Example: Heart Attack
Clinical Trials on DiGeorge Syndrome
Total 50 results
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NCT05924347Recruiting22q11.2 Deletion Syndrome | Adolescent Idiopathic Scoliosis
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NCT05849441Not yet recruiting22Q11 Deletion Syndrome
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NCT05747456RecruitingAging | Aesthetics | Volume Deficiency in the Mid-Face
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NCT05664412Not yet recruitingtACS | 22Q11 Deletion Syndrome
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NCT05329935RecruitingComplete DiGeorge Anomaly | Complete DiGeorge Syndrome | Congenital Athymia
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NCT04639388Recruiting22q11.2 Deletion Syndrome
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NCT04463316RecruitingDisorders of Sex Development | Congenital Adrenal Hyperplasia | Tuberous Sclerosis | Kallmann Syndrome | Prader-Willi Syndrome | Neurofibromatosis | Rett Syndrome | 22q11 Deletion Syndrome | Turner Syndrome | Noonan Syndrome
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NCT04373226Recruiting22q11.2 Deletion Syndrome
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NCT03375359Recruiting
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NCT01821781RecruitingSevere Combined Immunodeficiency | Chronic Granulomatous Disease | DiGeorge Syndrome | Hemophagocytic Lymphohistiocytosis | Wiskott-Aldrich Syndrome | X-linked Lymphoproliferative Syndrome | X-linked Agammaglobulinemia | Chediak-Higashi Syndrome | IPEX | Autoimmune Lymphoproliferative Syndrome
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NCT00768820RecruitingFragile X Syndrome | Williams Syndrome | Velocardiofacial Syndrome
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NCT00556530RecruitingDiGeorge Syndrome | 22q11.2 Deletion Syndrome
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NCT03027141Enrolling by invitationDisfigurement of Face
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NCT03836300Enrolling by invitationTuberous Sclerosis | Down Syndrome | Duchenne Muscular Dystrophy | Prader-Willi Syndrome | Fragile X Syndrome | Rett Syndrome | Turner Syndrome | Williams Syndrome | Angelman Syndrome | Chromosome 22q11.2 Deletion Syndrome
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NCT05290493Active, not recruiting22q11 Deletion Syndrome
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NCT05149898Completed
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NCT04647500Completed22q11.2 Deletion Syndrome
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NCT04639960Terminated22q11.2 Deletion Syndrome
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NCT01220531Approved for marketingDiGeorge Syndrome | DiGeorge Anomaly | Complete DiGeorge Anomaly | Complete DiGeorge Syndrome
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NCT00566488CompletedDiGeorge Syndrome | Hypoparathyroidism | Complete DiGeorge Syndrome
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NCT00579709CompletedDiGeorge Syndrome | DiGeorge Anomaly | Complete DiGeorge Anomaly | Complete DiGeorge Syndrome
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NCT00849888TerminatedDiGeorge Anomaly
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NCT00576407CompletedDiGeorge Syndrome | Complete Typical DiGeorge Anomaly
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NCT00576836CompletedDiGeorge Syndrome | DiGeorge Anomaly | Complete DiGeorge Anomaly | Complete DiGeorge Syndrome
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NCT00579527CompletedDiGeorge Anomaly | Complete DiGeorge Anomaly | Complete DiGeorge Syndrome | Complete Atypical DiGeorge Anomaly | Complete Atypical DiGeorge Syndrome
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NCT02895906Completed
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NCT04141540Completed
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NCT02381457CompletedPrader-Willi Syndrome | DiGeorge Syndrome | 22q11 Deletion Syndrome | Angelman Syndrome | Trisomy 21 | Trisomy 18 | Trisomy 13 | Monosomy X | Sex Chromosome Abnormalities | 1p36 Deletion Syndrome
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NCT02890472Completed22q11 Deletion Syndrome Di George Syndrome
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NCT02430584UnknownDown Syndrome | DiGeorge Syndrome | Turner Syndrome | Klinefelter Syndrome | Edwards Syndrome | Patau Syndrome | Perinatal Infections
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NCT04470739UnknownCovid19 | Thymic Hypoplasia
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NCT02541058Completed22q.11.2 Deletion/Duplication
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NCT03284060Terminated22q11.2 Deletion Syndrome
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NCT01127503TerminatedPsychosis | Velo-cardio-facial Syndrome
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NCT00395538TerminatedDiGeorge Syndrome | Hypoparathyroidism
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NCT02787486CompletedDown Syndrome | Aneuploidy | DiGeorge Syndrome | Turner Syndrome | Klinefelter Syndrome | Chromosome Deletion | Edwards Syndrome | Patau Syndrome
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NCT00105274CompletedDiGeorge Syndrome | Velocardiofacial Syndrome | 22q11.2 Syndrome
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NCT00917189CompletedVelocardiofacial Syndrome
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NCT02460328Completed22q11.2 Deletion Syndrome | Immune Defect
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NCT01781923Completed22q11.2 Deletion Syndrome | Velo-Cardio-Facial Syndrome
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NCT01658644CompletedEffects of Photographic Aids (Photos of Faces) on Patient Recall of Their Clinical Care Team | Effects of Photographic Aids (Photos of Faces) on Clinician-patient Communication | Effects of Photographic Aids (Photos of Faces) on Overall Patient Satisfaction
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NCT02070211Unknown
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NCT00278005TerminatedDiGeorge Syndrome | Congenital Heart Defects
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NCT00784173CompletedEar Malformations in the Velocardiofacial Syndrome
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NCT00161109UnknownChromosome 22q11.2 Deletion Syndrome
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NCT00005102UnknownAbnormalities, Multiple | DiGeorge Syndrome | Chromosome Abnormalities | Conotruncal Cardiac Defects | Shprintzen Syndrome
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NCT00004351CompletedPrader-Willi Syndrome | DiGeorge Syndrome | Williams Syndrome | Angelman Syndrome | Smith-Magenis Syndrome | Chromosome Abnormalities | Shprintzen Syndrome
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NCT00004361CompletedHeart Defects, Congenital | Tetralogy of Fallot | Pulmonary Valve Stenosis | Hypoparathyroidism | Pulmonary Atresia | Conotruncal Cardiac Defects
