ChiCTR2500110461已完成Unknown
Effect of Topical NSAIDs (Diclofenac 0.1%, Nepafenac 0.1%, Nepafenac 0.3%) on Pain Management During Intravitreal Injections: A Prospective, Non-Randomized, Case-Control Trial
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- Self-funded
- 试验地点
- 1
- 主要终点
- Mean patient-reported pain score
研究概览
简要总结
Primary objective of the study is to measure the effect of the addition of pre-operative topical NSAID on perceived pain during intravitreal injection procedures
研究设计
- 研究类型
- Interventional
- 主要目的
- 非随机对照试验
入排标准
- 年龄范围
- 18 至 —（—）
- 性别
- All
入选标准
- •Age 18 years or older;
- •Scheduled to receive a monocular intravitreal injection of an anti-VEGF agent;
- •Able to understand, consent, and use the Visual Analog Scale for pain reporting.
排除标准
- •Known hypersensitivity or allergy to proparacaine, diclofenac, nepafenac, or any other NSAID;
- •Presence of active or severe ocular surface disease (e.g., keratitis, severe dry eye);
- •History of ocular surgery within the past 3 months;
- •Concurrent use of any systemic or topical NSAIDs for any other medical reason;
- •A diagnosed anxiety disorder, severe needle phobia, or inability to comprehend the study protocol.
研究组 & 干预措施
Group 1
Group 2
Group 3
Group 4
结局指标
主要结局
Mean patient-reported pain score
时间窗: Measured once, immediately following the completion of the intravitreal injection procedure
次要结局
未报告次要终点
研究者
研究点 (1)
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