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ND-12 Combined With H-6 for Adult Chronic Inflammatory Diarrhea

11 augusti 2026 uppdaterad av: Faming Zhang, The Second Hospital of Nanjing Medical University

A Randomised, Controlled, Double-blind Exploratory Study of ND-12 Combined With H-6 in the Treatment of Adult Chronic Inflammatory Diarrhea

This is a randomized controlled trial to explore the efficacy and safety of ND-12 combined with H-6 for patients with chronic inflammatory diarrhea

Studieöversikt

Detaljerad beskrivning

At least 36 subjects who meet all the inclusion criteria but do not meet any exclusion criteria will be enrolled in this study. They will be randomly assigned to the mesalazine group , ND-12, and the ND-12/H-6 group. Data of demographic characteristics, intestinal symptoms, medicine treatment usage and clinical outcomes will be collected. After treatment, they will enter the follow-up period for efficacy and safety evaluation.

Studietyp

Interventionell

Inskrivning (Beräknad)

36

Fas

  • Tidig fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studieorter

    • Jiangsu
      • Nanjing, Jiangsu, Kina, 210011
        • Rekrytering
        • The Second Affiliated Hospital of Nanjing Medical University
        • Kontakt:

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Nej

Beskrivning

Inclusion Criteria:

  1. Subjects aged 18-75 years (inclusive), of any gender.
  2. Meet any one of the following conditions:

1) Previously diagnosed ulcerative colitis, currently in the active phase; 2) Diagnosis of chronic diarrhoea: stool frequency ≥3 times per day or markedly higher than the subject's usual baseline; disease duration >4 weeks; recurrent diarrhoea with an interval of 2-4 weeks between episodes; loose stools (Bristol Stool Form Scale type 5, 6, or 7).

3. Faecal calprotectin >150 μg/g. 4.The subject or their legal representative provides informed consent by voluntarily signing the informed consent form, fully understands the study objectives, maintains effective communication with investigators, and is capable of understanding and complying with all requirements specified in this study protocol.

Exclusion Criteria:

Exclusion criteria related to chronic diarrhoea

  1. Presence of any of the following symptoms:

    1. Fever ≥37.5°C;
    2. Moderate-to-severe dehydration requiring intravenous fluid replacement;
    3. Recurrent vomiting.
  2. Diarrhoea caused by enteric pathogens (e.g., Clostridioides difficile, Salmonella typhi, etc.).
  3. Underlying diseases that may trigger diarrhoea, including hyperthyroidism, gastrointestinal autonomic nervous dysfunction, gastrointestinal malignancy, Crohn's disease, history of colectomy (appendectomy, haemorrhoid surgery and fistula-in-ano surgery excluded), history of small-bowel resection (>20 cm of resected intestinal segment), etc.

    Drug-related exclusion criteria

  4. Suspected drug-induced diarrhoea (e.g., long-term use of laxatives, antibiotics, chemotherapeutic agents, etc.) where discontinuation of the offending drug is not feasible.
  5. History of allergy to any component of mesalazine capsules, ND-12 capsules or H-6 capsules.
  6. Anticipated need for prohibited medications during the study (e.g. antibiotics, antidiarrhoeals, antiemetics, antispasmodics, etc.).
  7. Use of any investigational drug within 30 days prior to enrolment into this study.

    Other gastrointestinal exclusion criteria

  8. History of gastrectomy or vagotomy.
  9. Known malabsorptive disorders include coeliac disease.
  10. Known lactose intolerance.
  11. Any suspected condition requiring abdominal surgery. Other exclusion criteria
  12. Confirmed human immunodeficiency virus (HIV) positive status, known or suspected immunosuppression.
  13. Known severe hepatic or renal insufficiency.
  14. Past or current history of alcohol abuse and/or known substance abuse (cocaine, heroin, cannabis, etc.).
  15. Any psychiatric condition impairing the subject's ability to understand the nature, scope and potential consequences of the study, and/or documented evidence of non-cooperation.
  16. Pregnant or lactating women.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Trippel

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Mesalazine
Eligible subjects meeting all inclusion criteria and none of the exclusion criteria randomized to this sequence will receive Mesalazine interventions at three separate time points over one day
Take 4 melesalazine capsules each time, 3 times a day. Continue for 14 days.
Experimentell: ND-12
Eligible subjects meeting all inclusion criteria and none of the exclusion criteria randomized to this sequence will receive ND-12 interventions at three separate time points over one day
Take 1 ND-12 capsule and 3 blank capsules each time, 3 times a day. Continue for 14 days
Experimentell: ND-12/H-6
Eligible subjects meeting all inclusion criteria and none of the exclusion criteria randomized to this sequence will receive ND-12 and H-6 interventions at three separate time points over one day
Take 1 ND-12 capsule and 3 H-6 capsules each time, 3 times a day. Continue for 14 days

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Fecal calprotectin of patients 14 days after treatment compared to the baseline level
Tidsram: baseline, 14 days post-drug administration
The rate of change in fecal calprotectin levels of the subjects at 14 days compared to the baseline level
baseline, 14 days post-drug administration

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
The proportion of subjects who achieved a clinical response on the 14th day
Tidsram: 14 days post-drug administration
The proportion of subjects who achieved a clinical response on the 14th day(Fecal calprotectin decreased by ≥50% compared to the baseline or returned to normal <150 μg/g)
14 days post-drug administration
The proportion of subjects achieving deep remission on the 14th day
Tidsram: 14 days post-drug administration
The proportion of subjects achieving deep remission on the 14th day (Fecal calprotectin < 100 μg/g)
14 days post-drug administration
Serum inflammatory factors after treatment
Tidsram: baseline, 14 days post-drug administration
The changes in inflammatory factors (IL-1β, IL-10, TNF-α) in the blood of the subjects at 14 days compared to the baseline level
baseline, 14 days post-drug administration
The frequency of defecation after treatment
Tidsram: baseline, 7 days post-drug administration, 14 days post-drug administration, and 28 days post-drug administration
The situation of the subjects' defecation frequency on the 7th, 14th, and 28th days compared to the baseline;
baseline, 7 days post-drug administration, 14 days post-drug administration, and 28 days post-drug administration
The fecal consistency scores after treatment
Tidsram: baseline, 7 days post-drug administration, 14 days post-drug administration, and 28 days post-drug administration
The changes in the fecal consistency scores (measured using the Bristol Fecal Form Scale) of subjects on the 7th, 14th, and 28th days compared to the baseline;
baseline, 7 days post-drug administration, 14 days post-drug administration, and 28 days post-drug administration
The gastrointestinal symptom grading scores after treatment
Tidsram: baseline, 7 days post-drug administration, 14 days post-drug administration, and 28 days post-drug administration
The gastrointestinal symptom grading scores (using the GSRS scoring scale) of subjects on the 7th, 14th, and 28th days compared with the baseline values
baseline, 7 days post-drug administration, 14 days post-drug administration, and 28 days post-drug administration
The changes of gut microbiome and metabolome
Tidsram: baseline, 7 days post-drug administration
Changes in the gut microbiome and metabolome of subjects on the 7th day compared with baseline
baseline, 7 days post-drug administration

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Allmänna publikationer

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

20 juli 2026

Primärt slutförande (Beräknad)

31 augusti 2028

Avslutad studie (Beräknad)

31 augusti 2028

Studieregistreringsdatum

Först inskickad

11 augusti 2026

Först inskickad som uppfyllde QC-kriterierna

11 augusti 2026

Första postat (Faktisk)

17 augusti 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

17 augusti 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

11 augusti 2026

Senast verifierad

1 augusti 2026

Mer information

Termer relaterade till denna studie

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