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Phase III Clinical Trial of Changji'an Capsules in the Treatment of Irritable Bowel Syndrome With Predominant Diarrhea (Liver-Qi Invading Spleen Syndrome)

22 maggio 2026 aggiornato da: Shengsheng Zhang, Beijing Hospital of Traditional Chinese Medicine

Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase III Clinical Trial on the Efficacy and Safety of Changji'an Capsules in the Treatment of Irritable Bowel Syndrome With Predominant Diarrhea (Liver-Qi Invading Spleen Syndrome)

This trial is a randomized, double-blind, placebo-controlled, parallel-group, multicenter Phase III clinical trial. Its purpose is to evaluate the efficacy and safety of Changji'an Capsules in subjects with diarrhea-predominant irritable bowel syndrome (liver-qi invading spleen syndrome) after 8 weeks of treatment.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

636

Fase

  • Fase 3

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

  • Cina
      • Chengdu, Cina
        • West China Hospital, Sichuan University
      • Chongqing, Cina
        • Chongqing Traditional Chinese Medicine Hospital
      • Guangzhou, Cina
        • The First Affiliated Hospital of Guangzhou University of Chinese Medicine
      • Guizhou, Cina
        • The First Affiliated Hospital of Guizhou University of Traditional Chinese Medicine
      • Haozhou, Cina
        • Haozhou People's Hospital
      • Hebei, Cina
        • Hebei Provincial Hospital of Traditional Chinese Medicine
      • Heilongjiang, Cina
        • The First Affiliated Hospital of Heilongjiang University of Chinese Medicine
      • Hubei, Cina
        • Hubei Provincial Hospital of Traditional Chinese Medicine
      • Jinan, Cina
        • The Affiliated Hospital of Shandong University of Traditional Chinese Medicine
      • Kaifeng, Cina
        • Kaifeng Hospital of Traditional Chinese Medicine
      • Luoyang, Cina
        • Luoyang First People's Hospital
      • Nanjing, Cina
        • Jiangsu Provincial Hospital of Traditional Chinese Medicine
      • Shanghai, Cina
        • Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
      • Shanxi, Cina
        • The Affiliated Hospital of Shaanxi University of Chinese Medicine
      • Shaoyang, Cina
        • Shaoyang Central Hospital
      • Shiyan, Cina
        • Shiyan People's Hospital
      • Tianjin, Cina
        • The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine
      • Tianjin, Cina
        • The Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine
      • Wenzhou, Cina
        • Wenzhou Traditional Chinese Medicine Hospital
      • Wuhan, Cina
        • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
      • Wuxi, Cina
        • Wuxi Traditional Chinese Medicine Hospital
      • Xi'an, Cina
        • The Second Affiliated Hospital of Xi'an Jiaotong University
      • Xi'an, Cina
        • Xi'an Central Hospital
      • Xingtai, Cina
        • Xingtai People's Hospital
      • Yueyang, Cina
        • Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine
      • Zhejiang, Cina
        • Zhejiang Provincial Hospital of Traditional Chinese Medicine
      • Zhengzhou, Cina
        • Zhengzhou First People's Hospital
      • Zhujiang, Cina
        • Zhujiang Hospital, Southern Medical University
    • Dongcheng District
      • Beijing, Dongcheng District, Cina, 100010
        • Beijing Hospital of Traditional Chinese Medicine
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  1. Meet the Western medicine diagnostic criteria for diarrhea-predominant irritable bowel syndrome;
  2. Meet the Traditional Chinese Medicine syndrome differentiation criteria for liver Qi invading the spleen;
  3. Aged ≥18 and ≤65 years, regardless of gender;
  4. Record daily the most severe abdominal pain, bloating, and abdominal discomfort NRS scores for the last week of the run-in period. At least one of these three items must meet the weekly average NRS score criterion (the weekly average of abdominal pain NRS is calculated as: total weekly score of abdominal pain NRS on days with Bristol Stool Form Scale type 6 or 7 stools / actual number of days with Bristol type 6 or 7 stools in that week; the average values for the other two items are calculated similarly) ≥3 points (11-point Numerical Rating Scale, NRS-11); meanwhile, for stool form, during the last week of the run-in period, there must be at least 2 days in which each day has at least one bowel movement of Bristol type 6 or 7;
  5. Self-Rating Anxiety Scale (SAS) <60 points and Self-Rating Depression Scale (SDS) <63 points;
  6. Have a colonoscopy result showing no obvious abnormalities (including diverticula or chronic inflammation) or colon polyps, based on colonoscopy results within 12 months prior at a tertiary hospital: 1.Colonoscopy results are normal with no organic changes; 2. Colonoscopy report shows minor abnormalities such as hemorrhoids or colonic polyps (diameter ≤5mm and number ≤3), which the investigator deems eligible for inclusion; 3. Previous colonoscopy reported colonic polyps with diameter >5mm or number >3, but after endoscopic treatment within 6 months prior to screening, remaining polyps are ≤5mm in diameter and ≤3 in number, deemed eligible by the investigator;
  7. Agree to participate in this clinical trial and voluntarily sign the informed consent form.

Exclusion Criteria:

  1. Individuals with fewer than 3 spontaneous bowel movements per week during the induction period;
  2. Individuals with stool consistency of type 1 or 2 (Bristol Stool Form Scale) on at least 2 days per week during the induction period;
  3. Individuals confirmed to have infectious diarrhea, inflammatory bowel disease, parasitic infection, positive fecal occult blood tests and considered to have gastrointestinal bleeding (excluding hemorrhoids), colorectal tumors, malabsorption syndrome, lactose intolerance (based on medical history), and diarrhea caused by systemic diseases;
  4. Individuals who have used other medications for irritable bowel syndrome within 1 week prior to screening;
  5. Individuals with non-IBS-D or other organic gastrointestinal lesions (excluding superficial gastritis, grade I erosive gastritis, or chronic atrophic gastritis found on endoscopy but deemed by the investigator to be eligible for inclusion (e.g., no mucosal erosion or bleeding observed endoscopically, and the patient has no upper abdominal fullness, upper abdominal pain, or acid reflux)), or other organic lesions that the investigator judges may cause abdominal pain, bloating, or discomfort;
  6. Individuals with diabetes, hyperthyroidism, or serious primary diseases of the cardiovascular, cerebrovascular, liver, kidney, hematopoietic systems, or other serious diseases affecting survival (e.g., tumors), abnormal liver and kidney function (AST, ALT > 1.5 times the upper limit of normal reference range, Scr above the upper limit of normal reference range), and clinically significant ECG abnormalities;
  7. Individuals with other mental disorders (excluding mild anxiety or depression);
  8. Individuals with a history of gastrointestinal surgery (excluding appendectomy or intestinal polyp removal);
  9. Individuals who, within 2 weeks prior to screening, are using or need to continue using medications that may affect gastrointestinal function (anticholinergic drugs, 5-HT3 receptor antagonists, antidiarrheal drugs, antacids, prokinetic drugs, antidepressants (fluoxetine for at least 28 days), anti-anxiety drugs, intestinal microbiota regulators, traditional Chinese medicine decoctions, etc.);
  10. Individuals allergic to 3 or more medications or foods, or known allergies to Xiangjie Capsules and its components, as well as emergency medication Pivabromium tablets;
  11. Individuals who took emergency medication (Pivabromium tablets) during the last week of the induction period;
  12. Individuals who took prohibited medications during the induction period;
  13. Individuals suspected of or confirmed with a history of alcohol or drug abuse;
  14. Pregnant women, breastfeeding women, or women of childbearing age planning to conceive; or female participants of childbearing potential and male participants (whose partners are women of childbearing potential) who do not agree to voluntarily use effective contraception from screening to 3 months after the last dose;
  15. Individuals with cognitive impairment unable to provide fully informed consent;
  16. Individuals positive for hepatitis B surface antigen, HIV antibody, hepatitis C antibody, or syphilis treponemal antibody;
  17. Individuals who have participated in another clinical trial within the past month;
  18. Individuals known to have familial colorectal cancer syndrome;
  19. Individuals who, in the opinion of the investigator, have other factors making them unsuitable for inclusion.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Quadruplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Chang Ji'an capsule group
Chang Ji'an Capsules, 4 capsules each time, 3 times a day, orally
Droga: Chang Ji'an capsule
The prescription consists of 13 medicinal ingredients including Radix Paeoniae Alba, Rhizoma Atractylodis Macrocephalae (processed), and Radix Astragali.
Comparatore placebo: Placebo group
Chang Ji'an Capsules mimic, 4 capsules per dose, 3 times a day, orally
Droga: Chang Ji'an capsule mimic
Mock capsules with "no pharmaceutically active ingredients", identical to the Chang Ji'an capsule in color, odor and appearance.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Response rate of diarrhea (stool characteristics) at the end of 8 weeks of treatment
Lasso di tempo: Evaluation will be performed at Day 56.
Proportion of subjects who met the following criteria for at least 50% of the period from randomization to the end of Week 8 of treatment: patients with a reduction of at least 50% from baseline in the number of days per week with at least one stool that has a consistency of Type 6 or 7 Bristol Stool Score compared with baseline, and abdominal pain, abdominal distension and abdominal discomfort are unchanged or improved in comparison with baseline.
Evaluation will be performed at Day 56.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
The abdominal pain response rate at the end of treatment weeks 2, 4, 6 and 8
Lasso di tempo: Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Proportion of subjects who satisfy the following criteria in no less than 50% of the treatment period from randomization to week endpoint: patients who experience a decrease in the weekly average of worst abdominal pain in the past 24 hours score of at least 30 percent compared with baseline, and the number of days per week with at least one stool with consistency of Type 6 or 7 that is the same as baseline or decreased and the number of stools of Type 6 or 7 on those days remains unchanged or decreased.
Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
The response rate of diarrhea (stool form) at the end of treatment weeks 2, 4 and 6
Lasso di tempo: Evaluation will be performed at baseline and Day 14, Day 28, Day 42.
Proportion of subjects who met the following criteria for at least 50% of the period from randomization to week endpoint: patients with a reduction of at least 50% from baseline in the number of days per week with at least one stool that has a consistency of Type 6 or 7 Bristol Stool Score compared with baseline, and abdominal pain, abdominal distension and abdominal discomfort are unchanged or improved in comparison with baseline.
Evaluation will be performed at baseline and Day 14, Day 28, Day 42.
Treatment response rate at the end of treatment weeks 2, 4, 6 and 8
Lasso di tempo: Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Defined as the proportion of subjects who meet the following criteria during at least 50% of the treatment period from randomization to the week endpoint: 1.Intensity of abdominal pain, abdominal distension and abdominal discomfort: a decrease in the weekly average of worst abdominal pain, abdominal distension and abdominal discomfort in the past 24 hours score of at least 30 percent compared with baseline; 2.Stool form: 50 percent or greater reduction in the number of days per week with at least one stool that has a consistency of Type 6 or 7 compared with baseline.
Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Distention response rate at the end of treatment weeks 2, 4, 6 and 8
Lasso di tempo: Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Proportion of subjects who satisfy the following criteria in no less than 50% of the treatment period from randomization to week endpoint: patients who experience a decrease in the weekly average of worst abdominal distention in the past 24 hours score of at least 30 percent compared with baseline, and the number of days per week with at least one stool with consistency of Type 6 or 7 that is the same as baseline or decreased and the number of stools of Type 6 or 7 on those days remains unchanged or decreased.
Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Response rate of abdominal discomfort at the end of 2, 4, 6, and 8 weeks of treatment
Lasso di tempo: Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Proportion of subjects who satisfy the following criteria in no less than 50% of the treatment period from randomization to week endpoint: patients who experience a decrease in the weekly average of worst abdominal discomfort in the past 24 hours score of at least 30 percent compared with baseline, and the number of days per week with at least one stool with consistency of Type 6 or 7 that is the same as baseline or decreased and the number of stools of Type 6 or 7 on those days remains unchanged or decreased.
Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Changes in the number of days with diarrhea in the past week compared to baseline at the end of 2, 4, 6, and 8 weeks of treatment
Lasso di tempo: Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Among patients with unchanged or improved intensity of abdominal pain, abdominal distension and abdominal discomfort, the change from baseline in the number of days with Bristol Stool Form Scale type 6 or 7 at least once during the week.
Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Changes in the average number of diarrhea episodes in the past week compared to baseline at the end of 2, 4, 6, and 8 weeks of treatment
Lasso di tempo: Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Defined as the change from baseline in the weekly frequency of Bristol Stool Form Scale Type 6 or 7 stools divided by 7 days, among patients whose intensity of abdominal pain, abdominal distension, and abdominal discomfort remained unchanged or improved.
Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Changes in Urgency Numeric Rating Scale(Likert 5 point scale, score range:0-4, Lower-is-Better endpoint) compared to baseline at the end of weeks 2, 4, 6, and 8, and in the past 2 weeks
Lasso di tempo: Evaluation will be performed at baseline and D14, D28, D42, D56.
Assessed based on the change in defecation urgency score.
Evaluation will be performed at baseline and D14, D28, D42, D56.
Changes from baseline in IBS Symptom Severity Score (IBS-SSS, score range:0-500, Lower-is-Better endpoint) at the end of 2, 4, 6, and 8 weeks of treatment.
Lasso di tempo: Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Assessed by the changes in scores of the IBS-SSS scales.
Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Changes from baseline in Quality of Life scale score (IBS-QOL, score range:0-136, Lower-is-Better endpoint) at the end of 2, 4, 6, and 8 weeks of treatment.
Lasso di tempo: Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Assessed by the changes in scores of the IBS-QOL scales.
Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Changes from baseline in Traditional Chinese Medicine syndrome score at the end of treatment weeks 2, 4, 6 and 8.
Lasso di tempo: Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Assessed by the changes in Traditional Chinese Medicine (TCM) syndrome scores.
Evaluation will be performed at baseline and Day 14, Day 28, Day 42, Day 56.
Proportion of subjects with sustained remission and no worsening of diarrhea severity at Week 4 and Week 8 during the follow-up period.
Lasso di tempo: Evaluations will be performed at baseline, 4 and 8 weeks of the follow-up period after the end of treatment.
Assessed via the Likert scale(Likert 7 point scale, score range:1-7, Lower-is-Better endpoint) completed in ePRO.
Evaluations will be performed at baseline, 4 and 8 weeks of the follow-up period after the end of treatment.
Proportion of subjects without diarrhea associated with diarrhea-predominant irritable bowel syndrome at follow-up Week 4 and Week 8.
Lasso di tempo: Evaluations will be performed at Day 7, Day 14, Day 21, Day 28, Day 35, Day 42, Day 49, Day 56 after treatment completion.
Assessed via the Likert scale(Likert 7 point scale, score range:1-7, Lower-is-Better endpoint) completed in ePRO.
Evaluations will be performed at Day 7, Day 14, Day 21, Day 28, Day 35, Day 42, Day 49, Day 56 after treatment completion.
Usage of rescue medication
Lasso di tempo: Evaluations shall be conducted at Week 8 of treatment.
Statistical analysis will be performed based on the consumption of rescue medication throughout the entire trial period.
Evaluations shall be conducted at Week 8 of treatment.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Beijing Hospital of Traditional Chinese Medicine

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

31 maggio 2026

Completamento primario (Stimato)

31 gennaio 2028

Completamento dello studio (Stimato)

31 maggio 2028

Date di iscrizione allo studio

Primo inviato

17 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

22 maggio 2026

Primo Inserito (Effettivo)

28 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

28 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

22 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • FA-CJA-III-2510

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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Condizioni

Malattie rare

Interventi farmacologici

Supplementi dietetici

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Sedi

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