177. Joubert syndrome related disorder [Arima syndrome (~Mar 2018)]
1 clinical trial,   1 drug   (DrugBank: 0 drug)   0 gene,   0 pathway
Searched query = "Joubert syndrome related disorder", "Arima syndrome", "Joubert syndrome and related disorder", "Joubert syndrome", "JSRD", "Senior-Loken syndrome", "Senior-Løken syndrome", "COACH syndrome", "Orofaciodigital 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.
No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | NCT00873678 (ClinicalTrials.gov) | March 2007 | 31/3/2009 | Assessment of the Prevalence of Genes AHI1, NPHP1 and CEP290 in Joubert Syndrome | Assessment of the Prevalence and Mutational Spectrum of Genes AHI1, NPHP1 and CEP290 in Joubert Syndrome and Cerebello-oculo-renal Syndromes | Joubert Syndrome;Cerebello-oculo-renal Syndromes | Biological: Whole blood sample | Assistance Publique - Hôpitaux de Paris | NULL | Completed | N/A | N/A | Both | 80 | N/A | France |