EUCTR2010-023037-35-GB进行中(未招募)不适用
Short-term intraocular pressure trends in high risk patients following intravitreal Ranibizumab (Lucentis) injections for Wet Age Related Macular Degeneration - Is there a role for systemic Acetazolamide (Diamox) in those with glaucoma? - LIEPS - Lucentis Injection Eye Pressure Study
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
- 24
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
- •The sample group will include glaucoma and glaucoma suspect patients undergoing intravitreal injections for neovascular (wet) AMD at York Hospital.
- •1.Patients with neovascular (wet) AMD requiring Lucentis injections
- •2.Glaucoma or Glaucoma suspect
- •3.Written informed consent
- •4. Baseline pre injection Intraocular Pressure of less than 30 mmHg
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 0
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 24
排除标准
- •1.Baseline pre-injection IOP of 30 mmHg or higher
- •2.Unable to give written informed consent
- •3.Known allergy to sulphur containing drugs or acetazolamide
- •4. 18 years or younger
- •5. Marked kidney or liver disease/dysfunction
- •6. Supra-renal gland failure
- •7. Hypercholrcmic adcidosis
- •8. Hepatic cirrhosis
- •9. Pregnancy and pre-menopausal women
- •10. Concomitant use of other oral carbonic anhydrase inhibitors apart from acetazolamide
研究者
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