A Prospective, Single-Center, Randomized, Double Blind, Double Arm, Comparative Clinical Trial to Compare the Safety and Preliminary Efficacy Between Ranibizumab Monotherapy and Ranibizumab Combined With R:GEN (Selective Retina Therapy) in Clinically Significant Diabetic Macular Edema (a Pilot Study)
试验速览
- 阶段
- 4 期
- 入组人数
- 12
- 试验地点
- 1
- 主要终点
- Best Corrected Visual Acuity (BCVA) change in the study group
研究概览
简要总结
The objective of this clinical trial is to compare and evaluate the safety and efficacy of Ranibizumab (Lucentis®; Novartis AG, Basel, Switzerland) monotherapy and Ranibizumab combined with R:GEN (Selective Retina Therapy) in patients with clinically significant diabetic macular edema.
详细描述
This is a prospective, single-center, randomized, double blind, double arm, comparative clinical trial to compare the safety and efficacy between ranibizumab monotherapy and ranibizumab combined with Selective Retina Therapy (SRT) in clinically significant diabetic macular edema (a pilot study).
Screening visit should be conducted within 30 days before the baseline visit. After assigning a screening number (SN) to the participants who voluntarily agreed in writing to participate in the clinical trial, conduct a screening test to determine whether the subject meet the inclusion/ exclusion criteria.
Proceed with the clinical trial with the appropriate subjects determined based on the inclusion/exclusion criteria. Random allocation numbers (AN) are assigned.
Participants are randomly assigned to study group or control group. Combination therapy of SRT and ranibizumab is performed in the study group and sham SRT and ranibizumab monotherapy is performed in the control group. (Sham) SRT and ranibizumab (re-performance) is performed by the institution's investigator other than the independent evaluator.
In the study group and control group, after the completion of 5 ranibizumab injections during the loading period, if the independent evaluator judges the following criteria apply based on Best Corrected Visual Acuity (BCVA) and Optical Coherence Tomography (OCT) findings at each visit from the 5th month, ranibizumab is re-administered by an investigator other than the independent evaluator, within 14 days of the visit or on the day of visit; If the independent evaluator judges that CMT on the OCT is equal to or greater than the baseline; or if the independent evaluator judges that BCVA is equal to or worse than the baseline.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Outcomes Assessor)
盲法说明
The participant must be masked from the information on the treatment group assignment.
The BCVA and image (OCT, Color Fundus Photography (CFP), Fundus Autofluorescence (FAF), Fluorescence Angiography (FAG)) investigator of the institution must be blinded on the participants' treatment group assignment to eliminate bias in evaluation.
Based on the images (OCT, CFP, FAF) and quantified measurement results (BCVA, OCT), the blinded principal investigator (independent evaluator) evaluates efficacy and adverse events and determines whether ranibizumab should be administered again.
An investigator not blinded performs SRT and ranibizumab administration.
入排标准
- 年龄范围
- 19 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adults older than 19 years of age
- •Patients with Type-I or Type-II diabetes
- •Patients diagnosed with Clinically Significant Diabetic macular edema (CSME) based on the criteria of Early Treatment Diabetic Retinopathy Study (ETDRS).
- •If thickened retina is within or lies on the circle with a radius of 500µm from the center of the fovea, or
- •If the hard exudate is within or lies on the circle with a radius of 500 ㎛ and if the retina adjacent to it is thickened, or
- •If there is a thickened retina larger than 1 disc area and if a part of it is over the circle with a radius of 1 disc diameter from the center of the macula.
- •Central Macular Thickness (CMT) of study eye is more than 300㎛ on OCT
- •Patients with BCVA of the study eye between 20/320 and 20/
- •Patients who have agreed to participate in this study and signed the consent form, and patients whose legally acceptable representative signed the consent form
排除标准
- •Patients with Ischemic DME that showed rupture in the Foveal Avascular Zone due to the obstruction of more than 30% of the capillary vessels in the central circle, as observed using fluorescein angiography
- •Patients with a history of focal steroid treatment in the study eye within 4 months
- •Patients with a history of anti-VEGF agent injection in the study eye within 3 months
- •Patients with rubeosis iridis, vitreous hemorrhage or tractional retinal detachment in the study eye
- •Patients with uncontrolled glaucoma in the study eye
- •Patients with active inflammation or infection in the study eye (in or around the eye)
- •Patients with disorders in the study eye that may confuse interpretation of the clinical trial results, cause severe visual loss, and require medical or surgical intervention during the study, based on the investigator's judgment (media opacity such as corneal opacity, cataract, and vitreous opacity, vitreous macular traction, uveitis, macular atrophy, macular degeneration, choroidal neovascularization, retinal vascular occlusion)
- •Persons with a history of treatment with anti-VEGF drugs within the past 6 months, or if they anticipate future use (e.g.: sorafenib (Nexavar®), sunitinib (Sutent®), bevacizumab (Avastin®))
- •Persons with confirmed allergy to fluorescein, indocyanine green or iodine
- •Patients with a clinically significant disorder such as uncontrolled renal failure that would make it difficult for them to participate in this study, based on the investigator's judgment
- •Pregnant or lactating woman
- •Patient not using contraception or with a possibility of pregnancy during the clinical trial period
- •Other persons deemed to be difficult to participate in this study, based on the investigator's judgment
- •Persons participating in a study other than observational or non-interventional study
研究组 & 干预措施
Selective Retina Therapy and ranibizumab combination therapy
Perform R:GEN laser (SRT) on the 6,000 microns diameter region including macular edema, while excluding the 500 microns diameter region from the fovea, with the appropriate treatment energy determined.
Ranibizumab (Lucentis®; Novartis AG, Basel, Switzerland) injection into the vitreous cavity at 3.5-4.0 mm posterior to the corneal limbus, towards the center of the eye, avoiding horizontal meridians. Then, 0.05 mL of the injection solution is slowly injected.
In study group and the control group, ranibizumab is administered 5 times in total from the baseline to month 4.
干预措施: R:GEN laser treatment (Selective Retina Therapy) and Lucentis (ranibizumab) combination therapy (Combination Product)
Sham Selective Retina Therapy and ranibizumab monotherapy
For the participants assigned to the control group, sham procedures are performed in Sham Mode. All procedures except for the absence of laser light emission at the laser irradiation stage are the same with the study group.
Sham SRT is performed three times in total, one time for each visit for month 1, 3, and 5. At the time of month 1 and 3, Sham SRT should be performed before administration of ranibizumab.
干预措施: R:GEN laser treatment (Selective Retina Therapy) and Lucentis (ranibizumab) combination therapy (Combination Product)
结局指标
主要结局
Best Corrected Visual Acuity (BCVA) change in the study group
时间窗: 12 months
Compare BCVA change evaluated between the group where Ranibizumab was combined with R:GEN (Selective Retina Therapy) and the group where Ranibizumab monotherapy was applied
次要结局
- Central Macular Thickness (CMT) change in the study group(12, 24 months)
- Maximum Macular Thickness (MMT) change in the study group(12, 24 months)
- Best Corrected Visual Acuity (BCVA) change in the study group(12, 24 months)
- Rate and number of Ranibizumab re-performance in the study group(24 months)
- Adverse Event analysis(24 months)