Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Rosacea from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 12
- Active, not recruiting: 3
- Completed: 23
- Other: 12
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT05928169 — Determinants of Chronic Inflammatory Skin Disease Trajectories
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospital Schleswig-Holstein |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Atopic Dermatitis; Psoriasis; Lichen Planus; Alopecia Areata; Hidradenitis Suppurativa |
| Interventions |
Although it is well known that the clinical expression and course of chronic inflammatory skin diseases are highly variable, there are insufficient epidemiological data on this, and the factors that determine the manifestation, clinical features and course are also largely unknown. There are currently no reliable markers that could predict or delineate patient subgroups to support patient manag…
NCT05942248 — The Use of Image-Based Computer Gradings in the Analysis of Acne, Rosacea, Melasma, and Seborrheic Dermatitis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Integrative Skin Science and Research |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Acne; Melasma; Rosacea; Seborrheic Dermatitis |
| Interventions |
The study is conducted to determine if image-based computer grading can of acne, melasma, rosacea and seborrheic dermatitis correlate well to expert based clinical severity grading.
NCT06072066 — Effects of Oral Supplement Containing L-Histidine and Antioxidants on the Skin Barrier Function and Systemic Inflammation in Rosacea
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Integrative Skin Science and Research |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea; Systemic Inflammation |
| Interventions |
The purpose of this study is to evaluate how supplementation will alter the skin and the gut barrier and inflammation in those with rosacea.
NCT06312813 — Evaluating Use of Topical Imipramine and Amitriptyline in Reducing Ultraviolet B Light-Induced Redness in Patients With Rosacea
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Wright State University |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea |
| Interventions | ; ; |
Rosacea is a common skin condition associated with easy blushing and red face; many patients with rosacea react to sunlight with increased redness. The purpose of this study is to determine if the use of a topical medication will help reduce sunlight induced redness and irritation in patients with rosacea.
NCT06466018 — Research Into Diagnostic and Prognostic Molecular and Imaging Biomarkers of Ocular Disorders Associated With Neurovascular Deregulation: Biocor Cohort
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Clinact |
| Enrollment | 400 |
| Study Type | INTERVENTIONAL |
| Conditions | Ocular Rosacea; Pachychoroid Disease |
| Interventions |
BIOCOR is an interventional clinical trial whose main objectives are Objectif are identify molecular biomarker(s) of ocular rosacea and pachychoroid. Endpoints are : Correlation between pachychoroidosis (defined by choroidal phenotype parameters in OCT and autofluorescence) or the stage of ocular rosacea (ROSCO(29) definition) and biological markers selected on the basis of preclinical work (an…
NCT06801717 — Rosacea Radiofrequency Microneedling
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Miami |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea, Papulopustular; Rosacea, Erythematotelangiectatic |
| Interventions | ; |
There are 3 main objectives of this proposal as follows: (1) to assess the efficacy of radiofrequency microneedling in the treatment of erythematotelangiectatic and or papulopustular rosacea, (2) to determine the potential for combination treatment of radiofrequency microneedling with the 532 nm KTP laser, and (3) identify potential novel therapeutic strategies for the treatment of rosacea.
NCT06952517 — Efficacy and Safety of Topical Clascoterone (WINLEVI) Cream 1% in Patients With Facial Acneiform Rosacea
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Narrows Institute for Biomedical Research |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Papular-pustular Rosacea; Papulopustular Rosacea (PPR); Papulopustular Rosacea |
| Interventions |
To demonstrate the efficacy of Clascoterone cream 1% in reducing the size of sebaceous glands in study participants with acneiform rosacea.
NCT07106957 — Efficacy and Safety Evaluation of CICAPLAST BAUME B5+ on Rosacea Accompanied by Sensitive Skin
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Beijing Sino-German Union Cosmetic Institute Co., Ltd. |
| Enrollment | 72 |
| Study Type | INTERVENTIONAL |
| Conditions | Erythematous Telangiectatic Rosacea |
| Interventions | ; |
In total, 72 eligible research participants were recruited in this 56-day study. The participants were divided into two groups-namely the Experimental Group and the Control Group-according to stratified randomization, with 36 participants in each group. Finally, 30 participants in each group were expected to complete the study.
In this study, for patients with rosacea accompanied by sensitive …
NCT07296497 — Acupuncture for Refractory Rosacea: A Study on Its Effectiveness and Safety
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Xiangya Hospital of Central South University |
| Enrollment | 104 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea |
| Interventions | ; |
This study is a randomized, multicenter, sham-controlled clinical trial designed to evaluate the efficacy and safety of acupuncture for patients with refractory rosacea. A total of 104 participants will be enrolled and randomly assigned in a 1:1 ratio to the acupuncture group or the sham acupuncture group (52 participants in each group, regardless of sex). The primary aim is to determine whethe…
NCT07343635 — The Efficacy and Safety of Anti-inflammation Treatment (Hirudoid Introduction Followed by Yellow Light Therapy) Combined With Tofacitinib and Doxycycline in Chinese Adult Patients With Mild to Moderate Erythematous Telangiectatic Rosacea
| Status | Recruiting |
| Phase | N/A |
| Sponsor | The Fourth Affiliated Hospital of Zhejiang University School of Medicine |
| Enrollment | 186 |
| Study Type | INTERVENTIONAL |
| Conditions | Erythematotelangiectatic Rosacea |
| Interventions | ; ; |
The efficacy and safety of anti-inflammation treatment (Hirudoid introduction followed by yellow light therapy) combined with tofacitinib and doxycycline in Chinese adult patients with mild to moderate erythematous telangiectatic rosacea: A prospective parallel controlled single-blind cohort study
NCT07637032 — Clinical Study of a Facial Cream for Rosacea
| Status | Recruiting |
| Phase | N/A |
| Sponsor | ChinaNorm |
| Enrollment | 76 |
| Study Type | INTERVENTIONAL |
| Conditions | Facial Rosacea |
| Interventions | ; |
This study aimed to evaluate the efficacy, tolerability, and safety of Eucerin Skin Relief Multi-Repair Cream containing the active ingredient SenSiCel™ in improving facial rosacea. A single-center, randomized, negative-controlled clinical intervention design was adopted. A total of 76 Chinese women aged 20-50 years with Fitzpatrick skin types III-IV and mild-to-moderate rosacea (IGA score 2-3,…
NCT07341087 — Skin Inflammation in (Peri)Menopause: A Probiotic Intervention Proof of Concept Trial
| Status | Recruiting |
| Phase | N/A |
| Sponsor | King’s College London |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Skin Inflammation; Immunosenescence; Inflammation; Skin Health; Eczema |
| Interventions | ; |
This study will explore whether a daily probiotic drink containing Lactobacillus casei Shirota (LcS) can help improve immune function and reduce inflammation in women going through the menopausal transition. Hormonal changes during this stage of life can affect the immune system, gut health, and skin, sometimes leading to increased inflammation or conditions such as eczema, acne or rosacea.
Pa…
Active, Not Recruiting
NCT04108897 — Analysis of the Microbiome in Rosacea
| Status | Active, not recruiting |
| Phase | Early Phase 1 |
| Sponsor | Johns Hopkins University |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea |
| Interventions | ; |
The skin and gut microbiome of rosacea patients differs from individuals without rosacea and that the microbiome suffers from unique derangements in rosacea patients following antibiotic therapy.
This study was proposed to examine microbial signatures of the skin and gut microbiome in patients with moderate to severe rosacea and to identify differences between microbe communities in patients w…
NCT05296837 — Ocular Rosacea Biome Study
| Status | Active, not recruiting |
| Phase | Phase 4 |
| Sponsor | University of California, San Francisco |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Ocular Rosacea; Antimicrobial Resistance |
| Interventions | ; ; |
Ocular rosacea is an inflammatory disease of the eyelids and ocular surface. Like the facial disease, the ocular condition is chronic and recurrent. Sequelae of ocular rosacea vary from mild to severe. Ocular rosacea may cause chronic eye redness, blepharitis, recurrent chalazia, dry eye, corneal erosion, corneal vascularization, and corneal ulceration. Rosacea affecting the cornea can result i…
NCT07667972 — Microfocused Ultrasound for Facial Pigmentary Diseases and Rosacea
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Xiangya Hospital of Central South University |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Melasma; Rosacea; Periorbital Hyperpigmentation; Melanosis; Lichen Planus Pigmentosus |
| Interventions | ; |
This clinical study will evaluate the efficacy and safety of microfocused ultrasound treatment in patients with facial pigmentary diseases and rosacea.
The study includes two independent disease cohorts: a facial pigmentary disease cohort and a rosacea cohort. Participants in each cohort will be randomly assigned to receive either active microfocused ultrasound treatment or sham stimulation. S…
Not Yet Recruiting
NCT06763367 — Clinical Evaluation and Study of the Efficacy of a Centella Asiatica-Infused Facial Mask on Discosmetic Dermatosis
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Nanjing First Hospital, Nanjing Medical University |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea; Acne; Centella; Melasma |
| Interventions |
The purpose of this study was to investigate the efficacy and safety of repairing facial mask containing Asiaticum asiatica in treating disjunctive skin diseases. A multi-center randomized double-blind self-half face control method was used. A computer-generated randomization method was used. Each cheek was randomly assigned to receive the snow glycoside mask and the control group.
NCT07290426 — Vbeam Pro Pulse Dye Laser for the Treatment of Vascular Conditions
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Candela Corporation |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea; Vascular Diseases; Port-Wine Stain |
| Interventions |
This is a clinical study to evaluate the safety and performance of the Vbeam Pro Laser System for the treatment of vascular indications, including rosacea and port wine stain birthmarks.
NCT07600424 — Transcutaneous Auricular Vagus Nerve Stimulation Treatment for Rosacea
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Brigham and Women’s Hospital |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea; Rosacea, Erythematotelangiectatic; Flushing |
| Interventions |
A single arm, pilot study among individuals with rosacea and at least moderate flushing or rednesss will be enrolled in a 4-week trial of taVNS. The particicpants will be followed for an additional 4-weeks following the intervention period to evaluate the durability of the results
NCT07681271 — A Phase 2 Study to Investigate the Efficacy, Safety and Tolerability of Remibrutinib (LOU064) in Adult Patients With Papulopustular Rosacea (PPR)
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Papulopustular Rosacea |
| Interventions | ; |
This Phase 2 study aims to evaluate whether Bruton’s tyrosine kinase (BTK) inhibition with remibrutinib can produce a clinically meaningful reduction in inflammatory lesions in adults with moderate-to-severe papulopustular rosacea, while also assessing safety and tolerability of remibrutinib in this indication.
NCT07521462 — Dermocosmetic Treatment for Facial Redness in Rosacea With or Without Laser Therapy
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | ISISPHARMA |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea, Erythematotelangiectatic; Rosacea Subtype 1 (Erythematotelangiectatic) |
| Interventions | ; ; |
The aim of this clinical study is to evaluate the effectiveness and safety of a dermocosmetic product in reducing facial redness and visible blood vessels associated with erythematotelangiectatic rosacea.
Investigators will compare the dermocosmetic product to a placebo applied to opposite sides of the face, when used alone and in combination with laser treatment.
Participants will apply the …
Enrolling by Invitation
NCT07443202 — Study of Lotilaner Ophthalmic Gel in Patients With Ocular Rosacea (KORE)
| Status | Enrolling by invitation |
| Phase | Phase 2 |
| Sponsor | Tarsus Pharmaceuticals, Inc. |
| Enrollment | 155 |
| Study Type | INTERVENTIONAL |
| Conditions | Ocular Rosacea |
| Interventions | ; |
To evaluate lotilaner treatment in patients with ocular rosacea.
NCT07606820 — Real-World Study of Cligabalin(HSK16149) for the Treatment of Neurogenic Rosacea
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | The First Affiliated Hospital with Nanjing Medical University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea |
| Interventions | ; |
A Real-World Study of Cligabalin(HSK16149) for the Treatment of Neurogenic Rosacea
Completed Trials
NCT03989492 — Role of the Sympathetic Nervous System in Rosacea
| Status | Completed |
| Phase | N/A |
| Sponsor | Kristen Metzler-Wilson |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea |
| Interventions |
Rosacea is a common skin disorder which causes facial redness and inflammation in about 16 million Americans, from an unknown cause. Many triggers of rosacea symptoms are stressors that affect the sympathetic (“fight or flight”) portion of the nervous system, and a recent pilot study suggests there is sympathetic dysfunction in rosacea. This project will benefit patients, clinicians, and basic …
NCT04472546 — Use of the SpiderMass for in Vivo Analysis of the Skin in Five Chronic Inflammatory Dermatosis
| Status | Completed |
| Phase | N/A |
| Sponsor | Pierre Fabre Dermo Cosmetique |
| Enrollment | 210 |
| Study Type | INTERVENTIONAL |
| Conditions | Acne; Atopic Dermatitis; Psoriasis Vulgaris; Rosacea; Seborrheic Dermatitis |
| Interventions | ; ; |
The physiological states of the skin are characterized by a certain homeostasis linked to the balance of the metabolic pathways. When these pathways are deregulated, the proteic, lipidic and metabolic is affected. It is thus possible to follow a change in the state of the skin by looking at change in the associated molecular profile.
The PRISM laboratory (INSERM U1192) in Lille has developed a…
NCT04275999 — Rosacea and Ivermectin
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Wake Forest University Health Sciences |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea |
| Interventions | ; ; |
The primary hypothesis is that weekly digital interactions and routine measurement of Transepidermal Water Loss (TEWL) rates and Subcutaneous hydration levels will promote patient adherence to maintenance ivermectin therapy and prevent disease relapse. The project will consist of a trial in which thirty subjects with rosacea receive ivermectin therapy and are randomized to receive either no int…
NCT04886739 — CGB-400 Topical Gel for the Treatment of Inflammatory Lesions of Rosacea
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | CAGE Bio Inc. |
| Enrollment | 78 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea |
| Interventions | ; |
This is a multicenter, randomized, double-blind, vehicle-controlled, parallel design study evaluating the efficacy and safety of CGB-400 Topical Gel for the treatment of inflammatory lesions of rosacea. The study consists of a 12-week double-blind treatment period with clinic visits at Baseline (Day 0), and Weeks 2, 4, 8, and 12.
Approximately 80 subjects will be enrolled and randomized at a 1…
NCT05045469 — Therapeutic Effects of Topical Herbal Medicine -Rhubarb Ointment on Rosacea
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Chang Gung Memorial Hospital |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea; Chinese Herbal Medicine |
| Interventions |
The aim of this study is to investigate the effects of topical herbal medicine in the patients with rosacea.
NCT05150587 — Safety, Efficacy and Pharmacokinetics of Rifaximin in Patients With Moderate-to-severe Papulopustular Rosacea
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Alfasigma S.p.A. |
| Enrollment | 216 |
| Study Type | INTERVENTIONAL |
| Conditions | Papulopustular Rosacea |
| Interventions | ; |
Rosacea is a common chronic inflammatory relapsing-remitting skin condition almost exclusively affecting the central area of the face and the eyes.
Preliminary evidence suggests that treatment with rifaximin, a poorly absorbed oral antibiotic drug may be beneficial in patients with rosacea, particularly in those with papulopustular phenotype and positivity to Lactulose Breath Test (L-BT).
The…
NCT05296629 — A Randomized, Double-Blind Study to Assess the Safety, Efficacy and Tolerability of Oral DFD-29 Capsules for the Treatment of Rosacea.
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Journey Medical Corporation |
| Enrollment | 323 |
| Study Type | INTERVENTIONAL |
| Conditions | Papulopustular Rosacea |
| Interventions | ; ; |
This is a 16-week, multicenter, randomized, parallel-group, double-blind, controlled study. After assessing eligibility during a screening period of up to 30 days, approximately 320 subjects at least 18 years old who are diagnosed with moderate to severe papulopustular rosacea will be randomized in a 3:3:2 ratio to DFD-29 (40 mg), Doxycycline capsules 40 mg, or Placebo once daily for 16 weeks.
NCT05343455 — A Study to Assess the Safety, Efficacy and Tolerability of Oral DFD-29 Capsules for the Treatment of Rosacea (MVOR-2)
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Journey Medical Corporation |
| Enrollment | 330 |
| Study Type | INTERVENTIONAL |
| Conditions | Papulopustular Rosacea |
| Interventions | ; ; |
This is a 16-week, multicenter, randomized, parallel-group, double-blind, controlled study. After assessing eligibility during a screening period of up to 30 days, approximately 320 subjects at least 18 years old who are diagnosed with moderate to severe papulopustular rosacea will be randomized in a 3:3:2 ratio to DFD-29 (40 mg), Doxycycline capsules 40 mg, or Placebo once daily for 16 weeks. …
NCT05815511 — Clinical Trial to Evaluate the Effect of a Probiotic Mixture on the Rosacea Evolution
| Status | Completed |
| Phase | N/A |
| Sponsor | Bionou Research, S.L. |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea; Rosacea Papular Type; Rosacea, Papulopustular |
| Interventions | ; |
The clinical trial has a randomized, double-blind, placebo-controlled design, in which the aim is to evaluate the effect of a probiotic mix, with a 12-week treatment, on the evolution of rosacea.
This 12 weeks of treatment are structured into three visits: Visit 1 (initial; week 0), Visit 2 (intermediate; week 6) and Visit 3 (final; week 12).
NCT06908915 — Long Pulse 1064 nm Nd:YAG Laser in the Treatment of Erythematotelangiectatic Rosacea and Other Erythematous Telangiectatic Facial Conditions
| Status | Completed |
| Phase | N/A |
| Sponsor | Hawler Medical University |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea, Erythematotelangiectatic |
| Interventions |
The goal of this clinical study is to assess the effectiveness of Nd:YAG laser 1064 nm in the long pulse mode in the treatment of signs of rosacea including the erythema of the face and telangiectasia. The used parameter of this laser was of very low energy (spot size: 5mm, fluence: 4.07 J/Cm2, energy: 800 millijoules (mJ) and frequency: 5 Hz. About 2-3 passes performed in each treatment sessio…
NCT06873087 — Changes in PACAP, CGRP, and VIP Levels in Rosacea Patients on Systemic Isotretinoin and Their Association with Erythema
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | SB Istanbul Education and Research Hospital |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea |
| Interventions |
The goal of this clinical study is to investigate the effects of systemic isotretinoin on vasoactive neuropeptides (PACAP, VIP, CGRP) and its relationship with the erythema index in patients with rosacea. It also aims to assess the clinical efficacy of isotretinoin in reducing rosacea severity. The main questions this study seeks to answer are:
Does systemic isotretinoin treatment lead to chan…
NCT06033352 — Potassium-titanyl Phosphate (KTP) Laser vs KTP Laser and Ivermectin Cream for Facial Rosacea
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Insel Gruppe AG, University Hospital Bern |
| Enrollment | 22 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea |
| Interventions | ; |
Rosacea is a frequent chronic inflammatory disease affecting mainly the face but also eyes and scalp. Rosacea is classified into 3 types: erythemato-teleangiectatica, papulopustulosa and phymatosa. Treatments depend on the type and include topical and systemic antibiotics, azelaic acid, topical ivermectin, topical brimonidine, systemic isotretinoin as well as intense pulsed light (IPL) and lase…
NCT06969300 — FMRF Combined With 30% SSA in the Treatment of Rosacea
| Status | Completed |
| Phase | N/A |
| Sponsor | Second Affiliated Hospital of Xi’an Jiaotong University |
| Enrollment | 15 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea |
| Interventions | ; |
This study was a single-center, case-by-case, bilateral facial comparison study. A total of 15 patients were included. On the day of enrollment, after the completion of the test items, treatment was carried out (full face gold micro-needling + 30% salicylic acid on the half face), and on-site follow-up was conducted 1 week later, 2 weeks later follow-up was conducted and the second acid brushin…
NCT07046039 — The Impact of Untreated Depression and Anxiety Among Patients With Skin Diseases in Jeddah, Saudi Arabia.
| Status | Completed |
| Phase | N/A |
| Sponsor | King Abdulaziz University |
| Enrollment | 215 |
| Study Type | OBSERVATIONAL |
| Conditions | Alopecia Areata; Acne Vulgaris; Psoriasis; Atopic Dermatitis (Eczema); Rosacea |
The goal of this observational study is to learn about the prevalence and severity of untreated depression and anxiety among adults with skin diseases in Jeddah, Saudi Arabia. The main question it aims to answer is:
Do patients with skin diseases experience significant levels of untreated depression and anxiety?
Participants diagnosed with skin conditions such as acne, eczema, or psoriasis co…
NCT05592548 — Rosacea Treatment Using Non-thermal (Cold) Atmospheric Plasma Device
| Status | Completed |
| Phase | N/A |
| Sponsor | The Skin Center Dermatology Group |
| Enrollment | 5 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea, Papulopustular |
| Interventions |
10-13 patients will be enrolled to receive split face treatment: the control side will be treated with metronidazole cream, the intervention side will be treated with a cold atmospheric plasma device
NCT06776445 — Efficacy and Safety of Different Dose Regimens of Gabapentin for Treating Erythema/Flushing in Rosacea: A Randomized Controlled Trial
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | First Affiliated Hospital of Chongqing Medical University |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea; Rosacea Subtype 1 (Erythematotelangiectatic) |
| Interventions | ; ; |
The goal of this clinical trial is to learn if Gabapentin works to treat flushing/erythema associated with rosacea. It will also learn about the safety of drug Gabapentin. The main questions it aims to answer are:
- Does drug Gabapentin reduce flushing and erythema associated with rosacea?
- What medical problems do participants have when taking drug Gabapentin? Researchers will compare Gabape…
NCT06557603 — Bioequivalence Study of Ivermectin 1% Cream and Soolantra (Ivermectin) 10 mg/g Cream
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | Humanis Saglık Anonim Sirketi |
| Enrollment | 44 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea |
| Interventions | ; |
Single dose bioequivalence study of Ivermectin 1% cream and Soolantra (Ivermectin) 10 mg/g cream in healthy adult human subjects.
NCT06582043 — Evaluation of the Efficacy and Tolerance of Two Cosmetic Products in Subjects With Rosacea
| Status | Completed |
| Phase | N/A |
| Sponsor | NAOS Argentina S.A. |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea; Redness; Telangiectasia; Flushing; Pustular Acne |
| Interventions | ; |
Multicentric and double-blind randomised comparative clinical study in Argentina and Brazil. Under dermatological and ophthalmological control 4 visits: inclusion [Day(D)0], D28, D56, D84 Ethical committee required.
NCT07250165 — Combined Therapy of 532-nm KTP and Microsecond 1064-nm Nd:YAG Laser for Rosacea
| Status | Completed |
| Phase | N/A |
| Sponsor | Second Affiliated Hospital, School of Medicine, Zhejiang University |
| Enrollment | 15 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea |
| Interventions |
Rosacea remains a therapeutically challenging, chronic facial dermatosis whose central feature-persistent erythema-often resists topical and systemic agents. In this study we evaluated, for the first time, the simultaneous use of a 532-nm potassium titanyl phosphate (KTP) laser and a microsecond-pulsed 1064-nm Nd:YAG laser as a safe alternative.
NCT06434519 — Metronidazole SC Penetrance With Moisturizers
| Status | Completed |
| Phase | N/A |
| Sponsor | Duke University |
| Enrollment | 21 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea, Erythematotelangiectatic |
| Interventions | ; ; |
Topical metronidazole is a widely used first line treatment for erythemotelangiectatic and inflammatory rosacea. Commonly, a moisturizer is also used to restore the skin barrier and reduce inflammation. The purpose of this study is to assess the whether the common practice of applying moisturizer prior to topical metronidazole affects this medication’s stratum corneum penetrance in rosacea pati…
NCT06915636 — Comparative Study of Low-Energy 1064nm Laser and DPL in Rosacea Treatment
| Status | Completed |
| Phase | N/A |
| Sponsor | Second Affiliated Hospital of Xi’an Jiaotong University |
| Enrollment | 31 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea |
| Interventions |
Rosacea is a common skin disease characterized by transient flushing or persistent erythema and vasodilation symptoms on the face. In more severe cases, papules and pustules may appear in the central part of the face. Rosacea can be classified into four subtypes based on clinical manifestations: erythematotelangiectatic type, papulopustular type, rhinophyma type, and ocular rosacea type. Althou…
NCT07410533 — Analysis of Factors Associated With the Efficacy of 595-nm Pulsed Dye Laser Treatment for Rosacea
| Status | Completed |
| Phase | N/A |
| Sponsor | The First Affiliated Hospital with Nanjing Medical University |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulsed Dye Laser; Rosacea |
| Interventions | ; |
This study was designed as a single-center, prospective, randomized controlled trial and included 80 patients with rosacea treated at the Department of Dermatology, Jiangsu Provincial People’s Hospital. All patients received pulsed dye laser therapy (pulsed dye laser system; Cynosure (Beijing) Medical Technology Co., Ltd., China). Treatment energy was adjusted according to individual clinical r…
NCT07431476 — Brimonidine 0.33% for Rosacea-Related Facial Erythema
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | Istanbul Training and Research Hospital |
| Enrollment | 45 |
| Study Type | INTERVENTIONAL |
| Conditions | Rosacea; Rosacea Subtype 1 (Erythematotelangiectatic) |
| Interventions | ; |
This study looks at whether a topical gel called 0.33% brimonidine can reduce persistent facial redness caused by rosacea. The study was carried out in two parts.
In the first part, the gel was applied to only one side of each participant’s face, while the other side received a placebo (a non-active gel). Redness was measured before and after application to see the immediate (short-term) effec…
Other (Withdrawn)
NCT04214483 — A Pilot Study to Explore the Role of Gut Flora in Acne
| Status | Withdrawn |
| Phase | N/A |
| Sponsor | ProgenaBiome |
| Enrollment | N/A |
| Study Type | OBSERVATIONAL |
| Conditions | Acne; Acne Vulgaris; Acne Keloidalis; Acne Keloid; Acne Conglobata |
| Interventions |
This study seeks to correlate microbiome sequencing data with information provided by patients and their medical records.
NCT03883945 — A Safety and Efficacy Study to Evaluate Rosacea
| Status | Withdrawn |
| Phase | Phase 1 / Phase 2 |
| Sponsor | AiViva BioPharma, Inc. |
| Enrollment | N/A |
| Study Type | INTERVENTIONAL |
| Conditions | Papulopustular Rosacea |
| Interventions | ; |
To evaluate the safety, efficacy, and pharmacokinetic profile of ascending concentrations of the study medication compared with vehicle in subjects with rosacea.
Other (Terminated)
NCT06013371 — PDE4 Inhibition in Seborrheic Dermatitis and Papulopustular Rosacea
| Status | Terminated |
| Phase | Phase 2 |
| Sponsor | Icahn School of Medicine at Mount Sinai |
| Enrollment | 32 |
| Study Type | INTERVENTIONAL |
| Conditions | Seborrheic Dermatitis; Papulopustular Rosacea |
| Interventions | ; |
This study is a double-blind, vehicle-controlled clinical trial. The study will take place at Icahn School of Medicine at Mount Sinai. The study will include 33-39 adult subjects with moderate-to-severe-Seborrheic dermatitis (SD) as well as 33-39 adult subjects with moderate-to-severe papulopustular rosacea (PPR). Subjects will be randomized 2:1 to receive study drug or placebo.
Enrolled subje…
NCT04731259 — Study to Evaluate the Safety of ATR-04
| Status | Withdrawn |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Azitra Inc. |
| Enrollment | N/A |
| Study Type | INTERVENTIONAL |
| Conditions | Epidermal Growth Factor; Papulopustular Rosacea |
| Interventions | ; |
This is a multicenter, randomized, double-blind, placebo-controlled phase 1b/2a study designed to evaluate the safety of an investigational product called ATR-04, to reduce the severity of epidermal growth factor receptor inhibitor (EGFRI) associated papulopustular rash on the face. This study will be performed at 10-12 clinical sites, with potentially a virtual component. Approximately 60 elig…
NCT06532136 — Deucravacitinib Rosacea
| Status | Withdrawn |
| Phase | Phase 2 |
| Sponsor | Icahn School of Medicine at Mount Sinai |
| Enrollment | N/A |
| Study Type | INTERVENTIONAL |
| Conditions | Papulopustular Rosacea |
| Interventions | ; |
This will be a double-blind, randomized placebo-controlled study in which participants will be randomized 2:1 to receive 6 mg deucravacitinib or placebo once daily for 8 weeks, followed by an open label extension during which all participants will receive 6 mg deucravacitinib once daily for an additional 8 weeks. The open-label extension has been incorporated in order to ensure all participants…