pseudohypoparathyroidism
pseudohypoparathyroidism
Explore linked clinical trials. Standard reference: MONDO:001999211 results · Page 1 of 1
Clinical trials
Swipe the table sideways for more columns.
| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| German Hypoparathyroidism Registry | Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, bone disorder, calcium metabolic disease, endocrine system disorder, hereditary disease, hypoparathyroidism, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease, musculoskeletal system disorder, parathyroid gland disorder, pseudohypoparathyroidism | Recruiting | Not stated | 2026-10-05 | NCT07857460 | |
| Natural History Study of Parathyroid Disorders | Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Head and Neck Neoplasms, Neoplasms by Site, Neoplasms, Multiple Primary, Nutritional and Metabolic Diseases, Parathyroid Neoplasms, bone disorder, calcium metabolic disease, endocrine system disorder, hereditary disease, hereditary neoplastic syndrome, hyperparathyroidism, inborn errors of metabolism, inborn metal metabolism disorder, malignant endocrine neoplasm, metabolic disease, multiple endocrine neoplasia, multiple endocrine neoplasia type 1, musculoskeletal system disorder, neoplasm, parathyroid gland disorder, primary hyperparathyroidism, pseudohypoparathyroidism | Recruiting | Not stated | 2026-09-17 | NCT04969926 | |
| Theophylline for Treatment of Pseudohypoparathyroidism | Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, bone disorder, calcium metabolic disease, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease, musculoskeletal system disorder, pseudohypoparathyroidism, pseudohypoparathyroidism type 1A | Enrolling by invitation | Phase 2 | 2026-09-02 | NCT04240821 | |
| Theophylline Treatment for Pseudohypoparathyroidism | Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, bone disorder, calcium metabolic disease, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease, musculoskeletal system disorder, pseudohypoparathyroidism | Active, not recruiting | Phase 2 | 2026-09-02 | NCT03029429 | |
| Setmelanotide to Treat Obesity in a Patient With Pseudohypoparathyroidism Type 1a (PHP1a) | Body Weight, Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Overweight, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, bone disorder, calcium metabolic disease, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease, musculoskeletal system disorder, nutritional disorder, obesity disorder, overnutrition, pseudohypoparathyroidism, pseudohypoparathyroidism type 1A | Enrolling by invitation | Phase 2 | 2026-07-23 | NCT07496463 | |
| Albright Hereditary Osteodystrophy: Natural History, Growth, and Cognitive/Behavioral Assessments | Bone Diseases, Developmental, Bone Diseases, Endocrine, Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dwarfism, Nutritional and Metabolic Diseases, bone disorder, brain disorder, calcium metabolic disease, central nervous system disorder, endocrine system disorder, hereditary disease, hypopituitarism, hypothalamic disorder, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease, musculoskeletal system disorder, nervous system disorder, pituitary dwarfism, pituitary gland disorder, pseudohypoparathyroidism, pseudohypoparathyroidism type 1A, pseudopseudohypoparathyroidism | Active, not recruiting | Not applicable | 2026-06-02 | NCT00209235 | |
| Theophylline Treatment for Pseudohypoparathyroidism - Children 2-12 Years Old | Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, bone disorder, calcium metabolic disease, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease, musculoskeletal system disorder, pseudohypoparathyroidism, pseudohypoparathyroidism type 1A | Active, not recruiting | Phase 2 | 2026-04-29 | NCT04551170 | |
| IDMet (RaDiCo Cohort) (RaDiCo-IDMet) | Abnormalities, Multiple, Angelman syndrome, Beckwith-Wiedemann syndrome, Bone Diseases, Metabolic, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Dwarfism, Imprinting Disorders, Musculoskeletal Abnormalities, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, Overweight, Prader-Willi syndrome, Silver-Russell syndrome, Temple syndrome, bone disorder, calcium metabolic disease, central nervous system disorder, chromosomal disorder, endocrine system disorder, gonadal disorder, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, intellectual disability, metabolic disease, movement disorder, multiple congenital anomalies due to 14q32.2 maternally expressed gene defect, musculoskeletal system disorder, nervous system disorder, nutritional disorder, obesity disorder, overnutrition, paternal uniparental disomy of chromosome 14, precocious puberty, pseudohypoparathyroidism, transient neonatal diabetes mellitus | Recruiting | Not stated | 2026-02-12 | NCT05945576 | |
| Tunisian Clinical Registry on Hypoparathyroidism and Pseudo-hypoparathyroidism | Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, bone disorder, calcium metabolic disease, endocrine system disorder, hereditary disease, hypoparathyroidism, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease, musculoskeletal system disorder, parathyroid gland disorder, pseudohypoparathyroidism | Not yet recruiting | Not stated | 2025-02-21 | NCT06445036 | |
| Institution of an Italian Multicenter Database of Patients Affected by Hypoparathyroidism or Pseudohypoparathyroidism | Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, bone disorder, calcium metabolic disease, endocrine system disorder, hereditary disease, hypoparathyroidism, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease, musculoskeletal system disorder, parathyroid gland disorder, pseudohypoparathyroidism | Recruiting | Not stated | 2025-01-23 | NCT06645899 | |
| Effect of Theophylline in Pseudohypoparathyroidism | Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Pseudohypoparathyroidism, Type Ia, bone disorder, calcium metabolic disease, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease, musculoskeletal system disorder, pseudohypoparathyroidism, pseudohypoparathyroidism type 1C | Recruiting | Phase 4 | 2022-07-22 | NCT03718403 |