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Not yet recruitingNCT07715760Updated Jul 20, 2026

Efficacy and Mechanistic Evaluation of Hewei Anchang Formula for Overlapping Gastrointestinal Symptoms in Patients With Coexisting Functional Dyspepsia and Diarrhea-Predominant Irritable Bowel Syndrome

An interventional study of Hewei Anchang Formula Granules and Hewei Anchang Formula Matching Placebo Granules in Functional Dyspepsia and Irritable Bowel Syndrome With Diarrhea, sponsored by Xiyuan Hospital of China Academy of Chinese Medical Sciences. Not yet recruiting at 1 site in China. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-07-20.

Sponsored by Xiyuan Hospital of China Academy of Chinese Medical Sciences · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

  1. To conduct a multicenter, randomized controlled trial across four hospitals to evaluate the efficacy of Hewei Anchang Formula in patients with overlapping gastrointestinal symptoms of functional dyspepsia (FD) and diarrhea-predominant irritable bowel syndrome (IBS-D), characterized by liver-stomach disharmony syndrome and liver stagnation-spleen deficiency syndrome, respectively. By leveraging the holistic regulatory effects of Chinese herbal formulas and the traditional Chinese medicine principle of "treating different diseases with the same therapeutic approach," this study aims to generate high-level evidence for the management of overlapping gastrointestinal symptoms in functional gastrointestinal disorders (FGIDs) and to establish a standardized and scalable therapeutic strategy.
  2. To elucidate the potential mechanisms underlying the therapeutic effects of Hewei Anchang Formula on overlapping gastrointestinal symptoms of FD and IBS-D through multiple targets and pathways, with particular emphasis on modulation of the gut microbiota and the neuroendocrine-immune network.
Read the detailed description

Functional gastrointestinal disorders (FGIDs) comprise a group of gastrointestinal conditions characterized predominantly by gastrointestinal symptom complexes in the absence of identifiable structural abnormalities or clearly defined pathophysiological mechanisms. Individual FGIDs are diagnosed primarily on the basis of symptom profiles and commonly present with manifestations such as reflux, heartburn, dyspepsia, abdominal pain, bloating, diarrhea, and constipation. The boundaries between different FGIDs are not distinct, and symptom overlap is common. Such overlap not only increases disease complexity and substantially complicates clinical diagnosis and management, but also increases healthcare utilization and imposes a considerable adverse impact on patients' quality of life. According to the Rome IV criteria, each patient with an FGID receives, on average, 1.5 FGID diagnoses, and approximately 36% of patients have FGIDs involving two or more gastrointestinal regions, representing a typical pattern of symptom overlap.

Among the various overlapping phenotypes of FGIDs, the coexistence of functional dyspepsia (FD) and diarrhea-predominant irritable bowel syndrome (IBS-D) is one of the most common. These patients experience both typical upper gastrointestinal symptoms of FD, including postprandial fullness, early satiety, and epigastric pain, and core lower gastrointestinal manifestations of IBS-D, such as abdominal pain, diarrhea, and altered stool form, making this overlap phenotype a major challenge in gastroenterological practice. Compared with patients with FD or IBS-D alone, those with coexisting FD and IBS-D tend to experience more persistent, frequent, and severe symptoms. These symptoms can substantially affect eating habits, daily routines, social activities, and other aspects of everyday life, thereby markedly impairing quality of life. Repeated healthcare-seeking behavior also increases both individual medical expenditures and the consumption of healthcare resources, making this condition an important clinical and public health concern requiring effective intervention.

The clinical management of overlapping gastrointestinal symptoms in FGIDs remains challenging. Conventional pharmacological treatments often act on limited therapeutic targets and may therefore provide suboptimal efficacy in patients with overlapping symptom profiles, while also contributing to a substantial socioeconomic burden. Commonly used medications, including prokinetic agents, proton pump inhibitors, antidiarrheal agents, and anticholinergic antispasmodics, generally target symptoms arising from a single gastrointestinal region. Consequently, treatment outcomes may be unsatisfactory when upper and lower gastrointestinal symptoms coexist. Although combination pharmacotherapy may address multiple symptoms, it may also increase the risk of adverse drug reactions, and some patients discontinue treatment because of poor tolerability or adverse effects, resulting in limited overall clinical benefit. In addition, the pathophysiology of coexisting FD and IBS-D is complex and has been associated with multiple interacting mechanisms, including gastrointestinal dysmotility, gut microbial dysbiosis, and dysregulation of the neuroendocrine-immune network. Thus, single-target pharmacotherapy may be poorly suited to the multifactorial pathophysiological features of this overlap phenotype, which may partly explain its limited therapeutic effectiveness.

Patients with FD and IBS-D frequently experience psychological disturbances, including anxiety and depression. From the perspective of traditional Chinese medicine (TCM), liver qi stagnation is considered a key underlying pathogenesis, while spleen-stomach deficiency and liver stagnation with spleen deficiency are among the most common syndrome patterns in patients with overlapping FD and IBS-D. Accordingly, strengthening the spleen and regulating qi, as well as soothing the liver and strengthening the spleen, are regarded as core therapeutic principles. Owing to its holistic regulatory effects and individualized treatment based on syndrome differentiation, TCM may be particularly well suited to the multifactorial pathophysiology of overlapping FGIDs. Guided by the TCM principle of "treating different diseases with the same therapeutic approach," TCM interventions may target the shared pathogenesis of liver stagnation with spleen deficiency through multicomponent, multitarget, and multipathway mechanisms, thereby exerting integrated effects on gastrointestinal function, emotional well-being, and internal homeostasis. This therapeutic model may offer advantages over conventional single-target symptomatic treatment.

Chaihu Shugan San has the traditional actions of regulating qi, relieving stagnation, harmonizing the stomach, and redirecting rebellious qi downward, and has been strongly recommended in several expert consensuses and clinical guidelines for the treatment of FD with liver-stomach disharmony syndrome. Based on more than four decades of clinical experience, Professor Xudong Tang of Xiyuan Hospital, China Academy of Chinese Medical Sciences, proposed the theory of "regulating the middle and restoring balance." Under the guidance of this theory, Chang'an I Formula was developed according to the core pathogenesis of IBS-D. Hewei Anchang Formula is an optimized herbal formula derived from Chang'an I Formula and modified Chaihu Shugan San, with modifications tailored to the pathophysiological characteristics of liver-stomach disharmony syndrome in FD and liver stagnation with spleen deficiency syndrome in IBS-D. The formula has demonstrated promising clinical effects. Based on the theory of "regulating the middle and restoring balance," Hewei Anchang Formula is designed to address the core pathogenesis of overlapping gastrointestinal symptoms in FD and IBS-D, with therapeutic actions aimed at strengthening the spleen, soothing the liver, regulating qi, and alleviating diarrhea. Its composition is therefore closely aligned with the principles of TCM syndrome differentiation and provides a suitable intervention for investigating TCM-based treatment of this overlap phenotype.

This study is designed as a multicenter, randomized, double-blind, placebo-controlled clinical trial and will enroll 120 patients with overlapping gastrointestinal symptoms of FD with liver-stomach disharmony syndrome and IBS-D with liver stagnation-spleen deficiency syndrome. The study aims to evaluate the clinical efficacy and potential therapeutic advantages of Hewei Anchang Formula in the treatment of coexisting FD and IBS-D. Metagenomic and metabolomic approaches will also be used to investigate its potential mechanisms of action, with particular emphasis on the gut microbial ecosystem and the neuroendocrine-immune network. The findings are expected to provide a practical TCM-based therapeutic strategy for improving the overall management of overlapping gastrointestinal symptoms in FGIDs and reducing the associated medical and socioeconomic burden.

02

Conditions studied

  • Functional Dyspepsia
  • Irritable Bowel Syndrome With Diarrhea

Keywords

  • Hewei Anchang Formula
  • Overlapping Gastrointestinal Symptoms
  • Functional Gastrointestinal Disorders
  • Traditional Chinese Medicine
  • Chinese Herbal Medicine
  • Gut Microbiota
  • Metagenomics
  • Metabolomics
03

In context

Gastrointestinal Diseases

548 studies on the registry are indexed under Gastrointestinal Diseases; 101 are open to participants now.

This study's planned enrollment of 120 is above the median of 80 across 388 interventional studies indexed under Gastrointestinal Diseases.

Browse Gastrointestinal Diseases studies →

Lead sponsor

Xiyuan Hospital of China Academy of Chinese Medical Sciences is the lead sponsor of 43 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Meet the Rome IV diagnostic criteria for both functional dyspepsia (FD) and diarrhea-predominant irritable bowel syndrome (IBS-D).
  2. Meet the diagnostic criteria for liver-stomach disharmony syndrome in FD and liver qi stagnation with spleen deficiency syndrome in IBS-D.
  3. Aged 18-65 years, with no restriction on sex.
  4. Fully informed about the study and voluntarily provide written . -

Exclusion criteria

Exclusion Criteria:

  1. Severe primary diseases of the cardiovascular, hepatic, renal, hematologic, or respiratory systems, or malignant tumors.
  2. Other organic gastrointestinal diseases, such as peptic ulcer or ulcerative colitis, or systemic diseases that may affect gastrointestinal motility, such as hyperthyroidism or diabetes mellitus.
  3. Current or anticipated continuous use of medications that may affect gastrointestinal function, including prokinetic agents, antidiarrheal agents, antidepressants, anxiolytics, gut microbiota-modulating agents, and antibiotics.
  4. A history of allergy to any study-related medication or a history of severe food allergy.
  5. Psychiatric disorders, intellectual impairment, or language impairment.
  6. Women who are planning pregnancy, pregnant, or breastfeeding.
  7. Current participation in another drug clinical trial or participation in another drug clinical trial within the previous 4 weeks.
  8. Severe anxiety or depression, as assessed using the Hospital Anxiety and Depression Scale (HADS). An anxiety subscale score of ≥15 is defined as severe anxiety, and a depression subscale score of ≥15 is defined as severe depression. Participants meeting the criterion for severe anxiety or severe depression on either subscale will be excluded.
  9. A suspected or confirmed history of alcohol or drug abuse, or other circumstances that, in the investigator's judgment, may reduce the likelihood of enrollment or complicate study participation, such as frequent changes in the work environment that may increase the risk of loss to follow-up. -
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

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05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    Hewei Anchang Formula Group

    Participants assigned to this group will receive Hewei Anchang Formula granules orally, one sachet twice daily for 4 weeks. Each dose will be dissolved in approximately 100 mL of warm water and taken 1 hour after breakfast and dinner.

    Drug: Hewei Anchang Formula Granules

  • Placebo comparator
    Placebo Group

    Participants assigned to this group will receive matching placebo granules containing 5% Hewei Anchang Formula granules, one sachet twice daily for 4 weeks. Each dose will be dissolved in approximately 100 mL of warm water and taken 1 hour after breakfast and dinner.

    Drug: Hewei Anchang Formula Matching Placebo Granules

Interventions

  • DrugHewei Anchang Formula Granules

    Hewei Anchang Formula granules will be administered orally at a dose of one sachet twice daily for 4 weeks. Each dose will be dissolved in approximately 100 mL of warm water and taken 1 hour after breakfast and dinner.

  • DrugHewei Anchang Formula Matching Placebo Granules

    The matching placebo granules contain 5% Hewei Anchang Formula granules and will be administered orally at a dose of one sachet twice daily for 4 weeks. Each dose will be dissolved in approximately 100 mL of warm water and taken 1 hour after breakfast and dinner.

06

What researchers measure

Primary outcomes

  1. Functional Dyspepsia Symptom Severity Scale Scores

    The scale assesses the frequency and severity of four functional dyspepsia symptoms: postprandial fullness, early satiation, epigastric pain, and epigastric burning. For each symptom, frequency is rated on a 5-point scale ranging from 1 (never) to 5 (present throughout the day), and severity is rated on a 4-point scale ranging from 1 (none) to 4 (severe).

    Time frame: Baseline (Day 0), Week 2, Week 4, and Week 8

  2. Global Impression Scale for Dyspepsia Symptom Relief

    Participants will evaluate the overall relief of dyspepsia-related symptoms during the previous 2 weeks using a 7-point scale: 1 = markedly worse, 2 = worse, 3 = slightly worse, 4 = no relief, 5 = slight relief, 6 = marked relief, and 7 = complete relief. Higher scores indicate greater overall symptom relief.

    Time frame: Baseline (Day 0), Week 2, Week 4, and Week 8

  3. Irritable Bowel Syndrome Severity Scoring System (IBS-SSS) Score

    The IBS-SSS assesses abdominal pain severity, the number of days with abdominal pain during a 14-day period, abdominal distension severity, satisfaction with bowel habits, and the extent to which irritable bowel syndrome interferes with daily life. Higher scores indicate greater symptom severity.

    Time frame: Baseline (Day 0), Week 2, Week 4, and Week 8

Secondary outcomes

  1. Traditional Chinese Medicine Syndrome Score

    The Traditional Chinese Medicine syndrome score assesses 15 symptoms: epigastric fullness, epigastric pain, reduced appetite, heartburn or a burning sensation, belching or acid regurgitation, excessive clear salivation, a sensation of obstruction in the throat, thirst without a desire to drink, lower abdominal distension or pain, limb weakness, shortness of breath, disinclination to speak, heaviness of the body and limbs, aversion to cold, and loose stools. Each item is rated from 0 (none) to 3 (severe). The item scores are summed to obtain a total score ranging from 0 to 45, with higher scores indicating greater symptom severity.

    Time frame: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days

  2. Irritable Bowel Syndrome Quality of Life Questionnaire (IBS-QOL) Score

    The IBS-QOL questionnaire used in this study contains 13 items assessing the impact of bowel problems on feelings of helplessness, embarrassment, time spent in the bathroom, health concerns, body image, daily planning, happiness, comfort when discussing bowel problems, frustration, social relationships, food intake, sexual life, and anger. Each item is rated from 0 (not at all) to 4 (completely true), with higher raw scores indicating a greater negative impact of bowel problems on quality of life.

    Time frame: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days

  3. Patient-Reported Outcome (PRO) Scale Total Score

    The 38-item Patient-Reported Outcome scale assesses upper and lower gastrointestinal symptoms, appetite- and eating-related symptoms, body weight, fatigue, sleep, emotional status, social activities, work-related functioning, and fear of gastroscopy. Each item is scored from 0 to 4. The item scores are summed to obtain a total score ranging from 0 to 152, with higher scores indicating a greater symptom burden and greater functional impact.

    Time frame: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days

  4. 36-Item Short Form Health Survey (SF-36) Scores

    The SF-36 assesses self-reported general health, changes in health status, physical functioning, limitations in work and daily activities due to physical or emotional health, social functioning, bodily pain, vitality, emotional well-being, and general health perceptions. Scores will be calculated using the item-specific response weights specified in the questionnaire.

    Time frame: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days

  5. Hospital Anxiety and Depression Scale (HADS) Score

    The Hospital Anxiety and Depression Scale consists of 14 items, including seven items assessing anxiety and seven items assessing depression. Each item is scored from 0 to 3. The anxiety and depression subscale scores each range from 0 to 21. Scores of 0-7 indicate no symptoms, scores of 8-10 indicate possible symptoms, and scores of 11-21 indicate definite symptoms.

    Time frame: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days

Other outcomes

  1. Fecal Gut Microbiome Metagenomic Profiles

    Fecal samples will undergo metagenomic analysis to characterize gut microbial profiles and their changes across the specified sampling time points.

    Time frame: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, and Week 4 ± 3 days

  2. Blood and Urine Metabolomic Profiles

    Blood and urine samples will undergo metabolomic analysis to characterize metabolic profiles and their changes across the specified sampling time points.

    Time frame: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, and Week 4 ± 3 days

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07715760
Lead sponsor
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Collaborators
Shanghai University of Traditional Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Responsible party
Sponsor
First posted
Jul 20, 2026
Start date
Jan 1, 2027 (estimated)
Primary completion
Jun 30, 2028 (estimated)
Completion
Dec 30, 2028 (estimated)
Last update
Jul 20, 2026

Study contacts

Lin Lv
Contact
lushangshitou@qq.com
86-18811782728

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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