Feasibility Study and Preliminary Application Study on Iris OCTA
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| ClinicalTrials.gov Identifier: NCT03631108 |
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Recruitment Status : Unknown
Verified September 2018 by Shanghai Eye Disease Prevention and Treatment Center.
Recruitment status was: Not yet recruiting
First Posted : August 15, 2018
Last Update Posted : September 6, 2018
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| Condition or disease | Intervention/treatment |
|---|---|
| Conjunctivitis Glaucoma Myopia Diabetic Retinopathy Retinal Detachment Retinal Neovascularization, Unspecified Uveitis | Diagnostic Test: OCTA (ZEISS) |
- Feasibility study of iris OCTA technology
- Establishment of iris OCTA database in normal population and analysis of related factors: (1) different sex; (2) different age; (3) different myopic diopter; (4) 24-hour diurnal changes from morning to night; (5) before and after mydriasis; (6) different blood pressure; (7) different intraocular pressure; (8) different blood glucose; (9) before and after exercise. (10) drinking water, tea, coffee and red wine.
- Analysis of iris OCTA data related to eye diseases:(1) conjunctivitis; (2) glaucoma; (3) childhood myopia; (4) uveitis; (5) diabetic retinopathy; (6) retinal detachment; (7) fundus neovascularization.
- Influence of commonly used ophthalmic drops on iris OCTA data. Observe the difference of iris OCTA test data before and after treatment: (1) conjunctivitis treated with levofloxacin antibiotics; (2) glaucoma treated with prostaglandins, adrenalines and receptor blockers; (3) childhood myopia treated with atropine drugs (4) uveitis treated with hormonal drugs. (5) diabetic retinopathy treated with vasodilator.
- Effect on iris OCTA data before and after ophthalmic surgery. (1) cataract, phacoemulsification + intraocular lens implantation; (2) glaucoma, iridectomy; (3) fundus neovascularization, intraocular injection of anti-VEGF; (4) diabetic retinopathy, vitreous surgery.
| Study Type : | Observational |
| Estimated Enrollment : | 4000 participants |
| Observational Model: | Case-Control |
| Time Perspective: | Cross-Sectional |
| Official Title: | Feasibility Study and Preliminary Application Study on Noninvasive Iris Optical Coherence Tomography Angiography (OCTA) |
| Estimated Study Start Date : | October 2018 |
| Estimated Primary Completion Date : | April 2019 |
| Estimated Study Completion Date : | June 2019 |
| Group/Cohort | Intervention/treatment |
|---|---|
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Normal Population
Normal population with different gender, different age different, different blood pressure, different ocular pressure, etc. All participants will underwent imaging using the OCTA system (Zeiss) with the anterior segment optical adaptor lens. |
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Patients with common ophthalmic diseases
(1) conjunctivitis; (2) glaucoma; (3) childhood myopia; (4) uveitis; (5) diabetic retinopathy; (6) retinal detachment; (7) fundus neovascularization. All patients will underwent imaging using the OCTA system (Zeiss) with the anterior segment optical adaptor lens. |
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Patients using eye drops
(1) conjunctivitis patients treated with levofloxacin antibiotics; (2) glaucoma patients treated with prostaglandins, adrenaline or receptor blockers drugs; (3) childhood myopia patients treated with atropine drugs; (4) uveitis patients treated with hormones treatment. (5) diabetic retinopathy patients treated with vasodilator. All patients will underwent imaging using the OCTA system (Zeiss) with the anterior segment optical adaptor lens before and after eyedrops. |
Diagnostic Test: OCTA (ZEISS)
All participants will underwent imaging using the OCTA system (Zeiss) with the anterior segment optical adaptor lens. |
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Ocular surgery patients
(1) cataract, phacoemulsification + intraocular lens implantation; (2) glaucoma, iridectomy; (3) fundus neovascularization, intraocular injection of anti-VEGF; (4) diabetic retinopathy, vitrectomy. All patients will underwent imaging using the OCTA system (Zeiss) with the anterior segment optical adaptor lens before and after surgery. |
Diagnostic Test: OCTA (ZEISS)
All participants will underwent imaging using the OCTA system (Zeiss) with the anterior segment optical adaptor lens. |
- Iris Vessel Geometric Characteristics [ Time Frame: 0:00 8:00 14:00 20:00 ]Iris vascular density and neovascular density
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| Ages Eligible for Study: | Child, Adult, Older Adult |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Healthy volunteers and ophthalmological patients who can understand and agree to cooperate this study will be included.
Exclusion Criteria:
- Patients who can not cooperate with the examination.
| Responsible Party: | Shanghai Eye Disease Prevention and Treatment Center |
| ClinicalTrials.gov Identifier: | NCT03631108 |
| Other Study ID Numbers: |
2018KY181 |
| First Posted: | August 15, 2018 Key Record Dates |
| Last Update Posted: | September 6, 2018 |
| Last Verified: | September 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Undecided |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Iris Vessel OCTA |
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Diabetic Retinopathy Uveitis Conjunctivitis Retinal Detachment Retinal Neovascularization Neovascularization, Pathologic Eye Diseases Retinal Diseases Diabetic Angiopathies |
Vascular Diseases Cardiovascular Diseases Diabetes Complications Diabetes Mellitus Endocrine System Diseases Uveal Diseases Metaplasia Pathologic Processes Conjunctival Diseases |

