A Study to Evaluate the Potential of Tazarotene Foam to Cause a Reaction When Applied to the Skin...

Acne Vulgaris

The purpose of this study is to evaluate the potential of Tazarotene Foam to induce a phototoxic reaction when exposed to UV and VIS light on skin of healthy volunteers.

Completed34 enrollment criteria

Risk Minimisation Study for Diane-35 and Its Generics

Acne Vulgaris

The study will be an observational, cross-sectional study of knowledge, understanding, and self-reported behavior among a sample of physicians with recent experience in prescribing Diane-35 or its generics in a total of five European countries. The primary objective of this study is to measure physician knowledge and understanding of the key information contained in the Diane-35 educational material: Patient information card, and Prescribers' Checklist. Specifically, the following objectives will be addressed: Investigate whether physicians have received any educational material related to Diane-35 or its generics Assess physicians' knowledge and understanding of key safety information pertaining to the patient information card Assess physicians' knowledge and understanding of key safety information pertaining to the following areas: Contraindications relevant to thromboembolism Risk factors for thromboembolism Signs and symptoms of thromboembolism

Completed1 enrollment criteria

Clinical Study for the Evaluation of P-3075 Cream on Acne Treatment

Acne

Primary end point of the study is the clinical and non-invasive instrumental evaluation of the activity of P-3075 cream on subjects with acne: 20 subjects with a mild/moderate grade and 20 subjects with a moderately severe/severe grade, according to Cunliffe' classification. Secondary end-points are the cosmetic acceptability and efficacy evaluation by the volunteers and the local tolerability assessed by the investigator and the subjects.

Completed14 enrollment criteria

Long-term Study of Epiduo in Patients With Moderate to Severe Acne

Acne Vulgaris

This observational study is designed to assess the long-term efficacy and safety of Epiduo (alone or in combination with other drugs) under daily clinical practice conditions in patients with moderate to severe inflammatory acne. In addition, the effect of Epiduo on quality of life and patient adherence will be assessed under marketed conditions.

Completed8 enrollment criteria

A Study to Evaluate the Bioavailability of Tazarotene Foam, 0.1%, and Tazorac Gel, 0.1%, in Subjects...

Acne Vulgaris

The purpose of this study is to assess systemic exposure of a new foam formulation of tazarotene, 0.1% compared with Tazorac Gel, 0.1%. The study design and dosing regimen are based on previous clinical studies with Tazorac Gel and Tazorac Cream.

Completed26 enrollment criteria

Management of Side-Effects of Anti-Acne Treatment by a Cosmetic Routine

Acne

Retinoid-based topical acne treatment may induce local tolerance issues such as erythema, dryness, stinging and burning sensations that may reduce adherence and efficacy. The tested regimen (cream and cleanser) has been specifically developed to rebalance the skin microbiome and compensate side-effects of topical treatments (hydration, skin barrier repair) together with an action on skin imperfections and marks. This open-label study was conducted in subjects aged 12 years and over with sensitive skin (>2 on a sensitivity composite score from 0-3) treated for at least one month with the fixed-dose gel combination and presenting with treatment-related skin intolerance.

Completed15 enrollment criteria
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