central diabetes insipidus
Information
- Disease name
- central diabetes insipidus
- Disease ID
- DOID:0081055
- Description
- "A diabetes insipidus that is characterized by polyuria and polydipsia due to a deficiency in vasopressin synthesis." [url:https\://pubmed.ncbi.nlm.nih.gov/15070970/]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT01280188 | Completed | Phase 3 | A Study of Minirin Melt in Japanese Patients With Central Diabetes Insipidus (CDI). | January 2011 | August 2012 |
| NCT04902235 | Completed | Phase 4 | Identification and Clinical Relevance of an Oxytocin Deficient State (CRH Study) | July 6, 2021 | May 1, 2023 |
| NCT05319301 | Completed | N/A | Identification and Clinical Relevance of an Oxytocin Deficient State (Melatonin Study) | April 1, 2022 | November 1, 2023 |
| NCT04789148 | Not yet recruiting | Phase 1 | Effects of Intranasal Oxytocin in Patients With Central Diabetes Insipidus | June 2023 | June 30, 2025 |
| NCT03474601 | Recruiting | Seoul National University Pituitary Disease Cohort Study | March 15, 2015 | February 14, 2025 | |
| NCT04897802 | Recruiting | Phase 4 | Identification and Clinical Relevance of an Oxytocin Deficient State (GLP1 Study) | September 13, 2021 | December 31, 2024 |
- Disase is a (Disease Ontology)
- DOID:9409
- Cross Reference ID (Disease Ontology)
- GARD:6015
- Cross Reference ID (Disease Ontology)
- ORDO:178029
- HPO alt_id (Human Phenotype Ontology)
- HP:0008210
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0000863
- OrphaNumber from OrphaNet (Orphanet)
- 178029