跳至主要内容
临床试验/NCT03501771
NCT03501771已完成不适用

Effects of Acupuncture on the Radial Pressure Pulse-wave at Cunkou in Low Back Pain

China Medical University Hospital2 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2018年4月25日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
42
试验地点
2
主要终点
Assessment of Radial Pressure Pulse-wave at cunkou (3)

研究概览

简要总结

Introduction: In TCM, Pulse Diagnosis has been one of the key diagnostic components in the clinical examinations. Traditionally, the palpation of the pulse on the radial artery is subjective among the physicians. With the development of the various devices to study the radial pressure pulse wave (RPPW), these have provided a scientific and objective assessment to assist the physicians on diagnosis and treatment. The primary objective of this intervention study is to investigate the effects of Acupuncture on the RPPW at cunkou in Low Back Pain (LBP) through the pulse sphygmograph. The secondary objective is to investigate the effect of acupoint combinations on different type LBP based on TCM syndrome differentiation through the primary and secondary outcome evaluations.

Methods: A single group, pre-post intervention study in which all participants receiving the same intervention will be conducted. A total 80 participants that meet all the following criteria will be enrolled: a. at least 20 years of age of either gender; b. chief complaint being low back pain; c. diagnosis with Lumbago (ICD-9-CM 724.2) or low back pain: loin pain, low back strain and lumbago NOS (not otherwise specified) (ICD-10-CM M54.4); d. diagnosis with lumbago with sciatica (ICD-10-CM M54.5). All participants will undergo acupuncture at BI23, BI25 & Bl40 after obtaining written informed consent. Objective and subjective baseline assessments and outcome evaluations including Vital Signs, health status questionnaire, Constitution in Chinese Medicines Questionnaire (CCMQ), Oswestry Disability Index, Faces Pain Scale-Revised (FPS-R) will be performed. The primary outcome will be the assessment of RPPW at cunkou ie at Cun, Guan & Chi of both hands using Pulse Sphygmograph before and after the intervention. The secondary outcome involves evaluating low back pain using the Fingertips-to-floor test & FPS-R before and after the intervention.

Expected Outcome: The results will be analyzed and provide information which can serve as clinical evidence of the influence of acupuncture on the RPPW at cunkou. In addition, the effectiveness of the acupoint combinations on the different type of LBP based on TCM syndrome differentiation can be further investigated.

详细描述

Introduction

In TCM, Pulse Diagnosis has been one of the key diagnostic components in the clinical examinations. Traditionally, the palpation of the pulse on the radial artery is subjective among the physicians. With the development of the various devices to study the radial pressure pulse wave (RPPW), these have provided a scientific and objective assessment to assist the physicians on diagnosis and treatment. The primary objective of this intervention study is to investigate the effects of Acupuncture on the RPPW at cunkou in Low Back Pain (LBP) through the pulse sphygmograph. The secondary objective is to investigate the effect of acupoint combinations on different type LBP based on TCM syndrome differentiation through the primary and secondary outcome evaluations.

Methods: A single group, pre-post intervention study in which all participants receiving the same intervention will be conducted. A total 80 participants that meet all the following criteria will be enrolled: a. at least 20 years of age of either gender; b. chief complaint being low back pain; c. diagnosis with Lumbago (ICD-9-CM 724.2) or low back pain: loin pain, low back strain and lumbago NOS (not otherwise specified) (ICD-10-CM M54.4); d. diagnosis with lumbago with sciatica (ICD-10-CM M54.5). All participants will undergo acupuncture at BI23, BI25 & Bl40 after obtaining written informed consent. Objective and subjective baseline assessments and outcome evaluations including Vital Signs, health status questionnaire, Constitution in Chinese Medicines Questionnaire (CCMQ), Oswestry Disability Index, Faces Pain Scale-Revised (FPS-R) will be performed. The primary outcome will be the assessment of RPPW at cunkou ie at Cun, Guan & Chi of both hands using Pulse Sphygmograph before and after the intervention. The secondary outcome involves evaluating low back pain using the Fingertips-to-floor test & FPS-R before and after the intervention.

Expected Outcome: The results will be analyzed and provide information which can serve as clinical evidence of the influence of acupuncture on the RPPW at cunkou. In addition, the effectiveness of the acupoint combinations on the different type of LBP based on TCM syndrome differentiation can be further investigated.

Other information: The study will be conducted in China Medical University Hospital (Meide Medical Building) Acupuncture Department at No. 166, Meide St, North District, Taichung, 404. It is anticipated that there will be not more than minimum risks encountered by the participants under careful needling by qualified TCM physician with minimum 10 years of clinical experiences. Data collection shall begin as soon as the IRB approval from CMUH Research Ethics Committee is obtained as well as the required equipment is available. Expected completion date: 1 yr from IRB approval.

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

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

入选标准

  • at least 20 years of age of either gender;
  • chief complaint being low back pain;
  • diagnosis with Lumbago (ICD-9-CM 724.2) or low back pain: loin pain, low back strain and lumbago NOS (not otherwise specified) (ICD-10-CM M54.4);
  • diagnosis with lumbago with sciatica (ICD-10-CM M54.5).

排除标准

  • Pregnancy or lactation
  • CHF, carcinomas under chemotherapy, psychological/psychiatric disorders
  • Heart diseases with transplanted device such as pacemaker.
  • Acute infections eg Upper Respiratory Infection (URI), Urinary Tract Infections (UTI), Acute gastroenteritis.
  • Inability to undergo evaluation with the Pulse Sphygmograph
  • Alcohol abuse or drug addiction
  • Communication disorder
  • Refusal to provide informed consent or participate in the study
  • Exclusion at Project Investigator's discretion
  • Participation in other clinical trials within 3 months
  • Allergic to metal

研究组 & 干预措施

Acupuncture

Experimental

Acupuncture needle will be administered.

干预措施: Acupuncture (Other)

结局指标

主要结局

Assessment of Radial Pressure Pulse-wave at cunkou (3)

时间窗: 10 min after acupuncture

Assessment of Radial Pressure Pulse-wave at cunkou ie at Cun, Guan \& Chi of both hands before and after the intervention using Pulse Sphygmograph at 10 min after acupuncture.

Assessment of Radial Pressure Pulse-wave at cunkou (1)

时间窗: 30 min before acupuncture

Assessment of Radial Pressure Pulse-wave at cunkou ie at Cun, Guan \& Chi of both hands before and after the intervention using Pulse Sphygmograph at 30 min before acupuncture.

Assessment of Radial Pressure Pulse-wave at cunkou (2)

时间窗: 10 min before acupuncture

Assessment of Radial Pressure Pulse-wave at cunkou ie at Cun, Guan \& Chi of both hands before and after the intervention using Pulse Sphygmograph at 10 min before acupuncture.

次要结局

  • Range of Motion: Fingertip-to-Floor (FTF) test(1) 10 min before acupuncture; 2) 10 min after needle removal)
  • Faces Pain Scale - Revised (FPS-R)(1) 20 min before acupuncture; 2) 10 min after needle removal)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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