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Effects of Lactulose on Gut Microbiota and Metabolism in Diabetic Constipated Patients

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• Age: 18-70 years

• Type 2 Diabetes Diagnosis (per 2017 ADA criteria), meeting ≥1 of:

‣ Fasting plasma glucose (FPG) ≥7.0 mmol/L

⁃ hour plasma glucose ≥11.1 mmol/L during 75g anhydrous oral glucose tolerance test (OGTT)

⁃ Random plasma glucose ≥11.1 mmol/L with hyperglycemia symptoms or hyperglycemic crisis

• Functional Constipation (Rome IV criteria), requiring:

‣ ≥2 of the following

• occurring in ≥25% of defecations

∙ Straining

∙ Lumpy/hard stools (Bristol Stool Scale 1-2)

∙ Sensation of incomplete evacuation

∙ Anorectal obstruction/blockage

∙ Manual maneuvers required

∙ \<3 spontaneous bowel movements/week

⁃ 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

Locations
Other Locations
China
Peking Union Medical College Hospital
RECRUITING
Beijing
Contact Information
Primary
Yaowen Hu
1440556437@qq.com
+86 18811618952
Time Frame
Start Date: 2023-07-01
Estimated Completion Date: 2026-07-30
Participants
Target number of participants: 60
Treatments
Active_comparator: Lactulose Oral Solution
Experimental: Lactulose Oral Solution+Live Combined B. Subtilis and E. Faecium Enteric-coated Capsules
Related Therapeutic Areas
Sponsors
Collaborators: Beijing Huaxin Hospital, Beijing Luhe Hospital, Beijing Huairou Hospital, Beijing Hospital
Leads: Peking Union Medical College Hospital

This content was sourced from clinicaltrials.gov

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