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临床试验/NCT03732287
NCT03732287已完成1 期

A Phase I Dose Ranging Study Evaluating the Safety and Efficacy of Cooling Anesthesia for Local Anesthesia During Intravitreal Injection (COOL 1)

Recens Medical, Inc.2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2018年11月30日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
40
试验地点
2
主要终点
Subjective Pain

研究概览

简要总结

The purpose of this clinical study is to evaluate the safety and efficacy of cooling anesthesia application to the eye as anesthesia for intravitreal injection using a novel cooling anesthesia device and determine the effects of temperature and duration of application on subjective pain after intravitreal injection.

详细描述

Intravitreal injections have become the standard of care for administering medications for retinal diseases such as age related macular degeneration and diabetic macular edema. There is considerable apprehension among patients receiving these injections, primarily revolving around adequate anesthesia during the injection. Current methods of anesthesia involve topical anesthetic drops, lidocaine gels, or subconjunctival injections of lidocaine, which suffer from either poor anesthetic effect, corneal irritation, or subconjunctival hemorrhage, as well as significant time for the onset of anesthesia.

Recens Medical has developed a novel medical device which can precisely and rapidly cool the surface of the eye This device cools to a temperature around -5 to -10 degrees Celsius, about the temperature of a cold ice cube, and thus has an excellent safety profile compared to conventional ophthalmic cryotherapy units. The value of such a device is both improved patient comfort, as well as increased efficiency and workflow for retina specialists administering intravitreal injections.

This device has been extensively tested in animal safety studies as well as pilot human studies and has not demonstrated any serious adverse effects and has shown anesthetic effects comparable to current standard of care.

This dose escalation study will test various temperatures and duration of temperatures to evaluate for safety as well as determine the optimal temperature for anesthesia during intravitreal injection.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 110 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Men and women > 18 years old at screening visit.
  • •Men and women who are undergoing intravitreal injections in either one eye or both eyes with either Lucentis or Eylea as part of their normal standard of care with a 30 gauge needle.
  • •Subject has received a minimum of 3 intravitreal injections in the study eye prior to the study visit.
  • •Subject is willing and able to sign the study written informed consent form (ICF).

排除标准

  • •History of presence of scleromalacia
  • •Preexisting conjunctival, episcleral or scleral defects
  • •Less than 18 years of age
  • •Unable to provide informed consent
  • •Has received less than 3 injections in the study eye
  • •Active severe eye disease not controlled with artificial tears and requiring Restasis or Xiidra drops.
  • •History of Endophthalmitis with intravitreal injection
  • •History of uveitis
  • •History of retinal detachment in either eye
  • •History of vitrectomy

研究组 & 干预措施

-5 degrees Celsius for 10 seconds

Experimental

干预措施: Cooling Anesthesia (Device)

-5 degrees Celsius for 20 seconds

Experimental

干预措施: Cooling Anesthesia (Device)

-10 degrees Celsius for 10 seconds

Experimental

干预措施: Cooling Anesthesia (Device)

-10 degrees Celsius for 20 seconds

Experimental

干预措施: Cooling Anesthesia (Device)

结局指标

主要结局

Subjective Pain

时间窗: 24-48 hours after injection

Pain as measured by the visual analogue scale (VAS). This was used in the previously presented SOLAR study (Clinical trials.gov, NCT01926977). Total range is 0-10, with 0 being no pain, and 10 being unbearable pain.

Number of patients with treatment adverse events as measured by slit lamp examination

时间窗: 30 minutes after injection

Full slit lamp examination of anterior and posterior segment after intravitreal injection

次要结局

  • Subject response to needle penetration(Intraoperative (During injection))
  • Time to perform intravitreal injection(Intraoperative (injection procedure))

研究者

发起方
Recens Medical, Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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