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临床试验/NCT04728607
NCT04728607进行中(未招募)不适用

Use of a Compression Device for Ring Removal: A Prospective Trial

Nova Scotia Health Authority1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2021年7月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
50
试验地点
1
主要终点
Number of patients with successful ring removal using a compression device

研究概览

简要总结

The usual treatment for stuck rings includes a variety of techniques including use of ice to reduce swelling, use of lubricants, and sometimes the use of string or ring cutters. The success rate of these techniques is variable and cutting the ring is usually reserved as a last resort. Sometimes removal of a ring can take time, and can cause some small injury to the patient. Because of this, it is important to consider other methods for ring removal.

This study is looking at using a device that uses compression to reduce swelling of the finger causing the ring to be stuck. This device has been approved for use in Canada. The purpose of this study is to evaluate how effective a compression device is at removing stuck rings.

The study question is: how effective is a compression device at removing stuck rings?

A Compression Device (CD) is a device that uses circumferential compression to reduce swelling around a stuck ring. The device is used by placing it near, but not over-top, the offending ring, and then is inflated compressing the finger. The device is applied, and the hand elevated, for approximately five minutes. The device is then removed, and with a small amount of lubricant, the ring is removed.

All patients requiring ring removal at the QEII emergency department, if a compression device can be used safely, will be asked if they would like to be included in the study and have their ring removal attempted by a compression device.

Following removal attempt, the clinician will document information about the ring removal. This will include some questions regarding the patient's experience with the removal. No identifying information or personal health information will be recorded.

The investigators plan to collect information about use of the compression device for a period of one year. Following this time, the data will be analyzed to determine how effective the compression device is at removing rings including statements regarding patient experience. This information will be documented in a manuscript intended for publication and may be presented at academic conferences or other continuing education events.

The investigators will be measuring the success rate of ring removal with the compression device.

In addition, the investigators will record information on any side effects of use of the compression device, as well as patient experience including pain and satisfaction.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者
是

入选标准

  • •Individuals presenting to the QEII emergency department with a chief complaint of a stuck ring on a finger, or with heath conditions that necessitate removal of a ring that cannot be removed without clinician assistance.

排除标准

  • •Contraindications to compression device use including certain bone, nerve or blood vessel conditions.

研究组 & 干预措施

Participants

Experimental

Individuals requiring ring removal.

干预措施: Compression device. (Device)

结局指标

主要结局

Number of patients with successful ring removal using a compression device

时间窗: 1 year

Successful ring removal with compression device

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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