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临床试验/NCT04136197
NCT04136197已完成不适用

The Determination of the Trigger Point Incidence After Lumbar Disc Herniation Surgery

Istanbul University - Cerrahpasa (IUC)1 个研究点 分布在 1 个国家目标入组 110 人开始时间: 2020年7月18日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
110
试验地点
1
主要终点
Manual Palpation

研究概览

简要总结

Our purpose is to determine the incidence of trigger points in patients who remain in a fixed position for a long time during lumbar disc herniation surgery.

详细描述

The 110 participants between 30-70 years are chosen from patients who had lumbar disc herniation surgery. The trigger points are determined by manually palpating quadratus lumborum, iliocostalis lumborum, gluteus Maximus, gluteus minimus, gluteus medius, ve piriformis muscles before and after surgery. Data will be recorded on the patient assessment file and transferred to the computer and analyzed. Data analysis will be performed with SPSS.20.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
30 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • To be between 30-70 years
  • To have low back pain during minimum 6 weeks
  • To be voluntary participation for this study
  • To approve the informed consent form
  • To have the trigger point causing low back pain on muscles including quadratus lumborum, iliocostalis lumborum, gluteus maximus, gluteus minimus, gluteus medius, ve piriformis muscles.

排除标准

  • To be diagnosed with spinal stenosis or spondylolisthesis
  • To have any skin problem affecting lower extremity evaluation
  • To have tumor on spinal region
  • To have rheumatological or any systemic problem that may interfere with trigger point diagnose

结局指标

主要结局

Manual Palpation

时间窗: Change from baseline (preoperative state) to postoperative first and third day

The patients are positioned in a sitting and prone lying posture.Trigger points are discrete, local, hypersensitive spots located in a taut band of muscles. Palpation of the trigger point will cause elicitation pain over the affected area and radiation of pain toward a zone of reference and a local twitch response.

Visual Analog Scale

时间窗: Change from baseline (preoperative state) to postoperative first and third day

Pain will be assessed with Visual Analog Scale (VAS).The VAS is usually a horizontal line, 10 cm in length, anchored by word descriptors at each end with "No Pain" (score of zero) on the left side up to "pain as bad as it could be" or the "worst imaginable pain" (Score of 100 \[100-mm scale\]) on the right side.The patient was asked to mark the line point that represented his or her current pain.

次要结局

未报告次要终点

研究者

发起方
Istanbul University - Cerrahpasa (IUC)
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ebru Kaya Mutlu, PT

Associate Prof. Dr, PhD

Istanbul University - Cerrahpasa (IUC)

研究点 (1)

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