Keratoderma, Palmoplantar
Keratoderma, Palmoplantar
Explore linked clinical trials. Standard reference: MESH:M00119748 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Epidermal Growth Factor Receptor Inhibition for Keratinopathies | Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Ichthyosiform Erythroderma, Congenital, Infant, Newborn, Diseases, Keratoderma, Palmoplantar, Skin Abnormalities, Skin and Connective Tissue Diseases, ectodermal dysplasia syndrome, epidermolytic ichthyosis, hereditary disease, hereditary skin disorder, ichthyosis, keratosis, nail disorder, pachyonychia congenita, skin disorder | Not yet recruiting | Phase 1 / Phase 2 | 2026-08-03 | NCT06545695 | |
| Study to Evaluate the Safety and Efficacy of Tapinarof in Adults With Palmoplantar Keratoderma | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Keratoderma, Palmoplantar, Skin and Connective Tissue Diseases, hereditary disease, hereditary skin disorder, keratosis, skin disorder | Active, not recruiting | Phase 2 | 2026-06-23 | NCT06561321 | |
| Instrumental Assessment of Plantar Hyperkeratosis in Healthy Subjects and Patients With Diabetes | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Keratoderma, Palmoplantar, Keratoderma, Palmoplantar, Diffuse, Keratoderma, Palmoplantar, Epidermolytic, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, diabetes mellitus, endocrine system disorder, glucose metabolism disease, hereditary disease, hereditary skin disorder, keratosis, metabolic disease, skin disorder | Not yet recruiting | Not applicable | 2026-02-17 | NCT07412561 | |
| FARD (RaDiCo Cohort) (RaDiCo-FARD) | Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Conjunctival Diseases, Eye Diseases, Hereditary, Infant, Newborn, Diseases, Keratoderma, Palmoplantar, Neoplasms by Histologic Type, Neoplasms, Nerve Tissue, Nutritional and Metabolic Diseases, Pemphigoid, Benign Mucous Membrane, Skin Abnormalities, Skin and Connective Tissue Diseases, albinism, autoimmune disease, ectodermal dysplasia syndrome, eye disorder, hereditary disease, hereditary neoplastic syndrome, hereditary skin disorder, hypopigmentation of the skin, ichthyosis, immune system disorder, inborn disorder of amino acid metabolism, inborn errors of metabolism, incontinentia pigmenti, inherited epidermolysis bullosa, inherited neurodegenerative disorder, keratosis, metabolic disease, mucous membrane pemphigoid, neoplasm, nerve sheath neoplasm, nervous system disorder, neurocutaneous syndrome, neurodegenerative disease, neurofibroma, neurofibromatosis, neurofibromatosis type 1, neuromuscular disease, pemphigus, peripheral nervous system disorder, skin disorder, skin pigmentation disorder, vesiculobullous skin disease | Recruiting | Not stated | 2026-02-12 | NCT05954416 | |
| Qualitative Study in Patients With Genodermatoses and Healthcare Professionals on Reproductive Counselling | Abnormalities, Multiple, Bone Diseases, Developmental, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cysts, Eye Diseases, Hereditary, Infant, Newborn, Diseases, Jaw Cysts, Jaw Diseases, Keratoderma, Palmoplantar, Malformations of Cortical Development, Group I, Neoplasms by Histologic Type, Neoplasms, Multiple Primary, Nutritional and Metabolic Diseases, Skin Abnormalities, Skin and Connective Tissue Diseases, Stomatognathic Diseases, albinism, basal cell carcinoma, basal cell neoplasm, bone disorder, carcinoma, central nervous system malformation, cerebral cortical dysplasia, connective tissue disorder, cutis laxa, ectodermal dysplasia syndrome, epidermolysis bullosa, epithelial neoplasm, eye disorder, hamartoma, hereditary disease, hereditary neoplastic syndrome, hereditary skin disorder, hypopigmentation of the skin, ichthyosis, inborn disorder of amino acid metabolism, inborn errors of metabolism, inherited neurodegenerative disorder, keratosis, metabolic disease, musculoskeletal system disorder, neoplasm, nervous system disorder, neurocutaneous syndrome, neurodegenerative disease, nevoid basal cell carcinoma syndrome, odontogenic cyst, skin disorder, skin pigmentation disorder, solitary bone cyst, tuberous sclerosis, vesiculobullous skin disease | Recruiting | Not stated | 2025-05-18 | NCT06330350 | |
| Reproductive Options in Inherited Skin Diseases | Abnormalities, Multiple, Bone Diseases, Developmental, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cysts, DNA repair disease, Eye Diseases, Hereditary, Infant, Newborn, Diseases, Jaw Cysts, Jaw Diseases, Keratoderma, Palmoplantar, Malformations of Cortical Development, Group I, Neoplasms by Histologic Type, Neoplasms, Multiple Primary, Nutritional and Metabolic Diseases, Skin Abnormalities, Skin and Connective Tissue Diseases, Stomatognathic Diseases, albinism, basal cell carcinoma, basal cell neoplasm, bone disorder, carcinoma, central nervous system malformation, cerebral cortical dysplasia, connective tissue disorder, cutis laxa, ectodermal dysplasia syndrome, epidermolysis bullosa, epithelial neoplasm, eye disorder, hamartoma, hereditary disease, hereditary neoplastic syndrome, hereditary skin disorder, hypopigmentation of the skin, ichthyosis, inborn disorder of amino acid metabolism, inborn errors of metabolism, inherited neurodegenerative disorder, keratosis, metabolic disease, musculoskeletal system disorder, neoplasm, nervous system disorder, neurocutaneous syndrome, neurodegenerative disease, nevoid basal cell carcinoma syndrome, odontogenic cyst, photosensitivity disease, precancerous condition, skin disorder, skin pigmentation disorder, solitary bone cyst, tuberous sclerosis, vesiculobullous skin disease, xeroderma pigmentosum | Enrolling by invitation | Not stated | 2025-05-18 | NCT06330324 | |
| Evaluation of Oral Potentially Malignant Disorders (OPMDs) with STRATICYTE™ | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Erythroplasia, Keratoderma, Palmoplantar, Keratoderma, Palmoplantar, Diffuse, Keratoderma, Palmoplantar, Epidermolytic, Pathologic Processes, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, Stomatognathic Diseases, disease, hereditary disease, hereditary skin disorder, hyperplasia, keratosis, leukoplakia, mouth disorder, neoplasm, precancerous condition, skin disorder | Recruiting | Not stated | 2024-11-07 | NCT05853783 | |
| Early Prediction of Oral Cancer by S100A7 Immunohistochemistry Signature-based Assessment | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Erythroplasia, Head and Neck Neoplasms, Keratoderma, Palmoplantar, Keratoderma, Palmoplantar, Diffuse, Keratoderma, Palmoplantar, Epidermolytic, Mouth Neoplasms, Neoplasms by Histologic Type, Neoplasms by Site, Pathologic Processes, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, Stomatognathic Diseases, carcinoma, disease, epithelial neoplasm, head and neck squamous cell carcinoma, hereditary disease, hereditary skin disorder, hyperplasia, keratosis, leukoplakia, mouth disorder, neoplasm, precancerous condition, skin disorder, squamous cell carcinoma | Recruiting | Not stated | 2024-11-07 | NCT04622462 |