Clinical Trials on Genetic Diseases
Total 381884 results
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Novo Nordisk A/SCompletedNoonan Syndrome | Genetic DisorderSweden
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Goldman, Butterwick, Fitzpatrick and GroffGalderma R&DNot yet recruitingSkin LaxityUnited States
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University of Texas Southwestern Medical CenterCompleted
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BTL Industries Ltd.Completed
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Apyx MedicalCompletedLax SkinUnited States
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Cynosure, Inc.CompletedSkin LaxityUnited States
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Northwestern UniversityWithdrawn
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R2 DermatologyCompleted
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Venus ConceptCompleted
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Ulthera, IncCompleted
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Ulthera, IncCompleted
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Ulthera, IncTerminatedSkin LaxityUnited States
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Ospedale San RaffaeleRecruitingGenetic Predisposition to Disease | Salt; Excess | Hypertension,Essential | Genetic HypertensionItaly
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National Cancer Institute (NCI)Completed
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Ankara UniversityActive, not recruitingSudden Infant DeathTurkey
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Fondation Ophtalmologique Adolphe de RothschildInstitut National de la Santé Et de la Recherche Médicale, FranceTerminated
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Edimer PharmaceuticalsCompletedEctodermal DysplasiaUnited States
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University of AberdeenRecruitingTakotsubo CardiomyopathyUnited Kingdom
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Galderma Brasil Ltda.Recruiting
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Goldman, Butterwick, Fitzpatrick and GroffSofwave Medical LTDRecruitingSkin LaxityUnited States
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InMode MD Ltd.CompletedSkin LaxityUnited States
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Apyx MedicalCompleted
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Botanee Group Co., Ltd.Completed
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Apyx MedicalActive, not recruiting
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BTL Industries Ltd.Completed
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University of Texas Southwestern Medical CenterCompleted
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Recros Medica, Inc.UnknownSkin LaxityUnited States
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Ulthera, IncCompleted
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Ulthera, IncCompleted
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Ulthera, IncCompleted
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Ulthera, IncCompleted
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Ulthera, IncCompletedSkin LaxityUnited States
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TESS Research FoundationStanford UniversityEnrolling by invitationEpilepsy | Movement Disorders | Rare Diseases | Genetic Disorder | Citrate Transporter Deficiency | SLC13A5 Deficiency | EIEE25 | Kohlschutter-Tonz Syndrome (Non-ROGDI) | 17p13.1 Deletions Confined to SLC13A5 Gene | Citrate Transporter DisorderUnited States
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University of UlsterDSM Nutritional Products, Inc.UnknownParticipants With the MTHFR 677TT GenotypeUnited Kingdom
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Hugo W. Moser Research Institute at Kennedy Krieger...RecruitingLeukoencephalopathies | Genetic Disease | White Matter Disease | Ataxia, Cerebellar | LBSL | Leukoencephalopathy With Brainstem and Spinal Cord Involvement and Lactate ElevationUnited States
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National Institute of Allergy and Infectious Diseases...RecruitingPrimary Immune DeficiencyUnited States, Turkey
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CHU de ReimsUnknownBullous PemphigoidFrance
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McMaster UniversityUniversity of Manitoba; St. Joseph's Healthcare Hamilton; University of British... and other collaboratorsUnknownAsthma in Children | Environmental Exposure | Genetic Predisposition | Allergy in Children
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University of HelsinkiUnknownCoronary Disease | InflammationFinland
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Amway (China) R&D CenterRecruiting
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Shenzhen Precision Health Food Technology Co. Ltd...Not yet recruitingSkin Laxity | Skin FoldChina
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Oslo University HospitalCompleted
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Northwestern UniversityAnn & Robert H Lurie Children's Hospital of ChicagoCompleted
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Ulthera, IncCompletedSkin Laxity | Skin CrepinessUnited States
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Cairo UniversityCompletedGastrostomy | Skin LaxityEgypt
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Novo Nordisk A/SCompletedPrader-Willi Syndrome | Genetic DisorderGermany, Denmark, Switzerland
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Novo Nordisk A/SCompletedNoonan Syndrome | Genetic DisorderSweden
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NightstaRx Ltd, a Biogen CompanyCompletedChoroideremiaFinland, United States, Canada, Denmark, Netherlands, Germany, United Kingdom, Brazil, France