PER-099-20招募中未知
FENOFIBRATE AS A METABOLIC INTERVENTION FOR CORONAVIRUS DISEASE 2019 (COVID-19): A RANDOMIZED CONTROLED TRIAL.
IVERSIDAD CATOLICA DE SANTA MARIA,0 个研究点目标入组 115 人开始时间: 2020年12月30日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 115
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1. Age 18 years or older.
- •2. Diagnosis of COVID-19 (of any severity), based on: (a) A clinical presentation consistent with a positive laboratory test for SARS-CoV-2 (serological test or PCR); or (b) Considered by the family medical team as a person under investigation who is undergoing laboratory tests for COVID-19, with high clinical probability, in addition to compatible pulmonary infiltrates in radiographic plaque or chest tomography (bilateral, interstitial or ground glass opacities). Inclusion will require meeting criterion (2a) only, criterion (2b) only, or both. Patients who do not have a typical acute symptomatic picture of COVID-19 should not be included.
- •3. Ability to give informed consent.
- •4. Less than 14
排除标准
- •1. Known pregnancy or lactation.
- •2. Estimated glomerular filtration rate (eGFR) 60 mL/min/1.73m2 or on dialysis (chronic renal disease stage 3-5).
- •3. History of active liver disease, cholelithiasis, hypothyroidism or rhabdomyolysis (suspected or confirmed). For purposes of the study, any history of chronic hepatopathy (including chronic hepatitis of any etiology, liver cirrhosis), recent history (last 12 months) of acute hepatitis of any etiology shall be considered as active liver disease, or in the context of COVID-19, increase in circulating AST or ALT >3 times the upper normal limit (to be performed on all patients at trial cost, unless already available in the patient within the last 72 hours). Fatty liver without hepatitis, or a remote history (>12 months) of acute viral (e.g., hepatitis A) or medication-induced hepatitis that has not progressed to chronic liver disease, do not constitute an exclusion criterion for the study.
- •4. Known hypersensitivity to fenofibrate or fenofibric acid.
- •5. Current treatment with fenofibrate, clofibrate, warfarin or other coumarinic anticoagulants, glimepiride, cyclosporine, tacrolimus.
- •6. Use of statins, except simvastatin or atorvastatin. For these 2 statins, patients taking doses >40 mg/day will be excluded.
- •8. Inability to read, write, or lack of access to a phone.
- •9. Patients with endotracheal intubation.
研究者
相似试验
进行中(未招募)
1 期
Fenofibrate for coronavirus diseaseCoronavirus disease-19MedDRA version: 23.0Level: LLTClassification code 10084381Term: Coronavirus pneumoniaSystem Organ Class: 100000004862MedDRA version: 23.0Level: LLTClassification code 10084382Term: Coronavirus disease 2019System Organ Class: 100000004862MedDRA version: 23.1Level: LLTClassification code 10084529Term: 2019 novel coronavirus infectionSystem Organ Class: 100000004862EUCTR2021-000843-33-GRHellenic Institute for the Study of Sepsis200
已完成
2 期
FEnofibRate as a Metabolic INtervention for COVID-19Covid19NCT04517396University of Pennsylvania701
已完成
3 期
A clinical trial to study the effect of fenofibrate or placebo supplementation along with antiepileptic therapy in persons with epilepsyCTRI/2021/03/032317Department of Pharmacology80
已完成
3 期
Fenofibrate in PSCIRCT20200427047225N1Shahid Beheshti University of Medical Sciences30
已完成
4 期
A CLINICAL TRIAL ON EFFECT OF SINGLE DOSE FENOFIBRATE AS AN ADJUNCT TO PHOTOTHERAPY IN NEONATAL JAUNDICECTRI/2023/03/050811Deepaa S94
