Pragmatic Clinical Trials in Scleroderma
试验速览
- 阶段
- 不适用
- 入组人数
- 400
- 试验地点
- 2
- 主要终点
- Diarrhea visual analog scale
研究概览
简要总结
Systemic Sclerosis (SSc) is an autoimmune connective tissue disease characterized by autoantibodies, fibrosis and microvascular injury and endothelial cell activation that results in vascular damage. Vascular injury induces both innate and acquired immune responses resulting in fibroblast activation and organ fibrosis. SSc may target multiple organs, including: skin, lungs, heart, vascularization, kidneys, the gastrointestinal tract and musculoskeletal structures. Mortality among scleroderma patients is significant, with a 3.5 standardized mortality ratio (SMR) in studies of prevalent cases. This mortality may be increased in the early years of the disease, reaching a SMR of 4 in a multinational inception cohort. In general, treatment strategies target involved organs as early as possible to avoid damage. Many treatment options are available for each manifestation, but evidence with respect to the order of treatment is scarce. Financial costs, the lack of proper outcome measures, difficulty to recruit patients as a rare disease, all prevent the development of new big clinical trials, oppositely to other common diseases such as stroke or cancer. The heterogeneous features of SSc may make trials challenging. The current guidelines available are the British guidelines (2017) , and the updated European League Against Rheumatism (EULAR) guidelines, published in 2017. Management guidelines have some gaps regarding second-line treatment, combinations and there are no proposed algorithms.
With the pragmatic trials, the investigators intend to fill the gap between the complicated randomized clinical trials and the observational studies. Using the treatments that have already been proved useful in SSc, in an open-label randomized way and based on some refined expert-made algorithms, will allow the investigators to establish the order in how to use them.
Patients will be offered to participate with the collection of their clinical data and, if they give their consent, they will be randomized according to the algorithms. There will be an optional part of the study consisting in the collection of blood samples and skin samples for future research.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Sequential
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Any patient with an age >18 years meeting the 2013 SSc classification criteria managed at the Rheumatology division, St. Joseph's Healthcare London.
- •Patients who refuse to be randomized for treatments but wish to provide their data for the registry will also be included, after signing the informed consent form.
排除标准
- •Refusal to participate or to sign an informed consent form.
研究组 & 干预措施
Bacterial overgrowth
干预措施: Bacterial overgrowth algorithm (Other)
Constipation
干预措施: Constipation algorithm (Other)
Skin involvement
干预措施: Skin involvement algorithm (Other)
Pain
干预措施: Pain algorithm (Other)
Interstitial lung disease induction
干预措施: Interstitial lung disease induction algorithm (Other)
Pulmonary arterial hypertension
干预措施: Pulmonary arterial hypertension algorithm (Other)
Raynaud's phenomenon
干预措施: Raynaud's phenomenon algorithm (Other)
Digital ulcers
干预措施: Digital ulcer algorithm (Other)
Inflammatory arthritis
干预措施: Inflammatory arthritis algorithm (Other)
Gastroesophageal reflux
干预措施: Gastroesophageal reflux algorithm (Other)
结局指标
主要结局
Diarrhea visual analog scale
时间窗: 3 months
Diarrhea visual analog scale variation ranging from 0 to 100 mm (0 no diarrhea, 100 very intense diarrhea)
Modified Rodnan skin score
时间窗: 1 year
Modified Rodnan skin score variation. Ranging from a total of 0 (no induration) to 51 (maximum induration)
Raynaud's phenomenon visual analog scale
时间窗: 3 months
Raynaud's phenomenon visual analog scale variation ranging from 0 to 100 mm (0 no Raynaud's phenomenon, 100 very intense Raynaud's phenomenon)
Time to the development of a new digital ulcer
时间窗: 1 year
Time to the development of a new digital ulcer
Disease activity score 28
时间窗: 3 months
Disease activity score 28 accounting for tender and swollen joints over 28 possible joints. Values \<2.6 remission, values \<3.2 low disease activity, values \>5.1 high disease activity
Forced vital capacity %
时间窗: 1 year
Variation of the forced vital capacity %
GERD-HRQL
时间窗: 3 months
Variation of the Gastro-esophageal reflux disease-health related quality of life questionnaire, ranging from 0 (no symptoms) to 75 (worst symptoms)
Constipation visual analog scale
时间窗: 3 months
constipation visual analog scale variation ranging from 0 to 100 mm (0 no constipation, 100 very intense constipation)
Pain visual analog scale
时间窗: 3 months
Pain visual analog scale variation, ranging from 0 to 100 mm (0 no pain, 100 very intense pain)
Bleeding
时间窗: 1 year
Documentation of bleeding
Time to the healing of a digital ulcer
时间窗: 1 year
Time to the healing of a digital ulcer
次要结局
未报告次要终点
研究者
Andreu Fernandez Codina
Principal investigator
University of Western Ontario, Canada
