Functional DyspepsiaNCT07715760
Efficacy and Mechanistic Evaluation of Hewei Anchang Formula for Overlapping Gastrointestinal Symptoms in Patients With Coexisting Functional Dyspepsia and Diarrhea-Predominant Irritable Bowel Syndrome
A study testing Hewei Anchang Formula Granules in people with Functional Dyspepsia and Irritable Bowel Syndrome With Diarrhea, run by Xiyuan Hospital of China Academy of Chinese Medical Sciences at 1 site in China.
Trial 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… Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Functional Dyspepsia, Irritable Bowel Syndrome With Diarrhea
- What is being tested?
- Hewei Anchang Formula Granules
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 120 participants
- Where
- 1 siteChina
- Study dates
- 1 Jan 2027to 30 Dec 2028
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Meet the Rome IV diagnostic criteria for both functional dyspepsia (FD) and diarrhea-predominant irritable bowel syndrome (IBS-D).
- Meet the diagnostic criteria for liver-stomach disharmony syndrome in FD and liver qi stagnation with spleen deficiency syndrome in IBS-D.
- Aged 18-65 years, with no restriction on sex.
- Fully informed about the study and voluntarily provide written informed consent. -
Who cannot join
- Severe primary diseases of the cardiovascular, hepatic, renal, hematologic, or respiratory systems, or malignant tumors.
- 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.
- 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.
- A history of allergy to any study-related medication or a history of severe food allergy.
- Psychiatric disorders, intellectual impairment, or language impairment.
- Women who are planning pregnancy, pregnant, or breastfeeding.
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- Current participation in another drug clinical trial or participation in another drug clinical trial within the previous 4 weeks.
- 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.
- 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. -
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
China1 site
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Beijing, Beijing Municipality, 100091
About this study
- 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.
- 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.
- Being tested
- Hewei Anchang Formula Granules, Hewei Anchang Formula Matching Placebo Granules
- Keywords
- Hewei Anchang Formula, Overlapping Gastrointestinal Symptoms, Functional Gastrointestinal Disorders, Traditional Chinese Medicine, Chinese Herbal Medicine, Gut Microbiota, Metagenomics, Metabolomics
- Medical subject headings
- Gastrointestinal Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Hewei Anchang Formula GranulesDrug
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.
Hewei Anchang Formula Matching Placebo GranulesDrug
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.
| Study group | Role | What they receive |
|---|---|---|
| Hewei Anchang Formula Group | Experimental | 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. Receives: Drug: Hewei Anchang Formula Granules |
| Placebo Group | Placebo comparator | 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. Receives: Drug: Hewei Anchang Formula Matching Placebo Granules |
What is being measured
The primary outcome is the main question the study is designed to answer.
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).
Measured: Baseline (Day 0), Week 2, Week 4, and Week 8
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.
Measured: Baseline (Day 0), Week 2, Week 4, and Week 8
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.
Measured: Baseline (Day 0), Week 2, Week 4, and Week 8
Secondary outcomes (5)
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.
Measured: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days
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.
Measured: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days
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.
Measured: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days
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.
Measured: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days
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.
Measured: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Jul 2026
- Study start1 Jan 2027 (estimated)
- Primary completion30 Jun 2028 (estimated)
- Study completion30 Dec 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Functional DyspepsiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 120 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Xiyuan Hospital of China Academy of Chinese Medical Sciences
- Sponsor type
- University, hospital or other
- 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
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07715760
- Sponsor's protocol ID
- CI2026A01002
- Status last verified
- Jul 2026
- First submitted
- 11 Jul 2026
- Last updated
- 20 Jul 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 20 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Efficacy and Mechanistic Evaluation of Hewei Anchang Formula for Overlapping Gastrointestinal Symptoms in Patients With Coexisting Functional Dyspepsia and Diarrhea-Predominant Irritable Bowel Syndrome
- ClinicalTrials.gov ID
- NCT07715760
- Acronym / sponsor ID
- CI2026A01002
- Keywords
- Hewei Anchang Formula, Overlapping Gastrointestinal Symptoms, Functional Gastrointestinal Disorders, Traditional Chinese Medicine, Chinese Herbal Medicine, Gut Microbiota, Metagenomics, Metabolomics
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 120 participants (estimated)
- Lead sponsor
- Xiyuan Hospital of China Academy of Chinese Medical SciencesUniversity, hospital or other
- 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
- Study start
- 1 Jan 2027 (estimated)
- Primary completion
- 30 Jun 2028 (estimated)
- Study completion
- 30 Dec 2028 (estimated)
- First posted
- 20 Jul 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
- 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.
- 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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Hewei Anchang Formula Group | Experimental | Drug: Hewei Anchang Formula GranulesParticipants 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. |
| Placebo Group | Placebo comparator | Drug: Hewei Anchang Formula Matching Placebo GranulesParticipants 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. |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Meet the Rome IV diagnostic criteria for both functional dyspepsia (FD) and diarrhea-predominant irritable bowel syndrome (IBS-D).
- Meet the diagnostic criteria for liver-stomach disharmony syndrome in FD and liver qi stagnation with spleen deficiency syndrome in IBS-D.
- Aged 18-65 years, with no restriction on sex.
- Fully informed about the study and voluntarily provide written informed consent. -
Key exclusion criteria (9 listed)
- Severe primary diseases of the cardiovascular, hepatic, renal, hematologic, or respiratory systems, or malignant tumors.
- 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.
- 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.
- A history of allergy to any study-related medication or a history of severe food allergy.
- Psychiatric disorders, intellectual impairment, or language impairment.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Hewei Anchang Formula GranulesHewei 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. | Drug | Hewei Anchang Formula Group |
| Hewei Anchang Formula Matching Placebo GranulesThe 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. | Drug | Placebo Group |
Primary outcome
Functional Dyspepsia Symptom Severity Scale Scores
Time frame: Baseline (Day 0), Week 2, Week 4, and Week 8
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).
Global Impression Scale for Dyspepsia Symptom Relief
Time frame: Baseline (Day 0), Week 2, Week 4, and Week 8
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.
Irritable Bowel Syndrome Severity Scoring System (IBS-SSS) Score
Time frame: Baseline (Day 0), Week 2, Week 4, and Week 8
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.
5 secondary outcomes
Traditional Chinese Medicine Syndrome Score
Time frame: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days
Irritable Bowel Syndrome Quality of Life Questionnaire (IBS-QOL) Score
Time frame: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days
Patient-Reported Outcome (PRO) Scale Total Score
Time frame: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days
36-Item Short Form Health Survey (SF-36) Scores
Time frame: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days
Hospital Anxiety and Depression Scale (HADS) Score
Time frame: Baseline (Day 0 ± 3 days), Week 2 ± 3 days, Week 4 ± 3 days, and Week 8 ± 3 days
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Jul 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Hewei Anchang Formula Granules in people with Functional Dyspepsia and Irritable Bowel Syndrome With Diarrhea, run by Xiyuan Hospital of China Academy of Chinese Medical Sciences at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 20 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Lin Lv (86-18811782728, lushangshitou@qq.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Functional Dyspepsia Symptom Severity Scale Scores (time frame: Baseline (Day 0), Week 2, Week 4, and Week 8). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Jul 2026.