2 recruiting, 1 completed, 1 enrolling by invitation, 1 unknown. 1 Not applicable.
| Phase | Trials | Status |
|---|---|---|
| Not applicable | 1 | Enrolling by invitation 1 |
Follow CHARGE Syndrome: new trials by email Literature Review of CHARGE Syndrome trials Research Report on CHARGE Syndrome
Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.
| Trial | Phase | Status | Sponsor | Enrollment | Start | Updated |
|---|---|---|---|---|---|---|
| Characterization and Contribution of Genome-wide DNA Methylation (DNA Methylation Episignatures) in Rare Diseases With Prenatal Onset Methylation analysis - Rare Fetal Genetic Diseases, Congenital Malformation | Recruiting | Assistance Publique - Hôpitaux de Paris | 63 | 2026-02-26 | 2026-03-27 | |
| A Strategic Approach to Safe and Effective Cochlear Implantation in Patients With CHARGE Syndrome No intervention (observational study) - CHARGE Syndrome | Completed | Seoul National University Bundang Hospital | 12 | 2025-11-21 | 2026-01-06 | |
| Palliative Care Needs of Children With Rare Diseases and Their Families Family Centered pediatric palliative care for family caregivers of children with rare diseases. - Trisomy 13 Syndrome, Arthrogryposis Congenita Multiplex With Intestinal Atresia | Not applicable | Enrolling by invitation | Children's National Research Institute | 480 | 2025-10-02 | 2026-01-28 |
| Neurovisual Function in CHARGE Syndrome visual function evaluation - CHARGE Syndrome | Unknown | Fondazione Policlinico Universitario Agostino Gemelli IRCCS | 20 | 2021-03-15 | 2023-03-13 | |
| GROWing Up With Rare GENEtic Syndromes Retrospective file studies - Prader-Willi Syndrome, PWS-like Syndrome | Recruiting | dr. Laura C. G. de Graaff-Herder | 600 | 2018-10-01 | 2023-09-06 |
Noonan Syndrome (2) · 22q11 Deletion Syndrome (1) · Acrocephalosyndactylia (1) · Adrenal Hyperplasia, Congenital (1) · Allan-Herndon-Dudley syndrome (1) · Anxiety Disorders (1) · Bardet-Biedl Syndrome (1) · Blepharophimosis syndrome Ohdo type (1) · Cockayne Syndrome (1) · Congenital Abnormalities (1) · De Lange Syndrome (1) · Depression (1) · DiGeorge Syndrome (1) · Disorder of Sex Development, 46,XY (1)
Abnormalities, Multiple (5) · Blindness (5) · Coloboma (5) · Congenital, Hereditary, and Neonatal Diseases and Abnormalities (5) · Deaf-Blind Disorders (5) · Deafness (5) · Ear Diseases (5) · Eye Diseases (5) · Eye Diseases, Hereditary (5) · Genetic Diseases, Inborn (5) · Hearing Disorders (5) · Hearing Loss (5) · Nervous System Diseases (5) · Neurologic Manifestations (5) · Otorhinolaryngologic Diseases (5)
Observation (1)
Assistance Publique - Hôpitaux de Paris (1) · Children's National Research Institute (1) · Fondazione Policlinico Universitario Agostino Gemelli IRCCS (1) · Seoul National University Bundang Hospital (1) · dr. Laura C. G. de Graaff-Herder (1)
France (1) · Italy (1) · Netherlands (1) · South Korea (1) · United States (1)
Giuseppe Zampino, medicine (1) · Maureen E Lyon, PhD (1)
R01HD117137 (1)