310. 先天異常症候群 [臨床試験数:10,薬物数:18(DrugBank:10),標的遺伝子数:3,標的パスウェイ数:7

Searched query = "Congenital anomalies syndrome", "Trisomy 1q", "9q34 deletion syndrome", "Cornelia de Lange syndrome", "CdLS", "Smith-Lemli-Opitz syndrome", "SLO syndrome"
The queries were searched in Public_title, Scientific_title, and Condition. Export date: 03/15/2021. Trials are sorted by Date_enrollment from most recent to oldest in the table.

Search in Page e.g. "Phase 3", "Not recruiting", "Japan"
1 trial found
No.TrialIDDate_
enrollment
Date_
registration
Public_titleScientific_titleConditionInterventionPrimary_
sponsor
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sponsor
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Status
Inclusion_
agemin
Inclusion_
agemax
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PhaseCountries
1ChiCTR20000354772020-08-112020-08-12Clinical study on the diagnosis of Smith Lemli Opitz syndrome by GC-MSClinical study on the diagnosis of Smith Lemli Opitz syndrome by GC-MS Smith-Lemli-Opitz syndromeGold Standard:Quantitative detection of 7-DHC;Index test:Detection of chol and 7-DHC in clinical samples by GC-MS;Obstetrics and Gynecology Hospital Affiliated to Fudan UniversityNULLPending01BothTarget condition:110;Difficult condition:0China