1 enrolling by invitation, 1 unknown. 1 Not applicable.
| Phase | Trials | Status |
|---|---|---|
| Not applicable | 1 | Enrolling by invitation 1 |
Follow Chromosome 22q11.2 Deletion Syndrome: new trials by email Literature Review of Chromosome 22q11.2 Deletion Syndrome trials Research Report on Chromosome 22q11.2 Deletion 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 |
|---|---|---|---|---|---|---|
| Parent and Infant Inter(X)Action Intervention (PIXI) Parent-Infant Inter(X)action Intervention (PIXI) - Fragile X Syndrome, Angelman Syndrome | Not applicable | Enrolling by invitation | RTI International | 120 | 2018-11-30 | 2026-07-13 |
| Genetics and Psychopathology in the 22q11 Deletion Syndrome Chromosome 22q11.2 Deletion Syndrome | Unknown | UMC Utrecht | 175 | 2002-10-01 | 2006-10-13 |
DiGeorge Syndrome (2) · Angelman Syndrome (1) · Autistic Disorder (1) · Developmental Disabilities (1) · Down Syndrome (1) · Fragile X Syndrome (1) · Klinefelter Syndrome (1) · Muscular Dystrophy, Duchenne (1) · Prader-Willi Syndrome (1) · Psychotic Disorders (1) · Rett Syndrome (1) · Smith-Magenis Syndrome (1) · Telomeric 22q13 Monosomy Syndrome (1) · Tuberous Sclerosis (1) · Turner Syndrome (1)
22q11 Deletion Syndrome (2) · Abnormalities, Multiple (2) · Cardiovascular Abnormalities (2) · Cardiovascular Diseases (2) · Chromosome Disorders (2) · Congenital Abnormalities (2) · Congenital, Hereditary, and Neonatal Diseases and Abnormalities (2) · Craniofacial Abnormalities (2) · Endocrine System Diseases (2) · Genetic Diseases, Inborn (2) · Heart Defects, Congenital (2) · Heart Diseases (2) · Hemic and Lymphatic Diseases (2) · Hypoparathyroidism (2) · Lymphatic Abnormalities (2)
RTI International (1) · UMC Utrecht (1)
United States (2) · Netherlands (1)