Leber Hereditary Optic Neuropathy Clinical Trial
— rAAV2-ND4Official title:
Safety and Efficacy Study of a Single Intravitreal Injection of rAAV2-ND4 Treatment of Leber Hereditary Optic Neuropathy
Verified date | January 2018 |
Source | Huazhong University of Science and Technology |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study is meant to assess the safety and efficacy of rAAV2-ND4 treatment of Leber hereditary optic neuropathy with 11778 LHON mutation.
Status | Completed |
Enrollment | 9 |
Est. completion date | November 2015 |
Est. primary completion date | November 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 8 Years to 60 Years |
Eligibility |
Inclusion Criteria: 1. comply with Leber hereditary optic neuropathy diagnostic criteria. 2. in patients with informed consent, voluntary participation. 3. signed informed consent. 4. 8 = Age = 60 years old, good health, the patient can tolerate local anesthesia surgery. 5. to comply with doctor's instructions, can in the time of referral. Exclusion Criteria: 1. Cardiopulmonary and renal function in severe weakness, cancer, a variety of bleeding disorders, acute sensing disease, high fever, high fever disease, women during pregnancy, heart disease, such as post-operative recovery period. 2. Are participating in other clinical studies of patients. 3. Patients with mental disorders. |
Country | Name | City | State |
---|---|---|---|
China | Department of Ophthalmology ,Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology | Wuhan | Hubei |
Lead Sponsor | Collaborator |
---|---|
Bin Li | Huazhong University of Science and Technology |
China,
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* Note: There are 31 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The Best Corrected Visual Acuity(BCVA) | Up to 3 years | ||
Primary | Results of CD3/CD4/CD8 Test | The mean percentage of CD3+/CD4+/CD8+ test before and after treatment | up to 6 months | |
Secondary | Intraocular Pressure; | Up to 3 years | ||
Secondary | Neutralizing Antibody Assay | The mean of Neutralizing antibody assay of 8 patients before and after treatment | up to 3 years | |
Secondary | Average RNFL Thickness Througth Optical Coherence Tomography(OCT) Test | Average RNFL thickness of 8 patients througth Optical coherence tomography(OCT) test before and after treatment | Up to 3 years | |
Secondary | Computerized Visual Field(MD: Mean Deviation, the Value Close to 0 Regarded Normal) | MD: mean deviation, the value Close to 0 regarded normal.VFI/MD:The bigger one was more close to the normal value. | up to 3 years | |
Secondary | Computerized Visual Field(VFI: Visual Field Index ,the Value Close to 100% Regarded Normal) | VFI: visual field index ,the value Close to 100% regarded normal. VFI/MD:The bigger one was more close to the normal value. | up to 3 years |
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