About this trial
The study is intended to find a new trusted, cost-effective biomarker for differentiating irritable bowel syndrome from inflammatory bowel disease to decrease the use of unnecessary invasive methods in patients with irritable bowel syndrome
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Adults (≥18 years) presenting with chronic lower gastrointestinal symptoms, such as diarrhea, abdominal pain, or altered bowel habits, for a duration exceeding 6 weeks.
Patients with no prior diagnosis of IBD or IBS.
Patients willing to provide informed consent and comply with study requirements.
Those without recent use of immunosuppressants or anti-inflammatory medications that could affect biomarker levels
Disqualifiers
Patients with a confirmed diagnosis of IBD and currently on treatment.
Those with acute gastroenteritis, infectious colitis, or positive stool cultures for pathogens.
Patients diagnosed with colorectal cancer, celiac disease, or other known organic GI disorders.
Recent antibiotic, NSAID, or corticosteroid use within the past 4 weeks.
Trial population
patients with lower GIT symptoms seeking medical advice at Department of Internal Medicine, Gastroenterology Outpatient Clinic, Sohag University Hospital
Trial design
Case-control
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
efficacy of myeloperoxidase for differentiating irritable bowel syndrome from inflammatory bowel disease.
Number of patients with elevated myeloperoxidase in irritable bowel syndrome and those with inflammatory bowel disease.
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: