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
相似试验
已完成
不适用
Immediate changes in pain thresholds, lumbopelvic mobility and posture in functional chronic constipation patients after a visceral manual therapy technique: a randomized controlled trial.Functional chronic constipationPhysical Medicine / Rehabilitation - PhysiotherapyOral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colonACTRN12615000352505niversidad de Sevilla62
招募中
不适用
Pain and patient reported outcome measurements in carpal tunnel release and trigger finger release under local anesthesia with and without a tourniquet: a randomized controlled trialNL-OMON28454o sponsors140
尚未招募
4 期
Reduction in Pain after Topical Application of Lignocaine gel, Flavored lignocaine gel and Honey in Children Aged 6–12 years requiring Local anaesthesia Infiltration for Dental Treatment.CTRI/2024/02/063133Dr Krishna Kajave
招募中
不适用
A pilot study to the relation between altered pain perception and emotional blunting in schizophrenic patientspsychosis10039628schizophreniaNL-OMON30294Parnassia (Den Haag)75
招募中
Unknown
A retrospective clinical study of pain and sensory changes after breast cancer surgerybreast cancerJPRN-jRCT1050210104Shimazu Kenzo140
