跳至主要内容
临床试验/NCT01002846
NCT01002846Unknown3 期

Effects of Acupuncture at ST36 and PC6 on Blood Pressure and Endothelial

Kyunghee University Medical Center1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2009年9月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
入组人数
32
试验地点
1
主要终点
To assess effects of acupuncture on endothelial function with FMD variation after 8 weeks treatments.

研究概览

简要总结

This is randomised, controlled study about effects of acupuncture on blood pressure and endothelial dysfunction in stage I hypertension patient without medication. Subject will receive 8 weeks of either acupuncture or sham acupuncture, measuring FMD and blood test before and after 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
Single (Participant)

入排标准

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

入选标准

  • •Patients age 18-70 diagnosed stage I hypertension ( JNC-7) without taking hypertensive medication

排除标准

  • •Secondary hypertension
  • •History of cardiovascular disease
  • •Taking hypertensive medication
  • •Taking hyperlipidemic medication
  • •Pregnancy or feeding woman
  • •Cannot follow indication or there is no agreement of patient and conservator
  • •Investigator decide Inappropriate to trial

研究组 & 干预措施

traditional acupuncture

Experimental

Procedure : ST 36 and PC 6 are selected, subject will undergo 20minute sessions twice a week for 8weeks. Disposable acupuncture needle(4cm sterilized stainless steel) will be inserted up to 1 cm depth

干预措施: acupuncture (Procedure)

sham acupuncture

Sham Comparator

Procedure : Beside 1cm of ST 36 and PC 6 are selected( not meridian point), subject will undergo 20 minute. Disposable acupuncture needle(4cm sterilized stainless steel) will be inserted under 1 cm slightly.

干预措施: acupuncture (Procedure)

结局指标

主要结局

To assess effects of acupuncture on endothelial function with FMD variation after 8 weeks treatments.

时间窗: 8 weeks

次要结局

  • To examine the effects of acupuncture on blood pressure, lipid , hsCRP level variation with ABPM after 8 weeks treatments.(8 weeks)

研究者

申办方类型
Other

研究点 (1)

Loading locations...

相似试验