| Detected | Trial | Change |
|---|---|---|
| 2026-08-13 | NCT00046202 Study of Inborn Errors of Cholesterol Synthesis and Related Disorders |
critical overall status: Completed → Terminated |
| 2026-08-13 | NCT00046202 Study of Inborn Errors of Cholesterol Synthesis and Related Disorders |
critical Trial terminated: Study terminated due to low enrollment and availability of alternative protocols. |
| 2026-07-29 | NCT03027440 The Developmental Origins of Suicide Mortality |
date change Primary completion pushed: 2026-07-13 -> 2027-07-13 |
| 2026-07-29 | NCT03027440 The Developmental Origins of Suicide Mortality |
date change Completion pushed: 2026-07-13 -> 2027-07-13 |
| NCT ID | Title | Condition | Status |
|---|---|---|---|
| Phase 3 | |||
| NCT06851754 | Hormone Replacement Therapy in Adolescents With Premature Ovarian Insufficiency | Premature Ovarian Insufficiency | Recruiting |
| Phase 1 | |||
| NCT00004847 | Diagnosis of Pheochromocytoma | Pheochromocytoma | Recruiting |
| Not specified | |||
| NCT03307304 | Investigations of Juvenile Neuronal Ceroid Lipofuscinosis | Juvenile Neuronal Ceroid Lipofuscinosis (CLN3) | Recruiting |
| NCT07357701 | Identifying Genome Variants in Non-Obstructive Azoospermia (NOA) or Primary Ovarian… | Primary Ovarian Insufficiency | Recruiting |
| NCT05600946 | Characterization of Dysmorphology in Subjects With Creatine Transporter Deficiency | Cognitive Disorder | Recruiting |
| NCT06749366 | Uncovering Genes Behind Cartilage Tumors and Vascular Anomalies Using Genomic Sequencing | Enchondromatosis | Recruiting |
| NCT06019182 | MEHMO Natural History and Biomarkers | Intellectual Disability | Recruiting |
| NCT02390765 | Children s Growth and Behavior Study | Obesity | Recruiting |
| NCT05031507 | Study of Skeletal Disorders | Skeletal Disorders | Recruiting |
| NCT05440617 | Biorepository in Participants Who Undergo OTC for Gonadotoxic Therapy | Acute Ovarian Failure | Recruiting |
| NCT00001595 | An Investigation of Pituitary Tumors and Related Hypothalmic Disorders | Panhypopituitarism | Recruiting |
| NCT00250159 | Natural History Study of Patients With Excess Androgen | Congenital Adrenal Hyperplasia (CAH) | Recruiting |
| NCT05047354 | Biochemical and Phenotypical Aspects of Smith-Lemli-Opitz Syndrome and Related Disorders… | Smith Lemli Opitz Syndrome | Recruiting |
| NCT04717349 | Data Collection Study of Pediatric and Adolescent Gynecology Conditions | Disorders of Sex Development (DSD) | Recruiting |
| NCT05731141 | A Prospective Natural History Study of Lymphatic Anomalies | Lymphatic Diseases | Recruiting |
| NCT07502586 | Turner Syndrome: Genetic Considerations | Genetic | Recruiting |
| NCT00344331 | Evaluation of Biochemical Markers and Clinical Investigation of Niemann-Pick Disease… | Niemann-Pick Disease, Type C | Recruiting |
| NCT02769975 | Evaluation of Children With Endocrine and Metabolic-Related Conditions | Adrenal Insufficiency | Recruiting |
| NCT03307317 | Mirror Neuron Network Dysfunction as an Early Biomarker of Neurodevelopmental Disorder | Developmental Delay | Recruiting |
| NCT03831958 | Long-Term Follow-Up of Survivors of Pediatric Cushing Disease | Cushing Disease | Recruiting |
| NCT04708431 | Androgen Receptor, Implications for Health and Wellbeing: Natural History Study of… | Androgen Insensitivity Syndrome | Recruiting |
| NCT05052216 | Development of a Wearable Point of Care Monitoring Device for Pediatric Obstructive Sleep… | Pediatric Obstructive Sleep Apnea | Recruiting |
| NCT05588167 | Establishment of Genomic and Phenotypic Database for Niemann-Pick Disease, Type C | Niemann-Pick Disease, Type C | Recruiting |
| NCT04948658 | Gonadal Tissue Freezing for Fertility Preservation in Individuals at Risk for Ovarian… | Turner Syndrome | Recruiting |
| NCT01851447 | Skeletal Muscle Biomarkers in People With Fragile Sarcolemmal Muscular Dystrophy | Genetic Disorder | Active, Not Recruiting |