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Showing trials with last updates posted in 2026.

NCT06226051 | RECRUITING
120 participants

Growing Little PEAPODS Study

Study Type:
OBSERVATIONAL
Last Updated:
2026-08-19
Start Date:
2024-09-04
Completion:
2028-01-31
Conditions
  • Premature Birth
  • Premature Infant
  • Premature
  • Intrauterine Growth Restriction
  • Small for Gestational Age at Delivery
Interventions
  • DEVICE
No Results Yet
NCT06092346 | RECRUITING
999 participants

A Natural History Study Seeks to Understand the Clinical, Genomic, Pharmacological, Laboratory, and Dietary Determinates of Pyrimidine and Purine Metabolism Disorders

Study Type:
OBSERVATIONAL
Last Updated:
2026-08-19
Start Date:
2023-12-19
Completion:
2099-01-01
Conditions
  • AMPD3, OMIM*102772, AMP Deaminase Deficiency
  • AK1, OMIM *103000, Adenylate Kinase Deficiency
  • AMPD1, OMIM *102770, Myopathy Due to Myoadenylate Deaminase Deficiency
  • TPMT, OMIM *187680, Thoipurines, Poor Metabolism of
  • IMPDH1, OMIM *146690, Retinitis Pigmentosa Type 10, Leber Congenital Amauriosis Type 11
  • APRT, OMIM *102600, Adenine Phosphoribosyltransferase Deficiency
  • HPRT1, OMIM *308000 Lesch-Nyhan Disease
  • XDH, OMIM *607633, Xanthinuria Type 1
  • SLC2A9, OMIM *606142 Hypouricemia
  • SLC22A12, OMIM *607096 Hypouricemia
  • PRPS1 Def, OMIM *311850, Arts Syndrome; Charcot-Marie-Tooth Disease
  • PRPS1 SA, OMIM *311850 Gout, PRPS-related Phosphoribosylpyrophosphate Synthetase Superactivity
  • AMPD2, OMIM *102771, Spastic Paraplegia 63; Pontocerebellar Hypoplasia
  • ITPA, OMIM *147520, Inosine Triphosphatase Deficiency; Developmental and Epileptic Encephalopathy 35
  • ADSL, OMIM *608222, Adenylosuccinate Lyase Deficiency
  • PNP, OMIM *164050, Nucleoside Phosphorylase Deficiency
  • ADA2, OMIM *607575,Sneddon Syndrome; VAIHS
  • CAD, *1140120, Developmental and Epileptic Encephalopathy
  • UPB1, OMIM *606673, Beta-ureidopropionase Deficiency
  • DPYS, OMIM *613326, Dihydropyrimidinase Deficiency
  • DPYD, OMIM *274270, Dihydropyrimidine Dehydrogenase Deficiency
  • DHODH, OMIM *126064, Miller Syndrome (Postaxial Acrofacial Dysostosis)
  • UMPS, OMIM *613891, Orotic Aciduria
  • NT5C3A<TAB>, OMIM *606224, Anemia, Hemolytic, Due to UMPH1 Deficiency
  • UNG, OMIM *191525, Hyper-IgM Syndrome 5
  • AICDA, OMIM *605257, Immunodeficiency With Hyper-IgM, Type 2; HIGM2
  • Purine-Pyrimidine Metabolism
  • Metabolic Disease
No Results Yet
NCT06044675 | RECRUITING | PHASE2
60 participants

MDMA-Assisted CBCT for PTSD vs CBCT RCT

Study Type:
INTERVENTIONAL
Last Updated:
2026-08-19
Start Date:
2024-11-15
Completion:
2027-03-31
Conditions
  • Post Traumatic Stress Disorder
Interventions
  • DRUG
  • BEHAVIORAL
No Results Yet
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