Bevacizumab Treatment For Type 1 Retinopathy of Prematurity
试验速览
- 阶段
- 2 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 77
- 试验地点
- 26
- 主要终点
- Treatment Success at 4 Weeks Post Injection
研究概览
简要总结
Type 1 retinopathy of prematurity in zone I represents the most severe type of ROP and has the worst prognosis. It is unknown whether low-dose bevacizumab will be successful in these severe cases. Also unknown is the timing and extent of peripheral retinal vascularization after low-dose bevacizumab compared with the standard dose. The current study will evaluate whether doses of 0.063 mg and 0.25mg are effective as treatment for type 1 ROP, with ROP and retinal vessels all in zone I.
详细描述
Infants with type 1 ROP and no prior treatment for ROP will be randomly assigned (1:1) to treatment with either intravitreous bevacizumab 0.063 mg or either intravitreous bevacizumab 0.25 mg. Study exams will be at 1 day, 4 days (if no improvement on day 1), 1, 2, 3, and 4 weeks, and at 2 and 4-months post-treatment (and re-treatment when indicated). Additional study exams will occur at adjusted age 6 and 12 months. Non-study examinations will be at clinician discretion and are likely to occur more often. The primary outcome will be treatment success within each dose group, defined as improvement by the day 4 exam and no recurrence of type 1 ROP or severe neovascularization requiring additional treatment within 4 weeks of injection. Important secondary outcomes include safety and efficacy. refractive outcomes, and the extent of retinal vascularization at 2 and 4 months post-injection between the two dose groups.
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
- Triple (Participant, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- — 至 6 Months（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •The study participant must have at least one eye meeting all of the inclusion criteria in order to be eligible to participate:
- •Birth weight < 1251 grams
- •Newly diagnosed (within 2 days) type 1 ROP in zone I in one or both eyes
排除标准
- •Participants meeting any of the following exclusion criteria will be excluded from study participation.
- •Previous treatment for ROP
- •Stage 4 or 5 ROP in either eye
- •Treatment could not be done within 2 days of diagnosis of type 1 ROP
- •Investigator unwilling to randomize or parent unwilling to accept randomized assignment to either treatment
- •Transfer to another hospital anticipated within the next 4 weeks where exams by study-certified examiners are not available. If hospital discharge is anticipated within the next 4 weeks, parents unable or unwilling to return to the PEDIG site for outpatient follow-up visits.
- •Active ocular infection or purulent nasolacrimal duct obstruction in either eye
- •One eye will be excluded, and other eye may be eligible, if either of the following are present:
- •Visually significant ocular anomaly (e.g., cataract, coloboma)
- •Opacity that precludes an adequate view of the retina
研究组 & 干预措施
Bevacizumab- 0.063 mg
Participants will receive a single intravitreal injection of 0.063 mg of bevacizumab in one or both eyes following enrollment into the study. The injection/s should be given as soon as possible but no later than 2 days after the diagnosis of type 1 ROP meeting all of the inclusion criteria and none of the exclusion criteria.
干预措施: Bevacizumab (Drug)
Bevacizumab- 0.25 mg
Participants will receive a single intravitreal injection of 0.25 mg of bevacizumab in one or both eyes following enrollment into the study. The injection/s should be given as soon as possible but no later than 2 days after the diagnosis of type 1 ROP meeting all of the inclusion criteria and none of the exclusion criteria.
干预措施: Bevacizumab (Drug)
结局指标
主要结局
Treatment Success at 4 Weeks Post Injection
时间窗: 4 weeks
Treatment success, determined at 4 weeks, post injection, and meeting all the following criteria: * Improvement by the 4-day exam (3 to 5 days) * No recurrence of type 1 ROP or severe neovascularization requiring additional treatment within 4 weeks of injection.
次要结局
未报告次要终点