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ALPCO Calprotectin CLIA Assay - Measurement of Calprotectin Levels in Human Stool
Who can join
Ages 22 and older · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion criteria: * Male or female, ≥22 years of age (adults) * Subjects with suspected inflammatory bowel disease or irritable bowel syndrome presenting one or more of the following symptoms: abdominal pain, diarrhea, altered appetite, anemia, or unexpected weight loss. Not all symptoms are required; clinical presentation must support suspicion of inflammatory bowel disease or irritable bowel syndrome in the investigator's opinion. * Able to provide a sample either within 14 days before beginning bowel preparation for the scheduled colonoscopy, or between 3 and 14 days after the colonoscopy. * Able to understand the study and the tasks required and sign the ICF Exclusion Criteria * Unable or unwilling to provide a stool specimen * Known active intestinal cancer or in remission with abnormal levels (per physician assessment) * Known active intestinal infection or history of treated intestinal infection with persistent abnormal levels (per physician assessment) * Subjects receiving chemotherapy or systemic immunosuppressive drugs without completing an 8-week washout period IBD patients who have previously diagnosed with IBD managed with immunomodulators, 5-ASA or biologic therapies without completing an 8-week washout period for biologics and immunomodulators or 4 weeks for 5-ASA * IBD patients who have previously been diagnosed with IBD and have undergone surgical resection or diversion procedure. * Current or active upper gastrointestinal disease (e.g., esophagitis, gastritis, GERD, or acid reflux) with ongoing symptoms or requiring active treatment. * Use of proton pump inhibitors (PPIs) or H2-receptor antagonists within the 2 weeks prior to providing the stool sample. * Use of NSAIDs, including aspirin, on seven or more days within the 14 days prior to sample collection. * Samples are not collected according to sampling protocol. * Any condition that in the opinion of the investigator should preclude participation in the study.
About the study
The ALPCO Calprotectin CLIA is an in vitro diagnostic test intended to quantitatively measure concentrations of fecal calprotectin in human stool samples. Calprotectin is a protein biomarker of mucosal inflammation. Measurement of calprotectin can aid in the diagnosis of Inflammatory Bowel Diseases (IBD), specifically Crohn's Disease (CD) and Ulcerative Colitis (UC), as well as aid in the differentiation of IBD from Irritable Bowel Syndrome (IBS) when used in conjunction with other diagnostic testing and the total clinical picture. The goal of the study is to generate data to support positive and negative predictive value of the ALPCO Calprotectin assay in patients with signs and symptoms of IBS or IBD.
What is being tested
- ALPCO Calprotectin CLIA (device)
Sponsor: American Laboratory Products Company · Participants: 1,000 · Started: Mar 25, 2025
Contact the study team
- Yomi Ojutalayo · Phone: 800-592-5726
- Jim Richard · Phone: 800-592-5726
Official record on ClinicalTrials.gov — NCT06810518
Locations in the U.S.
| Florida | Med-Care Research Corp, Miami |
| New Hampshire | ALPCO, Salem (Not yet recruiting) |
| Ohio | Gastro Intestinal Research Institute of Northern Ohio,, Westlake |
Conditions
From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.