Individualization of Oral Mesalazine Treatment Through a Self-managed Web-based Solution in Mild-to-moderate Ulcerative Colitis: A Pilot Study
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 发起方
- 入组人数
- 1
- 试验地点
- 1
- 主要终点
- Change in Total Inflammation Burden Scoring (TIBS)
研究概览
简要总结
This study investigates the effect of individualized monotherapy with Mesalazine (Pentasa Sachet ®) on time to remission in patients with mild to moderate UC in an eHealth setting.
详细描述
More than 3 million Europeans suffer from inflammatory bowel disease (IBD), where Crohn's Disease (CD) and Ulcerative Colitis (UC) are the most common forms. They are chronic, relapsing and remitting diseases resulting in uncontrolled inflammation of the gastrointestinal (GI) tract with symptoms of diarrhoea, abdominal pain, weight loss and blood in the stools. The treatment aims to relieve and prevent GI tract inflammation and consists of anti-inflammatory and immunosuppressive drugs or surgical removal of the colon as a final option. The main treatment option for mild to moderate UC is Aminosalicylate. Mesalazine (5-aminosalicylic acid), both orally and topically, has been proven to be an effective treatment option for inducing as well as maintaining remission in patients with UC.
Pentasa Sachet are Mesalazine micro granules coated in ethyl cellulose with high (95%) 5-aminosalicylic acid (5-ASA) load. The coating provides a prolonged release of Mesalazine, allowing a continuous action from small bowel to rectum. Approximately 75% of the micro granules are released in the colon. This reduces the number of applications needed per day and is therefore considered to be a more desirable option by the patients. Once daily administrated 5-aminosalicylic acid (5-ASA) has been shown to be as effective as conventional dosing.
Fecal Calprotectin (FC) is an accurate biomarker of GI tract inflammation. FC correlates well with endoscopic disease activity and consequently serves as a substitute marker for mucosal healing as well as a clinical tool for disease monitoring. A home testing kit with a smart phone application, which only takes 18 min to carry out, has been developed. Thereby, facilitating the opportunity of telemonitoring of the disease course and stimulating patient engagement, empowerment and adherence to treatment.
Medication adherence is essential for maintaining remission, since non-adherence is one of the main causes of disease activity. A combined therapy of oral and topical 5-ASA is recommended by current guidelines for the treatment of active mild to moderate UC. However, patient adherence to oral 5-ASA is poor (approximately 60%), and even poorer to topical therapy (approximately 32%). A previous eHealth trial on individualized oral 5-ASA therapy reported higher adherence rates than previous studies on standard care. In addition, 90% of the study patients responded with remission on monotherapy and only 10% needed a combined therapy with topical treatment.
Web-based treating solutions (eHealth) have shown to optimize treatment effect in chronic diseases such as asthma, type 1 diabetes, and coagulation diseases. A web-based treatment solution for IBD patients, Constant-care, was in 1997 launched by Dr. Pia Munkholm. The web-program has since been proven to be an effective clinical tool, resulting in enhanced compliance, empowerment, improved quality of life and decreased relapse duration in IBD patients. Constant-Care consists of an education package and a disease-monitoring package. The disease monitoring part of the program is built upon an algorithm of two variables; FC and a validated disease activity questionnaire, Simple Clinical Colitis Activity Index (SCCAI) for UC patients. The FC values are acquired by the patients through a home testing kit and the disease activity questionnaire is filled out by the patients in the web- program. The eHealth system cumulates the data immediately, and subsequently presenting the result, a Total inflammatory Burden Score (TIBS), to the patients as a visual "traffic light" indicator of disease activity. Patients receive treatment advices by the program depending on the severity of the disease: green- remission, yellow- moderate activity, red-severe activity.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 75 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Fulfil the Copenhagen Diagnostic criteria for UC
- •Age between 18 and 75 years
- •New and relapse patients diagnosed with Mild-to-moderate UC
- •Current relapse (minimum 1 out of 2) SCCAI>2 (with a positive score in the variable of blood in stool) FC ≥200
- •Diagnosed with left sided or extensive UC(24)
- •Understand written and spoken Danish
- •Easy access to internet and smartphone
排除标准
- •Evidence of enteric infection
- •Treatment with immunomodulators such as steroids, azathioprine, methotrexate, or infliximab within the last 8 weeks
- •Two or more courses of oral steroids in the past 12 months
- •Diagnosed with proctitis
- •Severe disease activity (SCCAI >6 or FC ≥600)
结局指标
主要结局
Change in Total Inflammation Burden Scoring (TIBS)
时间窗: At baseline and at 12 weeks or until remission, which ever comes first
Self reported disease activity in combination with a fecal biomarker of inflammation (fecal calprotectin) results in TIBS. Disease activity is scored by 6 questions yielding: remission (\<3) , mild to moderate disease activity (3-4) and severe disease activity ( \>5). Fecal calprotectin: remission (\<200mg/kg ), mild to moderate (200-599 mg/kg ), severe (\>599 mg/kg). The two items are added together in a weighted manner giving the Total inflammation burden scoring (TIBS): remission (0-8), mild to moderate (9-32), severe (33-99).
次要结局
- Compliance with medication(at baseline and after 12 weeks)
- Disease course type(At baseline and after 12 weeks)
- Short Inflammatory Bowel Disease Questionnaire(at baseline and after 12 weeks)
- Disability(at baseline and after 12 weeks)
- Fatigue(at baseline and after 12 weeks)
研究者
Petra Weimers
Prinicipal Investigator
Nordsjaellands Hospital
