跳至主要内容
临床试验/NCT04687358
NCT04687358进行中(未招募)不适用

Registry of the Natural History of Recurrent Pericarditis in Pediatric and Adult Patients

Kiniksa Pharmaceuticals International, plc29 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2021年3月16日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
500
试验地点
29
主要终点
Patients using 1 or more RP treatments

研究概览

简要总结

The registry will focus on furthering the understanding of the natural history of recurrent pericarditis (RP), as well as document RP-related clinical, health-related quality of life (HRQoL), and economic burden and will assist the medical community to refine or develop data-driven recommendations for clinical management of RP patients to optimize clinical outcomes. It also aims to generate data in support of the impact of rilonacept on clinical outcomes in a real-world population.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

入排标准

年龄范围
7 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •ACTIVE RP PATIENTS
  • •Select Inclusion Criteria:
  • •Physician-confirmed (or confirmation in medical records) diagnosis of RP defined as an initial, acute, episode and at least one pericarditis recurrence after the initial acute episode
  • •Experienced at least one pericarditis episode in the 3 years prior to inclusion
  • •Under the care of a physician for the treatment and management of RP
  • •Currently prescribed medication for RP

排除标准

  • •Diagnosis of pericarditis secondary to tuberculosis (TB), cancer if not in full remission, post thoracic blunt trauma (e.g., motor-vehicle accidents), myocarditis, systemic autoimmune diseases, except SJIA and adult Still's disease, HIV
  • •Appears to have an impairment (e.g., cognitive, hearing, visual) or insufficient English or Spanish proficiency that could interfere with ability to complete patient-completed assessments
  • •Currently enrolled in a therapeutic investigational drug or device study
  • •INACTIVE RP PATIENTS
  • •Select Inclusion Criteria:
  • •Physician-confirmed (or confirmation in medical records) diagnosis of RP defined as an initial, acute, episode and at least one pericarditis recurrence after the initial, acute episode
  • •Patient had a last episode occurring at least 3 years and up to 5 years before registry inclusion
  • •Resolution of RP symptoms confirmed with no further RP treatment for 3 years prior to registry enrollment
  • •Select Exclusion Criteria:
  • •Experienced a pericarditis episode within 3 years from enrolling in the registry
  • •Currently receiving RP treatment prescribed by a treating physician (e.g., CS, colchicine)
  • •Diagnosis of pericarditis secondary to tuberculosis (TB), cancer if not in full remission, post thoracic blunt trauma (e.g., motor-vehicle accidents), myocarditis, systemic autoimmune diseases except SJIA and adult Still's disease, HIV
  • •Enrolled in a therapeutic investigational clinical trial during the observation period

研究组 & 干预措施

Active RP

Patients who are currently under the care of a physician for treatment of RP, currently on treatment for RP, and have had an episode (recurrence of typical pericarditis pain associated with supportive objective evidence of pericarditis) in the last 3 years prior to enrollment. Once included in the registry, these patients will have both retrospective and prospective follow-up and data collection (hybrid design).

Inactive RP

Patients who have had a diagnosis of RP, have not had an episode for 3 years and have not been prescribed any treatment for RP in the last 3 years, prior to enrolling in the registry. Once included in the registry, data collected from these patients will be retrospective only.

结局指标

主要结局

Patients using 1 or more RP treatments

时间窗: 5 years

Proportion of patients using 1, 2, 3, or more concomitant RP treatments

次要结局

  • Adverse event rate(5 years)
  • Change in cardiovascular magnetic resonance (CMR) imaging(5 years)
  • Changes in PROMIS-29 patient-reported outcomes(5 years)
  • Changes in PROMIS Pediatric/Parent 25 patient-reported outcomes(5 years)
  • Changes in insomnia severity index (ISI) patient-reported outcomes(5 years)
  • Change in cardiac magnetic resonance imaging (cMRI)(5 years)
  • Change in dyspnea(5 years)
  • Change in echocardiogram(5 years)
  • Change in fever(5 years)
  • Change in Multidetector (cardiac) computed tomography (MDCT)(5 years)
  • Change in C-reactive protein (CRP)(5 years)
  • Change in interleukin-1 (IL-1)(5 years)
  • Change in chest x-ray(5 years)
  • Changes in Patient Global Impression of Pericarditis Severity (PGIPS) patient-reported outcomes(5 years)
  • Change in interleukin-6 (IL-6)(5 years)
  • Most frequently used RP treatments(5 years)
  • Reduction in the use of corticosteroids(5 years)
  • Change in RP activity(1 year)
  • Change in pericardial rub(5 years)
  • Change in pericardial effusion(5 years)
  • Change in erythrocyte sedimentation rate (ESR)(5 years)
  • Change in white blood count (WBC)(5 years)
  • Change in electrocardiogram (ECG)(5 years)
  • Changes in persistent pericarditis numerical rating scale (PPNRS) patient-reported outcomes(5 years)
  • Changes in D12 patient-reported outcomes(5 years)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (29)

Loading locations...

相似试验

Unknown
不适用
RAHM Foundation Retrospective Study of Various DiseasesPain, Spinal Surgeries, Hip and Knee Joint Replacement, Adverse Events
NCT02359786Rahm Foundation10,000
终止
不适用
Prospective, Observational Registry of Renaissance-guided Spine SurgeriesDegenerative Spine DiseaseSpinal Deformity
NCT02212899Mazor Robotics93
进行中(未招募)
不适用
PROPEL - A Prospective Observational Patient Registry to Evaluate ENPP1 and ABCC6 DeficiencyEctonucleotide Pyrophosphatase/Phosphodiesterase 1 DeficiencyATP-Binding Cassette Subfamily C Member 6 Deficiency
NCT06302439Inozyme Pharma54
招募中
不适用
Prospective Recurrent Pregnancy Loss RegistryRecurrent Pregnancy Loss
NCT05989178University of British Columbia3,000
招募中
不适用
Natural History Study for Charcot Marie Tooth DiseaseCharcot-Marie-Tooth Disease Type 2A2ACharcot-Marie-Tooth Disease Type 2L (Diagnosis)HNPPCharcot Marie Tooth Disease (CMT)Charcot-Marie-Tooth Disease and DeafnessCharcot-Marie-Tooth Disease Type 4HCharcot-Marie-Tooth Disease Type 2B5Charcot-Marie-Tooth Disease Type 2TCharcot-Marie-Tooth Disease Type 2RCharcot-Marie-Tooth Disease Type 2YX-Linked Charcot-Marie-Tooth DiseaseCharcot-Marie-Tooth Disease Type 2S (Disorder)Charcot-Marie-Tooth Disease Type 4CCharcot-Marie-Tooth Disease Type 1DCharcot-Marie-Tooth Disease Type 2Q (Diagnosis)Charcot-Marie-Tooth Disease Type 2A2Charcot-Marie-Tooth Disease Type 2KCharcot-Marie-Tooth Disease Type 2MCharcot-Marie-Tooth Disease Type 2PCharcot-Marie-Tooth Disease Type 4F (Diagnosis)Charcot-Marie-Tooth Disease Type 2HCharcot-Marie-Tooth Disease Type 1FCharcot-Marie-Tooth Disease Type 2DCharcot-Marie-Tooth Disease Type 4DCharcot-Marie-Tooth Disease Type 2ICharcot-Marie-Tooth Disease Type 2JCharcot-Marie-Tooth Disease Type 2ECharcot-Marie-Tooth Disease Type 2GCharcot-Marie-Tooth Disease Type 1CCharcot-Marie-Tooth Disease Type 2O (Diagnosis)Charcot-Marie-Tooth Disease Type 4B2Charcot-Marie-Tooth Disease Type 4ECharcot-Marie-Tooth Disease Type 2N (Diagnosis)Charcot-Marie-Tooth Disease Type 4B3Charcot-Marie-Tooth Disease, Type IACharcot-Marie-Tooth Disease Type 2Charcot-Marie-Tooth Disease Type 2B2Charcot-Marie-Tooth DiseaseCharcot-Marie-Tooth Disease Type 4ACharcot-Marie-ToothCharcot-Marie-Tooth Disease Type 2A1Charcot-Marie-Tooth Disease Type 4B1Charcot-Marie-Tooth Disease Type 2U (Diagnosis)Charcot-Marie-Tooth Disease Type 2B1Charcot-Marie-Tooth Disease Type 2ACharcot-Marie-Tooth Disease, Type 2CCharcot-Marie-Tooth Disease Type 2A2BCharcot-Marie-Tooth Disease, Type IBCharcot-Marie-Tooth Disease, Type 4A, Axonal Form
NCT05902351Hereditary Neuropathy Foundation10,000