Clinical Trials on Albinism

Total 34 results





    • NCT04495218
      Not yet recruiting
      Conditions: Albinism, Ocular
    • NCT04281732
      Recruiting
      Conditions: Low Vision; Retinitis Pigmentosa; Stargardt Disease 1; Stargardt Disease 3; Stargardt Disease 4; Albinism
    • NCT04193592
      Not yet recruiting
      Conditions: Hermansky Pudlak Syndrome; Interstitial Lung Disease
    • NCT04068961
      Completed
      Conditions: Oculocutaneous Albinism; Mutation
    • NCT03959605
      Recruiting
      Conditions: Albinism, Ocular
    • NCT02872818
      Completed
      Conditions: Apoptotic Signal Pathways in Endometrial Hyperplasia
    • NCT02458417
      Completed
      Conditions: Segmental Vitiligo; Piebaldism
    • NCT02368340
      Completed
      Conditions: Hermansky Pudlak Syndrome
    • NCT02200263
      Completed
      Conditions: Ocular Albinism (OA); Oculocutaneous Albinism (OCA)
    • NCT02156427
      Completed
      Conditions: Vitiligo; Piebaldism
    • NCT01917708
      Completed
      Conditions: Hurler Syndrome; Fanconi Anemia; Glanzmann Thrombasthenia; Wiskott-Aldrich Syndrome; Chronic Granulomatous Disease; Severe Congenital Neutropenia; Leukocyte Adhesion Deficiency; Shwachman-Diamond Syndrome; Diamond-Blackfan Anemia; Dyskeratosis-congenita; Chediak-Higashi Syndrome; Severe Aplastic Anemia; Thalassemia Major; Hemophagocytic Lymphohistiocytosis; Sickle Cell Disease
    • NCT01838655
      Completed
      Conditions: Albinism; Vision Loss
    • NCT01821781
      Recruiting
      Conditions: Immune Deficiency Disorders; Severe Combined Immunodeficiency; Chronic Granulomatous Disease; X-linked Agammaglobulinemia; Wiskott-Aldrich Syndrome; Hyper-IgM; DiGeorge Syndrome; Chediak-Higashi Syndrome; Common Variable Immune Deficiency; Immune Dysregulatory Disorders; Hemophagocytic Lymphohistiocytosis; IPEX; Autoimmune Lymphoproliferative Syndrome; X-linked Lymphoproliferative Syndrome
    • NCT01663935
      Terminated
      Conditions: Albinism; Oculocutaneous Albinism
    • NCT01652092
      Recruiting
      Conditions: SCID; Omenn's Syndrome; Reticular Dysgenesis; Wiskott-Aldrich Syndrome; Bare Lymphocyte Syndrome; Common Variable Immunodeficiency; Chronic Granulomatous Disease; CD40 Ligand Deficiency; Hyper IgM Syndrome; X-linked Lymphoproliferative Disease; Hemophagocytic Lymphohistiocytosis; Griscelli Syndrome; Chediak-Higashi Syndrome; Langerhan's Cell Histiocytosis
    • NCT01640678
      Unknown status
      Conditions: Piebaldism; Segmental Vitiligo
    • NCT01417520
      Completed
      Conditions: Myelofibrosis; Gaucher Disease; Pulmonary Fibrosis; Hermansky-Pudlak Syndrome (HPS); Cancer
    • NCT01377077
      Unknown status
      Conditions: Non-segmental Vitiligo; Segmental Vitiligo; Piebaldism
    • NCT01319851
      Terminated
      Conditions: Thalassemia; Sickle Cell Disease; Glanzmann Thrombasthenia; Wiskott-Aldrich Syndrome; Chronic-granulomatous Disease; Severe Congenital Neutropenia; Leukocyte Adhesion Deficiency; Schwachman-Diamond Syndrome; Diamond-Blackfan Anemia; Fanconi Anemia; Dyskeratosis-congenita; Chediak-Higashi Syndrome; Severe Aplastic Anemia
    • NCT01176435
      Completed
      Conditions: Albinism
    • NCT00808106
      Completed
      Conditions: Oculocutaneous Albinism
    • NCT00730314
      Completed
      Conditions: Sickle Cell Disease; Thalassemia; Anemia; Granuloma; Wiskott-Aldrich Syndrome; Chediak Higashi Syndrome; Osteopetrosis; Neutropenia; Thrombocytopenia; Hurler Disease; Niemann-Pick Disease; Fucosidosis
    • NCT00514982
      Withdrawn
      Conditions: Hermanski-Pudlak Syndrome; Colitis; Cytokines; Lymphocytes; Drug Evaluation
    • NCT00467831
      Terminated
      Conditions: Hermansky-Pudlak Syndrome (HPS); Pulmonary Fibrosis; Oculocutaneous Albinism; Platelet Storage Pool Deficiency; Metabolic Disease
    • NCT00176826
      Terminated
      Conditions: Hemophagocytic Lymphohistiocytosis; X-Linked Lymphoproliferative Disorders; Chediak-Higashi Syndrome; Griscelli Syndrome; Immunologic Diseases; Langerhans-Cell Histiocytosis; Hematologic Diseases
    • NCT00176865
      Completed
      Conditions: Hemophagocytic Lymphohistiocytosis; X-Linked Lymphoproliferative Disorders; Chediak-Higashi Syndrome; Griscelli Syndrome; Immunologic Deficiency Syndromes; Langerhans-Cell Histiocytosis
    • NCT00084305
      Recruiting
      Conditions: Pulmonary Fibrosis; Healthy Volunteers; Hermansky-Pudlak Syndrome (HPS)
    • NCT00001153
      Completed
      Conditions: Albinism; Albinism, Ocular; Albinism, Oculocutaneous
    • NCT00006054
      Terminated
      Conditions: Immunologic Deficiency Syndromes; Chediak-Higashi Syndrome; Common Variable Immunodeficiency; Graft Versus Host Disease; X-Linked Lymphoproliferative Syndrome; Familial Erythrophagocytic Lymphohistiocytosis; Hemophagocytic Lymphohistiocytosis; X-linked Agammaglobulinemia; Wiskott-Aldrich Syndrome; Chronic Granulomatous Disease; X-linked Hyper IgM Syndrome; Severe Combined Immunodeficiency; Leukocyte Adhesion Deficiency Syndrome; Virus-Associated Hemophagocytic Syndrome
    • NCT00006056
      Unknown status
      Conditions: Chediak-Higashi Syndrome; Graft Versus Host Disease; X-Linked Lymphoproliferative Syndrome; Familial Erythrophagocytic Lymphohistiocytosis; Hemophagocytic Lymphohistiocytosis; Virus-Associated Hemophagocytic Syndrome
    • NCT00005933
      Completed
      Conditions: Chediak Higashi Syndrome; Chronic Granulomatous Disease; Job's Syndrome; Leukocyte Disorder
    • NCT00005917
      Recruiting
      Conditions: Chediak Higashi Syndrome
    • NCT00001456
      Recruiting
      Conditions: Hermansky-Pudlak Syndrome (HPS)
    • NCT00001596
      Completed
      Conditions: Albinism; Inborn Errors of Metabolism; Oculocutaneous Albinism; Platelet Storage Pool Deficiency; Pulmonary Fibrosis