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临床试验/ACTRN12614000607673
ACTRN12614000607673尚未招募未知

Short term changes in self-reported pain measured by VAS, cervical active range of motion in all planes and pressure pain threshold at standard locally and remotely points after a posteroanterior, end-range dorsal manipulation at the more painful spinous process level (up to T7) localized by manual palpation compared with placebo in acute grade II whiplash patients (up to 3 weeks after the accident) classified following the criteria of the clinical classification of whiplash associated disorders (WAD) defined by the Quebec Task Force in 1995

niversidad de las Islas Baleares0 个研究点目标入组 60 人开始时间: 2014年6月6日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 55 Years(—)
性别
All

入选标准

  • (a) medical diagnosis of Whiplash G II (according to the Quebec Task Force); (b) age (18-55 years); (c) acute stage (<3 weeks after the motor vehicle accident)

排除标准

  • (a) have experienced a concussion during the accident ; (b) loss of consciousness due to accident; (c) loss of postural balance at the time of conducting the study; (d) cervical pain in the 3 months prior to the accident ; (e) have suffered soft tissue therapy in the 3 months prior to the study (i.e. treatment for neck pain ); (f) received shock wave therapy for any cause prior to this study; (g) history of previous whiplash; (h) history of psychological conditions (i.e.depression disorder, post -traumatic stress , ...); (i) history of neurological and / or rheumatologic and / or circulatory disorders (hypertension , heart disease or meningitis) ; (j) be affected by other physical disease that may affect the study results (i.e. fibromyalgia , ...); (k) malformations , injury or previous surgery in the cervical spine; (l) any contraindications to the spinal manipulation (i.e. tumor disease , osteitis, congenital diseases ... ); (m) be pregnant; (n) not sign the inform consent for participation in the study; (o) take any analgesic or anti-inflammatory drug and / or muscle relaxant for 48 hours prior to the study

研究者

发起方
niversidad de las Islas Baleares

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