跳至主要内容
临床试验/CTRI/2024/07/070574
CTRI/2024/07/070574尚未招募不适用

Comparison of Surgical outcome in endoscopic dacryocystorhinostomy with and without silicone stent: Hospital based study

Dr Mukesh Verma1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年7月25日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
To observe the patency of lacrimal sac after endosopic DCR with silicone stent and without stent

研究概览

简要总结

This study is prospective, non randomized, comparative study after approval of institutional Ethical Committee in patients satisfying inclusion criteria planned for endoscopic dacryocystorhinostomy. Material used will be silicone stent, endoscope (30 and 0 degree), Topical anaesthetic agent (LIgnocaine 4% with Adrenaline 1:10,000), Tilleys forcep, Freers elevator, Suction tip, Antifog solution(savlon). The study population will be divided into 2 groups of 30 each. One group will have silicone stent placed in nasolacrimal sac. In the second group, no stent will be placed after Endo DCR. Patency and synechiae formation will be assessed at 1, 3, 6 ,10weeks and 6month. Other complications will also be assessed

研究设计

研究类型
Interventional
分配方式
Na
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • Patients with chronic dacryocystitis.
  • Age more than 18 years.

排除标准

  • Patient not giving consent Age less than 18 years Revision cases of endoscopic DCR suspicion of malignancy.

结局指标

主要结局

To observe the patency of lacrimal sac after endosopic DCR with silicone stent and without stent

时间窗: 1week, 3 week, 6 week and 10 week and 6month

次要结局

  • Observe synechiae formation after and other complication of endoscopic DCR with silicone stent and without stent(1week, 3 week, 6 week and 10 week and 6month)

研究者

发起方
Dr Mukesh Verma
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Mukesh Verma

Government Medical College, Haldwani

研究点 (1)

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