Traditional Chinese Medicine Xiang-sha-liu-jun Granules in Patients With Postprandial Distress Syndrome(PDS)

• Status: Unknown status
• Trial end date: 2018-04-01
• Target enrollment: 0
• Participant gender: All

Summary

Functional dyspepsia (FD), which is one of the most common gastrointestinal disorders with high disease burden. Postprandial distress syndrome (PDS) is a common subtype of FD. Although the effectiveness of Chinese herbal formula of Xiang-sha-liu-jun granule (XSLJG) for alleviating PDS symptoms has been assessed in previous studies, more convinced evidence of randomized placebo-controlled study is needed.

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Xiyuan Hospital of China Academy of Chinese Medical Sciences
• Collaborators: The First Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine; Wuhan Integrated TCM and Western Medicine Hospita

Criteria

Inclusion Criteria:

• i)Aging between 18 and 75 years, able to read and write Chinese;

• ii)have a TCM diagnosis of spleen deficiency and qi stagnation pattern;

• iii) Having normal esophagogastroduodenoscopy results within 6 months;

• iv) Having normal liver and renal function confirmed by blood tests within 3 months;

• v) Being diagnosed as PDS of FD by a specialist consultation;

• vi）Receiving no other treatments during the study;

• vii）Voluntarily agreeing with the study protocol and signing a written informed consent.

Exclusion Criteria:

• i)Having peptic ulcer or gastroesophageal reflux disease confirmed by esophagogastroduodenoscopy;

• ii) Having obvious signs of irritable bowel syndrome;

• iii) Having alarm symptoms (weight loss, black or tar stool, or dysphagia);

• iv) Having serious structural disease (disease of heart, lung, liver or kidney) or mental illness;

• v) Having had surgery related with the gastrointestinal tract, except for appendectomy more than six months ago;

• vi) Pregnant or breastfeeding;

• vii) Being taking drugs which may affect the gastrointestinal tract; a minimum wash-out period of two weeks is required before participating in the trial;

• viii) Having a problem of malabsorption or maldigestion;

• ix) Having a history of allergies to the studied drugs and food;

• x) Having difficulties in attending the trial (such as paralysis, serious mental illness, dementia, renal diseases, stroke, coronary atherosclerotic heart diseases, diabetes or mental diseases, illiteracy);

• xi) Unwilling to sign the informed consent.