KCT0002229
Not yet recruiting
未知
The influence of patient-clinician interaction context on acupuncture outcomes in functional dyspepsia - a randomized controlled international multi-center trial
Kyung Hee University Oriental Medical Center0 sites59 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Kyung Hee University Oriental Medical Center
- Enrollment
- 59
- Status
- Not yet recruiting
- Last Updated
- 7 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •(1\) Age between 20 and 65 years
- •(2\) Meeting the definition of Functional Dyspepsia(FD) and Postprandial distress syndrome (PDS) as a subtype of Functional Dyspepsia according to the Rome III criteria
- •(3\) Complaints of a degree of dyspepsia more than 40 points on the visual analogue scale (VAS; 0, no symptom at all; 100, the most severe symptom one has ever had)
- •(4\) Individuals who agreed not to take any other new treatments associated with Functional Dyspepsia during the study
- •(5\) Individuals who voluntarily agreed and singed informed consent form
Exclusion Criteria
- •(1\) Have abnormal esophagogastroduodenoscopy results recently or evidence of any organic diseases affecting gastrointestinal tract (e.g. erosive esophagitis, peptic ulcer, dysplasia, mucosa\-associated, lymphoid tissue lymphoma, esophageal cancer, gastric cancer)
- •(2\) Individuals who have apparent signs of irritable bowel syndrome
- •(3\) Individuals who have alarmingsymptoms (weight loss, black or tarry stool, or dysphagia)
- •(4\) Individuals who have serious structural organ diseases (diseases of the heart, lung, liver, or kidney) or mental illness
- •(5\) Individuals who have undergone surgery related to the gastrointestinal tract (except for appendectomy performed for more than 6 months ago)
- •(6\) Individuals who are pregnant or breastfeeding
- •(7\) Individuals who are taking drugs that could affect the gastrointestinal tract ; a minimum wash\-out period of 2 weeks is required before participating in the trial.
- •(8\) Individuals who have participated other clinical trial within 1 month from the present
- •(9\) Individuals who are positive for human immunodeficiency virus infection
- •(10\) Individuals who are taking herbal medicine or oriental remedy that associated with dyspepsia / drugs that are considered inappropriate for this study
Outcomes
Primary Outcomes
Not specified
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