Genetic testing ( DrugBank: - )
3 diseases
| 告示番号 | 疾患名（ページ内リンク） | 臨床試験数 |
|---|---|---|
| 6 | パーキンソン病 | 3 |
| 90 | 網膜色素変性症 | 1 |
| 299 | 嚢胞性線維症 | 1 |
6. パーキンソン病
臨床試験数 : 2,307 / 薬物数 : 2,007 - (DrugBank : 349) / 標的遺伝子数 : 188 - 標的パスウェイ数 : 199
| 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 | NCT04919356 (ClinicalTrials.gov) | June 8, 2021 | 4/6/2021 | Parkinson's Disease G2019S LRRK2 Genetic Testing Program | G2019S LRRK2 Parkinson's Disease: Increasing Awareness and Genetic Testing Program | Parkinson's Disease | Genetic: G2019S LRRK2 | Escape Bio, Inc. | Engage Health Inc.;Sano | Terminated | 18 Years | N/A | All | 836 | United States | |
| 2 | NCT03279445 (ClinicalTrials.gov) | August 9, 2017 | 14/8/2017 | Parkinson's Disease in African American and Caucasian Patients | Characteristics of African American People With Parkinson's Disease: A Hospital Based Study at the University of Chicago of the African American Community in Chicago's South Side | Parkinson Disease | Genetic: Genetic testing | University of Chicago | NULL | Recruiting | 15 Years | 100 Years | All | 600 | United States | |
| 3 | NCT02668835 (ClinicalTrials.gov) | November 2015 | 4/12/2015 | GADGET-PD Genetic and Digital Diagnosis of Essential Tremor and Parkinson's Disease Trial | GADGET-PD Genetic and Digital Diagnosis of Essential Tremor and Parkinson's Disease Trial | Parkinson Disease;Essential Tremor | Device: Non intervention-Monitoring device;Genetic: Non intervention-Genetic testing | Scripps Translational Science Institute | Michael J. Fox Foundation for Parkinson's Research;Intel Corporation | Completed | 18 Years | N/A | All | 67 | NULL |
90. 網膜色素変性症
臨床試験数 : 147 / 薬物数 : 176 - (DrugBank : 43) / 標的遺伝子数 : 49 - 標的パスウェイ数 : 110
| 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 | NCT02309866 (ClinicalTrials.gov) | January 2015 | 24/11/2014 | Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases | Retinitis Pigmentosa | Genetic: Genetic testing | Hillel Yaffe Medical Center | Technion, Israel Institute of Technology | Not yet recruiting | N/A | N/A | Both | 100 | N/A | NULL |
299. 嚢胞性線維症
臨床試験数 : 1,695 / 薬物数 : 1,527 - (DrugBank : 268) / 標的遺伝子数 : 111 - 標的パスウェイ数 : 174
| 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 | NCT05599958 (ClinicalTrials.gov) | October 10, 2022 | 20/10/2022 | Clinical and Genetic Profile of Pediatric Patients With Cystic Fibrosis in Sohag. | Clinical and Genetic Profile of Pediatric Patients With Cystic Fibrosis in Sohag. | Cystic Fibrosis | Diagnostic Test: sweat chloride test;Genetic: genetic testing | Sohag University | NULL | Recruiting | 2 Days | 18 Years | All | 15 | Egypt |