Tuberous Sclerosis Complex: Clinical Trials

4 trials for Tuberous Sclerosis Complex, newest first

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2 unknown, 1 completed, 1 recruiting. 4 Not applicable.

By phase and status

PhaseTrialsStatus
Not applicable4Unknown 2, Completed 1, Recruiting 1

Follow Tuberous Sclerosis Complex: new trials by email Literature Review of Tuberous Sclerosis Complex trials Research Report on Tuberous Sclerosis Complex

Trials (filtered) newest first · largest first

All 4 trials

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

TrialPhaseStatusSponsorEnrollmentStartUpdated
A Smart Phone Application to Improve Adoption of the 2024 Kidney Disease Improving Global Outcomes (KDIGO) Chronic Kidney Disease (CKD) Guidelines
Use of an electronic digital Application - Chronic Kidney Disease, Proteinuria
Not applicableRecruitingSt. James's Hospital, Ireland802026-01-142026-05-01
Acceptance and Commitment Therapy in Tuberous Sclerosis Complex
Acceptance and Commitment Therapy (ACT) - Tuberous Sclerosis Complex
Not applicableUnknownUniversity Hospitals Bristol and Weston NHS Foundation Trust152021-08-122024-02-14
Early Behavioral Intervention to Improve Social Communication Function in Infants With Tuberous Sclerosis Complex
JASPER - Tuberous Sclerosis Complex
Not applicableCompletedUniversity of California, Los Angeles82015-09-012026-07-23
Long-term, Prospective Study Evaluating Clinical and Molecular Biomarkers of Epileptogenesis in a Genetic Model of Epilepsy - Tuberous Sclerosis Complex
epilepsy early diagnosis protocol - TSC, Tuberous Sclerosis Complex
Not applicableUnknownSergiusz Jozwiak1002013-11-012014-04-04

Narrower conditions

Tuberous Sclerosis (4)  ·  Epilepsy (1)  ·  Kidney Diseases (1)  ·  Nephrotic Syndrome (1)  ·  Proteinuria (1)  ·  Psychological Well-Being (1)  ·  Renal Insufficiency, Chronic (1)

Broader conditions

Congenital Abnormalities (4)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (4)  ·  Genetic Diseases, Inborn (4)  ·  Hamartoma (4)  ·  Heredodegenerative Disorders, Nervous System (4)  ·  Malformations of Cortical Development (4)  ·  Malformations of Cortical Development, Group I (4)  ·  Neoplasms (4)  ·  Neoplasms, Multiple Primary (4)  ·  Neoplastic Syndromes, Hereditary (4)  ·  Nervous System Diseases (4)  ·  Nervous System Malformations (4)  ·  Neurocutaneous Syndromes (4)  ·  Neurodegenerative Diseases (4)  ·  Behavior (1)

Interventions

Acceptance and Commitment Therapy (1)  ·  Activator Appliances (1)

Sponsors

Sergiusz Jozwiak (1)  ·  St. James's Hospital, Ireland (1)  ·  University Hospitals Bristol and Weston NHS Foundation Trust (1)  ·  University of California, Los Angeles (1)

Countries

Austria (1)  ·  Belgium (1)  ·  Czechia (1)  ·  France (1)  ·  Germany (1)  ·  Ireland (1)  ·  Italy (1)  ·  Netherlands (1)  ·  Poland (1)  ·  United Kingdom (1)  ·  United States (1)

Top investigators

Donal Sexton, MB BCh BAO BSc, MRCPI, MD, PhD (1)  ·  Sam Amin, MBCHB MSc PhD (1)  ·  Seriusz Jozwiak, Md, PhD (1)  ·  Shafali Jeste, MD (1)  ·  Susan McAnallen, MB BCh BAO, MRCPI, ESENeph (1)

Results publications

PMID 31912454, PMID 39625912