TCTR20240330002尚未招募1 期
The study of efficacy and safety of Thai Red Cross Fibrin Glue in pterygium excision with conjunctival limbal autograft (Phase I Clinical trial)
ational Blood Centre, Thai Red Cross Society0 个研究点目标入组 10 人开始时间: 2024年3月30日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 10
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 Years 至 N/A (No limit)（—）
- 性别
- All
入选标准
- •1. Patients with primary pterygium graded as T1 or T2 for the first time, and who exhibit indications for surgery, such as pterygium causing visual impairment, eye irritation, or significant redness and inflammation; pterygium not responding to medication; minimal complications or scarring from previous pterygium excisions; and pterygium affecting the appearance or quality of life of the patient.
- •2. Patients aged 18 years or older.
- •3. Patients who consent to participate in the research and surgery and are able to follow up on treatment outcomes.
排除标准
- •1. Use of eye drops other than artificial tears or artificial tear gel.
- •2. Presence of other ocular surface diseases excluding meibomian gland dysfunction and dry eye.
- •3. Contraindications to pterygium excision and conjunctival autografting surgery, such as keratoconus or artificial cornea.
- •4. History of previous conjunctival autografting surgery.
- •5. Patients requiring simultaneous pterygium excision with other surgeries (e.g., cataract surgery).
- •6. Patients with indications for adjunctive chemotherapy (Mitomycin-C) with pterygium excision.
- •7. Pregnancy.
研究者
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