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临床试验/NCT05596448
NCT05596448进行中(未招募)不适用

Investigation of the Efficiency of Coccygeal Nerve Radiofrequency Treatment in Coccydynia'

Diskapi Teaching and Research Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年10月22日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
60
试验地点
1
主要终点
Paris Functional Coccydynia Questionnaire

研究概览

简要总结

Coccydynia or coccygeal pain is a painful syndrome that affects the coccyx region. The most important etiological factors in the formation of coccidynia are; external and internal trauma. Patients with coccydynia typically complain of coccyx pain. This pain increases with prolonged sitting, bending backwards during sitting, standing for long periods of time, and standing up after sitting. Conservative treatments such as nonsteroidal anti-inflammatory drugs (NSAIDs), levator sudden relaxation exercises, seat cushions, and transcutaneous electrical simulation have all been used to relieve pain, but these methods are ineffective in 10% of patients. In the patient group unresponsive to conservative treatments, there are various interventional treatment options, including caudal epidural steroid injection, ganglion impar blocks, radiofrequency ablation of the sacral nerves, block of the coccygeal nerves and radiofrequency ablation, and coccygectomy.

详细描述

In algoloji clinic, routinely apply ultrasound-guided coccygeal nerve block and radiofrequency ablation to patients with coccydynia. During the procedure, after imaging the sacral and coccygeal corns with ultrasonography, a radiofrequency ablation needle is inserted at the level of the coccygeal horn and radiofrequency ablation is applied at 90 degrees for 60 seconds. Patients are followed for a while in our post-procedure service for possible hypotension and allergic reactions. In this study, it was planned to apply the Visual Pain Scale (VAS) and Paris Functional Coccydynia Questionnaire at the 1st week, 1st month and 3rd months after the treatment to patients who had coccygeal nerve block and radiofrequency ablation in our clinic due to the complaint of coccydynia resistant to conservative treatment methods. In this way, it is planned to evaluate the efficacy of treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Coccygeal pain

排除标准

  • Malignancy
  • İnfection
  • Coagulation disorders

结局指标

主要结局

Paris Functional Coccydynia Questionnaire

时间窗: 4 weeks

It is a scale that measures the severity of coccygeal pain. Scored between ''0: no pain'' and ''10: worst pain.

次要结局

  • Visual analog scale (VAS)(4 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Damla Yürük

Principal Investigator

Diskapi Teaching and Research Hospital

研究点 (1)

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