The Second Affiliated Hospital of Nanjing Medical University
Nanjing, Jiangsu, 210011, China
Location status: Recruiting
NCT Number: NCT07767370
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
Interested in participating?
Request Info18 year–75 year
All sexes
Interventional
Early Phase 1
Nanjing, Jiangsu, 210011, China
Location status: Recruiting
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
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).
Exclusion criteria
Exclusion criteria
related to chronic diarrhoea
Drug-related exclusion criteria
Other gastrointestinal exclusion criteria
Take 4 melesalazine capsules each time, 3 times a day. Continue for 14 days.
Take 1 ND-12 capsule and 3 blank capsules each time, 3 times a day. Continue for 14 days
Take 1 ND-12 capsule and 3 H-6 capsules each time, 3 times a day. Continue for 14 days
Time frame: 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
Time frame: 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)
Time frame: 14 days post-drug administration
The proportion of subjects achieving deep remission on the 14th day (Fecal calprotectin < 100 μg/g)
Time frame: 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
Time frame: 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;
Time frame: 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;
Time frame: 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
Time frame: baseline, 7 days post-drug administration
Changes in the gut microbiome and metabolome of subjects on the 7th day compared with baseline
Contact information is provided by the study sponsor or research team.
The Second Hospital of Nanjing Medical University
Other
A Randomised, Controlled, Double-blind Exploratory Study of ND-12 Combined With H-6 in the Treatment of Adult Chronic Inflammatory Diarrhea
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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