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Condition(s)/Problem(s)

  •   Congenital malformations, deformations and chromosomal abnormalities
Condition(s)/Problem(s)
No.Overall StatusScientific Title
        15 Not yet recruiting Phase 3, Open-Label, Single-Arm Study to Evaluate the Efficacy and Safety of PF-07055480 (Recombinant AAV2/6 Human Factor VIII Gene Therapy) in Adult Male Participants with Moderately Severe to Severe Hemophilia A (FVIII:C≤1%)
First subject enrolled prior to CRIS registration 14 Recruiting Genetic identification of hereditary cystic kidney diseases for implementing precision medicine
First subject enrolled prior to CRIS registration 13 Completed A 8 week, multi-center, randomized, double-blind, placebo-controlled clinical trial for the evaluation of the efficacy and safety of MAEC on gingival health
First subject enrolled prior to CRIS registration 12 Recruiting Determining the ideal insertion depth of ultrasound guided right subclavian vein catheter in pediatric patients by anatomic landmarks
First subject enrolled prior to CRIS registration 11 Completed Registration and sample collection for identification of genetic and public health characteristics of the major birth defects in korea
        10 Not yet recruiting Perioperative changes of muscle mass measured by ultrasound in pediatric patients with congenital heart defects and the impact of sarcopenia on postoperative outcomes: prospective observational study
        9 Not yet recruiting Analysis of characteristics in electroencephalography according to age and general anesthetics in children undergoing congenital heart surgery
First subject enrolled prior to CRIS registration 8 Completed The effects of GJB2 mutation on language skill in Cochlear Implantation
First subject enrolled prior to CRIS registration 7 Recruiting A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Trial of Tadalafil for Duchenne Muscular Dystrophy
First subject enrolled prior to CRIS registration 6 Recruiting Multicenter and dose escalation phase 1 study to evaluate the safety and exploratory efficacy of GC1119 (recombinant human α-galactosidase A) for enzyme replacement therapy in Fabry disease patients
  •    12   마지막으로이동