EUCTR2013-005464-25-FR进行中(未招募)不适用
Assessment of Anatomical and Functional Outcomes in Patients Treated with Ocriplasmin for Vitreomacular Traction/Symptomatic Vitreomacular Adhesion (VMT/sVMA) - Ocriplasmin for Vitreomacular Traction/Symptomatic Vitreomacular Adhesion
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 入组人数
- 474
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •- Ages Eligible for Study: 18 Years and older
- •- Genders Eligible for Study: Both
- •- Diagnosis of vitreomacular traction/symptomatic vitreomacular adhesion (VMT/sVMA), with evidence of focal VMT visible on Spectral Domain Optical
- •Coherence Tomography (SD-OCT).
- •- Read, sign, and date an Institutional Review Board/Ethics Committee-approved informed consent form.
- •- Other protocol-defined inclusion criteria may apply.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 142
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 332
排除标准
- •- Women of childbearing potential if pregnant, breastfeeding, or not in agreement to use adequate birth control methods to prevent pregnancy throughout the study.
- •- Hypersensitivity to ocriplasmin or any of the Jetrea excipients
- •- Active or suspected intraocular or periocular infection
- •- Presence of Epiretinal Membrane (ERM) over the macula at baseline
- •- Broad VMT/VMA >1500 microns at Baseline
- •- History of vitrectomy in the study eye
- •- History of laser photocoagulation to the macula in the study eye
- •- Any relevant concomitant ocular condition that, in the opinion of the investigator, could be expected to worsen or require surgical intervention during the study period
- •- Macular hole of >400µm diameter in the study eye
- •- High myopia in study eye
- •- Pseudo-exfoliation, Marfan’s syndrome, phacodonesis or any other finding in the Investigator’s opinion suggesting lens/zonular instability.
- •- Therapy with another investigational agent within 30 days prior to Visit 1.
- •- Active, simultaneous enrollment in another ophthalmology clinical study.
- •- Other protocol-defined exclusion criteria may apply
研究者
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已完成
4 期
Assessment of Anatomical and Functional Outcomes in Patients Treated with Ocriplasmin for Vitreomacular Traction/Symptomatic Vitreomacular Adhesion (VMT/sVMA)Vitreomacular traction10047060NL-OMON40974Alcon Laboratories50
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