ALPCO Calprotectin CLIA Assay - Measurement of Calprotectin Levels in Human Stool
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 220
- 试验地点
- 3
- 主要终点
- In vitro diagnostic value of Calprotectin
研究概览
简要总结
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.
详细描述
The clinical study serves to confirm the sensitivity and specificity of the ALPCO Calprotectin CLIA as compared to gastroenterologist diagnosis (including colonoscopy results and other clinical information) in patients with signs and symptoms of IBS or IBD, using the proposed cut-off values (50 and 100 µg/g) as both an aid in the diagnosis of Inflammatory Bowel Disease and as an aid to differentiate IBD from Irritable Bowel Syndrome. The clinical study will be conducted in compliance with applicable requirements in the protection of human subjects regulations in 21 CFR part 50, the institutional review boards regulations in 21 CFR part 56, and the investigational device exemptions regulations in 21 CFR part 812.
The goal of this clinical study is to confirm the sensitivity and specificity of the ALPCO Calprotectin CLIA in patients using the proposed cut-off value (50 µg/g) as an aid in differentiating between a diagnosis of an Inflammatory Bowel Disease and other non-inflammatory disorders, most notably Irritable Bowel Syndrome. (See Appendix I for draft study protocol). Final assay cut-off will be determined upon completion of analytical studies and product validation.
Calprotectin values greater than 50 µg/g (or defined assay cut-off) are indicative of neutrophil infiltrate in the gastrointestinal tract, and therefore signal the presence of an active Inflammatory Bowel Disease. Calprotectin concentrations below this value do not indicate inflammation, but do not eliminate a potential diagnosis of Irritable Bowel Syndrome. Therefore, clinical use of the ALPCO Calprotectin CLIA can generate crucial data to determine whether or not a patient should undergo more invasive testing to diagnose the presence of an Inflammatory Bowel Disease. This clinical study will seek to confirm this conclusion by estimating the predictive value of positive and negative tests using the proposed cut off value in patients referred for diagnostic evaluation with signs and symptoms suggestive of either IBD or IBS.
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.
This study will be performed at multiple clinical recruiting sites with a minimum of 3 analytical test sites - ALPCO would be one test site and could test all samples from collection sites only at which endoscopies (colonoscopy) focusing on the diagnosis of bowel inflammation are performed. Patients will be enrolled in the study based on inclusion/exclusion defined criteria.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 22 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Male or female, ≥22 years of age (adults)
- •Suspected inflammatory bowel disease or irritable bowel syndrome with symptoms such as abdominal pain, diarrhea, altered appetite, weight loss, or anemia
- •Able to provide a sample according to the sampling protocol within 72-24 hours prior to the scheduled diagnostic endoscopy or 3-30 days after the colonoscopy.
- •Able to understand the study and the tasks required and sign the ICF
排除标准
- •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)
- •IBD patients receiving chemotherapy or systemic immunosuppressive drugs without completing an 8-week washout period
- •IBD patients who have previously diagnosed 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 a surgical resection or diversion procedure.
- •Known upper Gl disease such as esophagitis or gastritis that might influence the study test's ability to detect intestinal inflammatory disease
- •Have taken NSAIDS (including aspirin) on 7 or more days during the 2 weeks before providing the sample
- •Samples are not collected according to sampling protocol.
- •Any condition that in the opinion of the investigator should preclude participation in the study.
- •Using an IRB approved consent form, all study participants will be advised of study requirements and potential risks associated with study participation.
研究组 & 干预措施
IBD
Adult subjects diagnosed with IBD via endoscopy and histological findings.
干预措施: ALPCO Calprotectin CLIA (Device)
IBS
Adult subjects with IBS as per the Rome IV criteria.
干预措施: ALPCO Calprotectin CLIA (Device)
Other GI Disorders
Adult subjects with gastrointestinal disorders not meeting the Rome IV criteria or IBD diagnosis.
干预措施: ALPCO Calprotectin CLIA (Device)
Healthy Subjects
Adult subjects without any gastrointestinal complaints.
干预措施: ALPCO Calprotectin CLIA (Device)
结局指标
主要结局
In vitro diagnostic value of Calprotectin
时间窗: Through study completion, up to 52 weeks.
Value of calprotectin measurement using the ALPCO Calprotectin CLIA on the chemiluminescent automated KleeYa instrument.
次要结局
未报告次要终点