Aortic Stenosis, Supravalvular: Clinical Trials

36 trials for Aortic Stenosis, Supravalvular, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

18 completed, 8 recruiting, 3 not yet recruiting, 3 unknown. 10 Not applicable, 3 Phase 2, 2 Phase 4.

By phase and status

PhaseTrialsStatus
Not applicable10Completed 4, Recruiting 2, Unknown 2, Enrolling by invitation 1, Not yet recruiting 1
Phase 23Completed 2, Active not recruiting 1
Phase 42Completed 1, Recruiting 1

Follow Aortic Stenosis, Supravalvular: new trials by email Literature Review of Aortic Stenosis, Supravalvular trials Research Report on Aortic Stenosis, Supravalvular

Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
A Clinical Trial to Evaluate the Effects of the NeuEve Dryness Treatment Kit on Vaginal Health, Comfort, and Quality of Life in Postmenopausal Women
Intervention - Relieves Vaginal Dryness / Improves Self-Lubrication, Improves Strength & Elasticity of Vagina (Aka Collagen and Elastin)
Not applicableNot yet recruitingNeuEve402026-09-012026-10-26
A Case-Control Observational Study of Peripheral Blood-Derived iPSC Models to Investigate Oligodendrocyte Lineage Development in Children With Williams Syndrome and Healthy Controls
one-time peripheral blood collection - Williams Syndrome, Induced Pluripotent Stem Cell (Ips Cell)
Not yet recruitingQilu Hospital of Shandong University62026-04-012026-04-17
Research on the Molecular Mechanism of Cognitive Differences Between Williams Syndrome and Autism Spectrum Disorder
Williams Syndrome, Autism Disorder
Not yet recruitingQilu Hospital of Shandong University752026-04-012026-04-03
Intensive Multimodal Neurorehabilitation Targeting Neuroplasticity in Pediatric Neurodevelopmental and Chromosomal Disorders
Neurodevelopmental Disorders, Neurodevelopmental Disorders (NDD)
RecruitingHealing Hope International1002026-03-012026-03-25
Physical Activity and Community EmPOWERment Project
PACE Program - Intellectual Disability, Neurodevelopmental Disorders
Not applicableRecruitingUniversity of North Carolina, Chapel Hill3762025-01-102026-02-23
Characterization and Natural History of Williams Syndrome and Other Chromosome 7q11.23 Variants
Williams Beuren Syndrome, Williams Syndrome
RecruitingUniversity of Pennsylvania20002024-10-212026-06-08
Phonological Constraints on Language Development in Individuals With Williams Syndrome
EEG-NIRS protocol, Questionnaire - Williams Syndrome, Language
Not applicableRecruitingCentre Hospitalier Universitaire, Amiens1302024-07-052025-12-16
Clemastine Treatment in Individuals With Williams Syndrome
Open Label Clemastine with a blinded randomize withdrawal - Williams Syndrome
Phase 2Active not recruitingSheba Medical Center302024-04-012026-03-06
Clemastine Fumarate in the Treatment of Neurodevelopmental Delays in Williams Syndrome
Clemastine Fumarate Tablets, corn starch tablets - Williams Syndrome, Child
Phase 2CompletedQilu Hospital of Shandong University282024-03-202026-03-19
Motor Deficits and Signal Conduction in Individuals With Williams Syndrome
Williams Syndrome
WithdrawnSheba Medical Center2023-02-012024-06-25
Buspirone Treatment of Anxiety in Williams Syndrome
Buspirone - Williams Syndrome, Anxiety
Phase 4CompletedMassachusetts General Hospital202021-08-012024-12-03
Gene First Approach to Connective Tissue Disease
Abnormal Elastogenesis, Vascular Diseases
CompletedNational Heart, Lung, and Blood Institute (NHLBI)322021-04-222026-08-07
Quantification of Elastin Markers Synthesis in Williams-Beuren Syndrome and 7q11.23 Micro-duplication Syndrome
Physical examination and Urine and blood samples, Urine and blood samples - Williams-Beuren Syndrome, Micro-duplication 7q11.23 Syndrome
Not applicableUnknownHospices Civils de Lyon902019-10-012019-08-12
Cognitive and Behavioral Therapy of Anxiety in Williams Syndrome
Cognitive and Behavioral Therapy - Williams Syndrome, Anxiety
UnknownUniversity Hospital, Montpellier52019-08-292019-10-18
Comparison of Spectral Photon Counting CT (SPCCT) With Dual Energy CT (DECT) and Magnetic Resonance Imaging (MRI) for Plaque and Lumen Carotid Arteries Evaluation
Spectral Photon Counting Computed Tomography (SPCCT), Dual Energy CT (DECT) - Supra-Aortic Stenosis
Not applicableCompletedHospices Civils de Lyon222019-06-202024-07-15
Parent and Infant Inter(X)Action Intervention (PIXI)
Parent-Infant Inter(X)action Intervention (PIXI) - Fragile X Syndrome, Angelman Syndrome
Not applicableEnrolling by invitationRTI International1202018-11-302026-07-13
Early Check: Expanded Screening in Newborns
Confirmatory Testing - Spinal Muscular Atrophy, Fragile X Syndrome
Active not recruitingRTI International300002018-10-152026-07-01
GROWing Up With Rare GENEtic Syndromes
Retrospective file studies - Prader-Willi Syndrome, PWS-like Syndrome
Recruitingdr. Laura C. G. de Graaff-Herder6002018-10-012023-09-06
Williams Syndrome Strength, Hormones, Activity & Adiposity, DNA Programming, Eating Study
Williams Syndrome, Lipedema
CompletedMassachusetts General Hospital1442018-10-012023-10-19
Broad Band Light for the Treatment and Prevention of Senile Purpura
Broad Band Light (BBL) - Senile Purpura, Bateman's Purpura
Not applicableCompletedSiperstein Dermatology102018-08-272021-04-13

Showing 20 of 36. Sign in to see all of them.

Narrower conditions

Williams Syndrome (29)  ·  Fragile X Syndrome (6)  ·  DiGeorge Syndrome (5)  ·  Prader-Willi Syndrome (5)  ·  Autism Spectrum Disorder (4)  ·  Angelman Syndrome (3)  ·  Cardiovascular Diseases (3)  ·  De Lange Syndrome (3)  ·  Down Syndrome (3)  ·  Rare Diseases (3)  ·  Rett Syndrome (3)  ·  Anxiety Disorders (2)  ·  Ataxia with vitamin E deficiency (2)  ·  Autistic Disorder (2)

Broader conditions

Aortic Valve Disease (36)  ·  Aortic Valve Stenosis (36)  ·  Heart Diseases (36)  ·  Heart Valve Diseases (36)  ·  Cardiovascular Diseases (33)  ·  Chromosome Disorders (30)  ·  Congenital Abnormalities (30)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (30)  ·  Nervous System Diseases (30)  ·  Neurobehavioral Manifestations (30)  ·  Genetic Diseases, Inborn (28)  ·  Intellectual Disability (28)  ·  Neurologic Manifestations (28)  ·  Pathological Conditions, Signs and Symptoms (13)

Interventions

Blood Specimen Collection (1)  ·  Buspirone (1)  ·  Clemastine (1)  ·  Cognitive Behavioral Therapy (1)  ·  Exome Sequencing (1)  ·  Fluoxetine (1)  ·  Methods (1)  ·  Methylphenidate (1)  ·  Minoxidil (1)  ·  Restraint, Physical (1)  ·  Risperidone (1)  ·  Starch (1)  ·  Surveys and Questionnaires (1)  ·  Urination (1)  ·  Vitamin D (1)

Sponsors

Hospices Civils de Lyon (4)  ·  National Heart, Lung, and Blood Institute (NHLBI) (4)  ·  Massachusetts General Hospital (3)  ·  Qilu Hospital of Shandong University (3)  ·  RTI International (2)  ·  Sheba Medical Center (2)  ·  Bambino Gesù Hospital and Research Institute (1)  ·  Centre Hospitalier Universitaire, Amiens (1)  ·  Healing Hope International (1)  ·  Hôpital le Vinatier (1)  ·  National Center for Research Resources (NCRR) (1)  ·  National Institute of Mental Health (NIMH) (1)  ·  National Institute of Neurological Disorders and Stroke (NINDS) (1)  ·  NeuEve (1)  ·  Sanford Health (1)

Countries

United States (20)  ·  France (6)  ·  Israel (3)  ·  China (2)  ·  Finland (1)  ·  Italy (1)  ·  Netherlands (1)

Top investigators

Manfred Boehm, M.D. (4)  ·  Anne Wheeler, PhD (1)  ·  Benjamin Yerys, PhD (1)  ·  Bonita P Klein-Tasman, Ph.D. (1)  ·  Brianne R Tomaszewski, PhD., MPH (1)  ·  Carolyn Mervis, PhD (1)  ·  Curt Scharfe, MD, PhD (1)  ·  Daniel Rader, MD (1)  ·  Dr. Tina Casoglos-Adamopoulos, OT, OTD, BCP (1)  ·  Edward Brodkin, MD (1)  ·  James R. Lupski (1)  ·  Karen F Berman, M.D. (1)  ·  Massimiliano Rossi, MD (1)

Results publications

PMID 29614955, PMID 31138170, PMID 31315600, PMID 33667672, PMID 35142618, PMID 36752464, PMID 37010888, PMID 37633900

NIH funding

R01AG076678 (1)