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| Name | Class |
|---|---|
| Beijing Hospital | OTHER_GOV |
| Beijing Huaxin Hospital | OTHER |
| Beijing Luhe Hospital | OTHER |
| Beijing Huairou Hospital |
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Constipation is the most common gastrointestinal manifestation in diabetic patients. Emerging evidence suggests that gut microbiota dysbiosis may contribute to the pathogenesis of diabetes, highlighting the need to investigate its role in diabetic constipation, though current research remains limited.
Current management of diabetic constipation primarily relies on bulk-forming and osmotic laxatives. Additionally, microbiome-modulating agents (e.g., probiotics, prebiotics, and synbiotics) may serve as adjunctive therapies by regulating gut microbiota and enhancing intestinal motility. Lactulose, a well-tolerated osmotic laxative with prebiotic effects, is widely recommended in clinical guidelines. It promotes short-chain fatty acid production, increases fecal volume, and accelerates colonic transit, thereby alleviating constipation. However, its specific impact on gut microbiota composition and metabolic pathways in diabetic constipation remains unclear.
This study aims to explore changes in fecal microbiota and metabolomic profiles in diabetic patients with chronic constipation following treatment with lactulose alone or in combination with Bacillus subtilis-Enterococcus faecium probiotics, providing mechanistic insights into prebiotic therapy for this condition.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Lactulose Oral Solution | Active Comparator |
| |
| Lactulose Oral Solution+Live Combined B. Subtilis and E. Faecium Enteric-coated Capsules | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Lactulose oral solution | Drug | Oral, 30 mL once daily administered during breakfast. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Changes in Constipation Symptom Scores Pre- and Post-Treatment | Assessment of treatment efficacy on constipation symptoms: Changes in symptom scores from baseline to post-treatment within each treatment arm and comparative analysis between the lactulose monotherapy group and lactulose+Medilac-S combination therapy group | From enrollment (0 week) to 2 weeks, and 4 Weeks at the end of treatment |
| Changes in Fecal Microbiota Composition (16S rRNA and Metagenomics) | Comparison of Fecal Microbiota Composition Changes (16S rRNA and Metagenomics): Pre- vs. Post-Treatment Alterations and Intergroup Differences Between Lactulose Monotherapy and Lactulose+Medilac-S Combination Therapy | From enrollment (0 week) to 2 weeks, and 4 Weeks at the end of treatment |
| Temporal Changes in Fecal Untargeted Metabolomics Profiles | Temporal Changes in Fecal Untargeted Metabolomics Profiles: Pre- vs. post-treatment alterations and comparative analysis between lactulose monotherapy and lactulose+Medilac-S combination groups. | From enrollment (0 week) to 2 weeks, and 4 Weeks at the end of treatment |
| Measure | Description | Time Frame |
|---|---|---|
| Changes in Fasting Blood Glucose and Glycated Albumin Levels | Changes in Fasting Blood Glucose and Glycated Albumin Levels: Pre- vs. post-treatment variations and comparative analysis between lactulose monotherapy and lactulose+Medilac-S combination groups | From enrollment (0 week) to 2 weeks, and 4 Weeks at the end of treatment |
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Inclusion Criteria:
Age: 18-70 years
Type 2 Diabetes Diagnosis (per 2017 ADA criteria), meeting ≥1 of:
Functional Constipation (Rome IV criteria), requiring:
≥2 of the following
No loose stools without laxatives
Exclusion of IBS diagnosis. Symptom duration >6 months, with active symptoms meeting criteria for last 3 months.
Stable Glycemic Control: No anticipated antidiabetic medication adjustments during study
Dietary Stability: Maintain consistent diet; avoid yogurt, fermented foods, prebiotic-containing processed foods, or other items that may confound results
Exclusion Criteria:
Secondary Constipation due to organic diseases or medication effects.
Constipation-predominant Irritable Bowel Syndrome (IBS-C).
Concurrent gastrointestinal disorders (e.g., inflammatory bowel disease, colorectal cancer).
Type 1 Diabetes Mellitus.
Severe chronic comorbidities, including:
Recent use (within 1 month) of confounding medications:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Yaowen Hu | Contact | +86 18811618952 | 1440556437@qq.com |
| Name | Affiliation | Role |
|---|---|---|
| Jingnan Li, MD, Ph.D | Peking Union Medical College Hospital | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Peking Union Medical College Hospital | Recruiting | Beijing | China |
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| ID | Term |
|---|---|
| D003920 | Diabetes Mellitus |
| D003248 | Constipation |
| ID | Term |
|---|---|
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D004700 | Endocrine System Diseases |
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| ID | Term |
|---|---|
| D007792 | Lactulose |
| ID | Term |
|---|---|
| D004187 | Disaccharides |
| D009844 | Oligosaccharides |
| D011134 | Polysaccharides |
| D002241 | Carbohydrates |
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| OTHER |
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| Live Combined B. Subtilis and E. Faecium Enteric-coated Capsules | Drug | Oral, 2 tablets (500 mg per tablet) three times daily (TID). |
|
| Changes in Blood Lipid Profiles (Total Cholesterol, Triglycerides, HDL-C, and LDL-C) |
Changes in Blood Lipid Profiles (Total Cholesterol, Triglycerides, HDL-C, and LDL-C): Pre- vs. post-treatment alterations and comparative analysis between lactulose monotherapy and lactulose+Medilac-S combination therapy groups |
| From enrollment (0 week) to 2 weeks, and 4 Weeks at the end of treatment |
| D012817 | Signs and Symptoms, Digestive |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D000073893 |
| Sugars |