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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Trial to Test the Safety and Efficacy of TEV-53408 in Participants With VitiligoSkin and Connective Tissue Diseases, hypopigmentation of the skin, skin disorder, skin pigmentation disorder, vitiligoRecruitingPhase 12026-10-09NCT06625177
A Study of LY4005130 in Adult Participants With Non-Segmental VitiligoSkin and Connective Tissue Diseases, hypopigmentation of the skin, skin disorder, skin pigmentation disorder, vitiligoRecruitingPhase 22026-10-08NCT07533019
Analysis of Specimens From Individuals With Pulmonary FibrosisCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fibrosis, Hemic and Lymphatic Diseases, Hermansky-Pudlak syndrome, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, albinism, blood coagulation disease, blood platelet disease, eye disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, hypopigmentation of the skin, inborn disorder of amino acid metabolism, inborn errors of metabolism, inherited blood coagulation disorder, interstitial lung disease, lung disorder, metabolic disease, oculocutaneous albinism, platelet storage pool deficiency, pulmonary fibrosis, respiratory system disorder, skin disorder, skin pigmentation disorderActive, not recruitingNot stated2026-10-08NCT00084305
Clinical and Basic Investigations Into Hermansky-Pudlak SyndromeCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Eye Diseases, Hereditary, Fibrosis, Hemic and Lymphatic Diseases, Hermansky-Pudlak syndrome, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, albinism, blood coagulation disease, blood platelet disease, digestive system disorder, eye disorder, gastroenteritis, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, hypopigmentation of the skin, inborn disorder of amino acid metabolism, inborn errors of metabolism, inflammatory bowel disease, inherited blood coagulation disorder, interstitial lung disease, intestinal disorder, lung disorder, metabolic disease, oculocutaneous albinism, platelet storage pool deficiency, pulmonary fibrosis, respiratory system disorder, skin disorder, skin pigmentation disorderRecruitingNot stated2026-10-08NCT00001456
Foam Sclerotherapy With or Without Transdermal Laser for Reticular Veins and TelangiectasiasHyperpigmentation, Skin and Connective Tissue Diseases, cardiovascular disorder, skin disorder, skin pigmentation disorder, telangiectasis, vascular disorderRecruitingPhase 42026-10-05NCT07793630
Treatment and Prevention of Melasma Relapses by Using 1064nm 650 Microsecond LaserChloasma, Hyperpigmentation, Melanosis, Skin and Connective Tissue Diseases, skin disorder, skin pigmentation disorderActive, not recruitingNot applicable2026-10-01NCT06644157
Efficacy and Tolerability of a Hybrid Fractional Laser for the Treatment of Acne Scars in Patients With Skin of ColorHyperpigmentation, Hypertrophy, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, skin disorder, skin pigmentation disorderRecruitingNot applicable2026-10-01NCT05362929
Assessment of Vitiligo Lesions Using Polarized Dermoscopy, Sub-Ultraviolet Reflectance Dermoscopy, and Ultraviolet DermoscopySkin and Connective Tissue Diseases, hypopigmentation of the skin, skin disorder, skin pigmentation disorder, vitiligoRecruitingNot stated2026-09-29NCT07846969
Characterization of Bacterial and Mycosis Skin Flora in Seborrheic Macular Hypopigmentation - MicrobiomeSkin and Connective Tissue Diseases, hypopigmentation of the skin, skin disorder, skin pigmentation disorderActive, not recruitingNot applicable2026-09-29NCT06908889
A 52-Week Study to Learn About the Safety and Effects of Ritlecitinib in Participants With Nonsegmental VitiligoSkin and Connective Tissue Diseases, hypopigmentation of the skin, skin disorder, skin pigmentation disorder, vitiligoActive, not recruitingPhase 32026-09-28NCT06163326
Local Warming to Improve Pulse Oximetry Accuracy in Critically Ill PatientsCritical Illness, Disease Attributes, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, skin disorder, skin pigmentation disorderNot yet recruitingNot applicable2026-09-25NCT07792304
Skin Pigment/Pulse Oximeter in Congenital Heart Disease (CHD)Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hypoxemia, Hypoxia, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Signs and Symptoms, Respiratory, Skin and Connective Tissue Diseases, cardiovascular disorder, congenital heart disease, heart disorder, skin disorder, skin pigmentation disorderRecruitingNot stated2026-09-25NCT06575270
Fractional CO2 Laser vs Dermabrasion With 5-Fluorouracil for Acquired LeukodermaSkin and Connective Tissue Diseases, hypopigmentation of the skin, skin disorder, skin pigmentation disorder, vitiligoNot yet recruitingNot applicable2026-09-24NCT07837908
Efficacy Evaluation of a Cosmetic Product for Facial HyperpigmentationHyperpigmentation, Melanosis, Skin and Connective Tissue Diseases, skin disorder, skin pigmentation disorderRecruitingNot applicable2026-09-16NCT07769268
Topical Delgocitinib for Facial VitiligoDisease Attributes, Facies, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, hypopigmentation of the skin, skin disorder, skin pigmentation disorder, vitiligoActive, not recruitingPhase 22026-09-15NCT07820098
Vitiligo Registry for Adults and Children in the UKSkin and Connective Tissue Diseases, hypopigmentation of the skin, skin disorder, skin pigmentation disorder, vitiligoNot yet recruitingNot stated2026-09-15NCT06218082
The Pancreas Interception Center (PIC) for Early Detection, Prevention, and Novel TherapeuticsChronic Disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cronkhite-Canada syndrome, Cysts, DNA repair disease, Digestive System Diseases, Digestive System Neoplasms, Disease Attributes, Dyskinesias, Familial Atypical Multiple Mole-Melanoma, Hyperpigmentation, Lynch syndrome, Melanosis, Neoplasms by Histologic Type, Neoplasms by Site, Neurologic Manifestations, Nutritional and Metabolic Diseases, Pancreatic Cyst, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Peutz-Jeghers syndrome, Primary Immunodeficiency Diseases, Skin and Connective Tissue Diseases, Spinocerebellar Ataxias, atactic disorder, non-human animal, ataxia telangiectasia, brain disorder, cardiovascular disorder, central nervous system disorder, cerebellar ataxia, cerebellar disorder, chronic pancreatitis, classic familial adenomatous polyposis, colonic disorder, colorectal neoplasm, digestive system disorder, digestive system neoplasm, hereditary disease, hereditary neoplastic syndrome, immune system disorder, inborn error of immunity, intestinal disorder, lentigo, melanocytic neoplasm, melanocytic nevus, melanoma, cutaneous malignant, susceptibility to, 2, metabolic disease, neoplasm, nervous system disorder, neurocutaneous syndrome, pancreas disorder, pancreatic ductal adenocarcinoma, pancreatitis, skin disorder, skin pigmentation disorder, telangiectasis, vascular disorderActive, not recruitingNot stated2026-09-15NCT05692596
(Apex) Bezuclastinib in Patients With Advanced Systemic MastocytosisChronic Disease, Disease Attributes, Hemic and Lymphatic Diseases, Mast Cell Activation Disorders, Mastocytosis, Systemic, Myeloproliferative Disorders, Neoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Connective and Soft Tissue, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, Soft Tissue Neoplasms, acute myeloid leukemia, bone marrow disorder, chronic myelomonocytic leukemia, connective tissue disorder, connective tissue neoplasm, cutaneous mastocytosis, hematologic disorder, hematopoietic and lymphoid system neoplasm, immune system disorder, leukemia, maculopapular cutaneous mastocytosis, mast cell leukemia, mastocytosis, myelodysplastic/myeloproliferative disease, myeloid leukemia, neoplasm, skin disorder, skin neoplasm, skin pigmentation disorder, type III hypersensitivity diseaseRecruitingPhase 22026-09-15NCT04996875
Prospective Evaluation of Topical Almond Oil vs HydroquinonePathologic Processes, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, skin disorder, skin pigmentation disorderRecruitingPhase 42026-09-14NCT04875715
An Observational Study of Patients With Dermatologic DiseaseBacterial Infections and Mycoses, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hypersensitivity, Immediate, Infections, Skin Diseases, Eczematous, Skin and Connective Tissue Diseases, Suppuration, alopecia, alopecia areata, atopic eczema, bacterial infectious disease, dermatitis, disorder of pilosebaceous unit, hereditary disease, hereditary skin disorder, hidradenitis, hidradenitis suppurativa, hypopigmentation of the skin, hypotrichosis, immune system disorder, skin disease caused by bacterial infection, skin disorder, skin disorder caused by infection, skin pigmentation disorder, sweat gland disorder, vitiligoNot yet recruitingNot stated2026-09-10NCT07748169
A Phase IIb Dose-ranging Study to Assess the Efficacy and Safety of GIA632 in Participants With Non-segmental VitiligoSkin and Connective Tissue Diseases, hypopigmentation of the skin, skin disorder, skin pigmentation disorder, vitiligoRecruitingPhase 22026-09-09NCT07431177
Determinants of Chronic Inflammatory Skin Disease TrajectoriesBacterial Infections and Mycoses, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hypersensitivity, Immediate, Infections, Lichenoid Eruptions, Skin Diseases, Eczematous, Skin Diseases, Papulosquamous, Skin and Connective Tissue Diseases, Suppuration, alopecia, alopecia areata, atopic eczema, bacterial infectious disease, dermatitis, disorder of pilosebaceous unit, hereditary disease, hereditary skin disorder, hidradenitis, hidradenitis suppurativa, hypopigmentation of the skin, hypotrichosis, immune system disorder, lichen planus, prurigo nodularis, psoriasis, rosacea, skin disease caused by bacterial infection, skin disorder, skin disorder caused by infection, skin pigmentation disorder, sweat gland disorder, vitiligoRecruitingNot stated2026-08-28NCT05928169
Study of Chediak-Higashi SyndromeChediak-Higashi syndrome, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Hemic and Lymphatic Diseases, Infections, Nutritional and Metabolic Diseases, Primary Immunodeficiency Diseases, Skin and Connective Tissue Diseases, albinism, blood coagulation disease, blood platelet disease, eye disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, hypopigmentation of the skin, immune system disorder, inborn disorder of amino acid metabolism, inborn error of immunity, inborn errors of metabolism, leukocyte disorder, metabolic disease, phagocyte bactericidal dysfunction, platelet storage pool deficiency, skin disorder, skin pigmentation disorderRecruitingNot stated2026-08-28NCT00005917
PPDTM CorEvitasTM Vitiligo Drug Safety and Effectiveness Registry for Adults & AdolescentsSkin and Connective Tissue Diseases, hypopigmentation of the skin, skin disorder, skin pigmentation disorder, vitiligoRecruitingNot stated2026-08-26NCT07659418
Topical Metformin Versus Triple Regimen for Epidermal MelasmaHyperpigmentation, Melanosis, Skin and Connective Tissue Diseases, skin disorder, skin pigmentation disorderNot yet recruitingPhase 22026-08-21NCT07779811