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Research on the Application of Targeted Neutrophil Fluorescent Probes in Diseases Such as Inflammatory Bowel Disease (IBD)

lication of Targeted Neutrophil Fluorescent Probes in Diseases Such as Inflammatory Bowel Disease (IBD)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113432
Enrollment
Unknown
Registered
2025-11-28
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammatory bowel diseas

Interventions

Gold Standard:Gold Standard: endoscopic and histological examinations Reference Standard: fecal calprotectin
Index test:Small molecule fluorescent probe (MPO-RFP-B)

Sponsors

Second Affiliated Hospital of Army Medical University, PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for patients with ulcerative colitis and diarrhea-type irritable bowel syndrome: (1) Based on the diagnostic criteria in the "Chinese Guidelines for the Diagnosis and Treatment of Ulcerative Colitis (2023 · Xi'an)", combined with clinical, laboratory, imaging, endoscopic, and histopathological manifestations, a comprehensive analysis was conducted to confirm the diagnosis of inflammatory ulcerative colitis after excluding infectious and other non-infectious colitis; diagnosed as diarrhea-type irritable bowel syndrome according to the "Rome IV criteria". (2) Age 18-75 years old, gender not limited; (3) Patients need to collect feces during the treatment process for complete stool routine examination; (4) Patients can understand the research protocol and are willing to participate in this study, and provide written informed consent. Inclusion criteria for healthy volunteers: (1) Age 18-75 years old, gender not limited; (2) BMI between 18 - 28 kg/m²; (3) No systemic diseases and chronic diseases. (4) No surgical history in the past 1 year. (5) Healthy volunteers can understand the research protocol and are willing to participate in this study, agree to provide stool samples, and provide written informed consent.

Exclusion criteria

Exclusion criteria: Exclusion criteria for patients with ulcerative colitis and diarrhea-predominant irritable bowel syndrome: (1) Pregnant and lactating patients; (2) Patients with other inflammatory-related diseases; (3) Patients who have undergone progressive intestinal resection surgery, colostomy, or ileoanal pouch surgery within 3 months before enrollment; (4) Patients with clinically significant and severe, progressive or uncontrolled diseases or symptoms (including cardiovascular, neurological, mental, liver, gallbladder, kidney, blood, endocrine, etc.) in the past or currently; (5) Patients with malignant tumors; (6) Patients participating in other clinical studies. Exclusion criteria for healthy volunteers: (1) Pregnant and lactating patients; (2) Patients with a recent (<=4 weeks) history of drug use; (3) Patients who have received live vaccines within the past 1 month; (4) Patients participating in other clinical studies.

Design outcomes

Primary

MeasureTime frame
Myeloperoxidase;Fecal calprotectin;

Countries

China

Contacts

Public ContactShiming Yang

Second Affiliated Hospital of Army Medical University, PLA

13228686589@163.com+86 132 2868 6589

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026