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临床试验/ISRCTN12511434
ISRCTN12511434已完成未知

Efficacy of Acupuncture for Postprandial Distress Syndrome (PDS): a multi-centre, Randomized, Controlled Trial

Beijing Municipal Science & Technology Commission0 个研究点目标入组 278 人开始时间: 2017年3月31日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
278

研究概览

简要总结

2019 protocol in https://www.ncbi.nlm.nih.gov/pubmed/30658669 (added 21/01/2019) 2020 results in https://www.ncbi.nlm.nih.gov/pubmed/32422066 (added 19/05/2020)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • Current inclusion criteria as of 06/02/2018:
  • 1. 18-65 years old
  • 2. If they have epigastric pain syndrome symptoms (epigastric pain or epigastric burning), then the symptoms that are causing distress have to be one of the following meal-related symptoms: postprandial fullness, upper abdominal bloating or early satiation
  • 3. Normal esophagogastroduodenoscopy results within a year
  • 4. No acupuncture treatment in previous 1 month
  • 5. Never joined any other study in process in previous 2 months
  • Previous inclusion criteria:
  • 1. 18-65 years old
  • 2. If they have epigastric pain syndrome symptoms (epigastric pain or epigastric burning), then the symptoms that are causing distress have to be one of the following meal-related symptoms: postprandial fullness, upper abdominal bloating or early satiation
  • 3. Normal esophagogastroduodenoscopy results within a year
  • 4. No acupuncture treatment in previous 1 month
  • 5. No use of medicine for PDS during two weeks before enrollment
  • 6. Never joined any other study in process in previous 2 months

排除标准

  • Current exclusion criteria as of 06/02/2018:
  • 1. Functional dyspepsia (FD) symptoms caused by any serious or malignant disease
  • 2. Surgery related with the gastrointestinal tract
  • 3. Taking drugs which might affect dyspepsia, such as anti-secretary drugs, antacids, prokinetics, non-steroidal anti-inflammatory drugs and antidepressant drugs before 1 month participating in the trial
  • 4. Drug or alcohol abuse
  • 5. Pregnant women or women in lactation period
  • Previous exclusion criteria as of 11/01/2018:
  • 1. Functional dyspepsia (FD) symptoms caused by any serious or malignant disease
  • 2. Surgery related with the gastrointestinal tract
  • 3. Drug or alcohol abuse
  • 4. Pregnant women or women in lactation period
  • Previous exclusion criteria:
  • 1. Functional dyspepsia (FD) symptoms caused by any serious or malignant disease
  • 2. Surgery related with the gastrointestinal tract
  • 3. Taking drugs which might affect dyspepsia, such as anti-secretary drugs, antacids, prokinetics, non-steroidal anti-inflammatory drugs and antidepressant drugs before 1 month participating in the trial
  • 4. Drug or alcohol abuse
  • 5. Pregnant women or women in lactation period

研究者

发起方
Beijing Municipal Science & Technology Commission

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