simvastatin
DrugSimvastatin 20 mg/day for 12 months
NCT Number: NCT03780673
The aim of this study is to assess the efficacy of oral administration of simvastatin plus rifaximin in patients with decompensated cirrhosis to halt the progression of the disease as assessed by prevention of the development of ACLF
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Phase 2 / Phase 3
University Hospitals Leuven, Leuven, Belgium
The current study was aimed at assessing whether a treatment based on combination of rifaximin and simvastatin would be effective in patients with decompensated cirrhosis to prevent ACLF development Considering that statins have been scarcely investigated in patients with decompensated cirrhosis due to a concern of potential higher liver and muscle toxicity in this population, a first LIVERHOPE_SAFETY clinical trial (unpublished) was undergone to assess safety and toxicity of statins with decompensated cirrhosis.
As a preliminary result of the LIVERHOPE_SAFETY clinical trial, it was concluded that the dose of Simvastatin 20mg per day plus Rifaximin is not associated to a higher risk of liver or muscle toxicity in patients with decompensated cirrhosis and simvastatin 20 mg was established for the LIVERHOPE_EFFICACY study.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Simvastatin 20 mg/day for 12 months
Rifaximin 400/8 hours for 12 months
Placebo of Simvastatin once a day for 12 months
Placebo of Rifaximin/8 hours for 12 months
Time frame: Month 12
Time frame: months 1, 3, 6, 9 and 12
Time frame: months 1, 3, 6, 9 and 12
Time frame: baseline and months 1, 3, 6, 9 and 12
Time frame: baseline and months 1, 3, 6, 9 and 12
Time frame: baseline and months 1, 3, 6, 9 and 12
Worsening of ascitis will be defined as increased diuretic dosage or need for large-volume parecentesis in patients who had never been treated with this procedure
Time frame: baseline and months 1, 3, 6, 9 and 12
Renal function impairment will be defined by AKI criteria, following criteria of the "EASL Clinical Practice Guidelines for the management of patients with decompensated cirrosis"
Time frame: baseline and months 1, 3, 6, 9 and 12
Time frame: baseline and months 1, 3, 6, 9 and 12
Time frame: baseline and months 1, 3, 6, 9 and 12
Time frame: baseline and months 1, 3, 6, 9 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: months 3, 6 and 12
Time frame: baseline and months 3, 6 and 12
The aim of this secondary endpoint is to identify phylogenetic and functional composition in the gut microbiota of patients at different stages of liver disease by analysis of microbial genes and signature.
As treatment with rifaximin has been associated to changes in microbiota composition in patients with cirrhosis, we will analyze the changes in microbiota signature and composition in patients under treatment with simvastatin and rifaximin at 3 months, 6 months and 12 months
Time frame: months 1, 3, 6, 9 and 12
MELD score is a system developed to evaluate the severity of chronic liver disease, and it involves serum bilirubin, creatinine and international normalized ratio values
Time frame: months 1, 3, 6, 9 and 12
CLIF-AD score is a system created to evaluate the prognosis of patients with decompensated cirrosis, and it involves age, white cell count, creatinine, international normalized ratio and sodium
Time frame: months 1, 3, 6, 9 and 12
Child Pugh is a score created to evaluate the prognosis of patients with cirrosis based on clinical and analytical values. It involves serum bilirubin, coagulation, albumin and the presence of clinical complications of cirrhosis, as hepatic encephalopathy and ascites
Time frame: baseline and months 1, 3, 6, 9 and 12
Evaluated by patient administration. CLDQ questionnaire contains 29 items divided into six domains: "Fatigue" which includes perceptions of decreased energy and sleepiness; "Emotional Function" which measures mood and insomnia; "Worry" assessing concerns regarding disease progression and family; "Activity" considering eating habits and movement of heavy objects; and finally, 2 symptom domains, "Abdominal Symptoms" and "Systemic Symptoms". All items refer to the previous 2 weeks on a 7 point Likert scale, with 1 corresponding to the maximum frequency ("all of the time") and 7 to the minimum ("none of the time"). Scores range from 1 (worst) to 7 (least severe), in which higher scores indicate a minimum frequency of symptoms and, consequently, a better quality of life
Time frame: baseline and months 1, 3, 6, 9 and 12
Liver Frailty Index questionnaire is an objectively measure "physical frailty" (a term that we believe embodies these extrahepatic manifestations of cirrhosis) in patients with end-stage liver disease (ESLD) and quantify its impact on health-related outcomes. It's composed by (1) Gender (Male or Female); (2) Dominant hand grip strength (kg), the means of three measures; (3) Chair stands (sec), time that it takes a patient to stand up and sit down in a chair 5 times without using their arms; and (4) Balance (sec), seconds holding 3 position balance tested in 3 positions for 10 seconds each the positions are side by side, semi tandem and tandem.
Liver Frailty Index is calculated as: (-0:330 * gender-adjusted grip strength) + (-2:529 * number of chair stands per second) + (-0:040 * balance time) + 6.
The questionnaire does not have a minimum value and a maximum value.
Time frame: baseline and months 1, 3, 6, 9 and 12
The PHES is a questionnaire used in the diagnosis of minimal hepatic encephalopathy (MHE) and can be used to assess motor speed, motor accuracy, concentration, attention, visual perception, visual-spatial orientation, visual construction and memory, which are related to most of neuropsychological impairments in MHE. The PHES is composed of five tests, number connection test-A (NCT-A), number connection test-B (NCT-B), serial dotting test (SDT), line tracing test (LTT) and digit symbol test (DST). This questionnaire measures the time that the patient spends doing the five exercises.
The questionnaire does not have a minimum value and a maximum value, but as the score increases there is a worsening of outcome.
Time frame: months 3, 6 and 9
Evaluated by patient administration. This questionnaire quantifies the presence of stigma among patients with cirrhosis. The questionnaire gives a total of 19 stigma-related questions with answer choices based on a four point Likert scale (strongly agree, agree, disagree, and strongly disagree). The questions are divided in four categories 1) discrimination, 2) stereotypes, 3) social isolation and 4) shame. The questionnaire does not have a minimum value and a maximum value, because is only a descriptive questionnaire that values patient perception regarding the disease.
Time frame: baseline and months 1, 3, 6, 9 and 12
Appearance of muscle toxicity at baseline, 1 month, 3 months, 6 months, 9 months and 12 months as defined using a specific statin-associated myopathy questionnaire. This questionnaire consists of four questions that patients can answer yes or no. The patients met the study definition for "appearance of muscle toxicity" if one of the three of the following occurred: 1) They reported new or increased muscle pain, cramps, or aching, unassociated with exercise; 2) Symptoms persisted for at least 2 weeks; 3) Symptoms resolved within 2 weeks of stopping the study drug; and 4) Symptoms reoccurred within 4 weeks of restarting the study medication.
Time frame: month 12
Time frame: months 1, 3, 6, 9 and 12
Time frame: months 1, 3, 6, 9 and 12
Time frame: months 1, 3, 6, 9 and 12
Time frame: month 12
Time frame: month 12
Time frame: month 12
Time frame: month 12
Judit Pich
Other
Efficacy of the Combination of Simvastatin Plus Rifaximin in Patients With Decompensated Cirrhosis to Prevent ACLF Development: a Multicenter, Double-blind, Placebo Controlled Randomized Clinical Trial
Acronym: 2018-001698-25
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04288323
Adenocarcinoma, Carcinoma
La Jolla, California, United States
View Trial DetailsNCT03620474
Blood-Borne Infections, Communicable Diseases
Ichikawa, Chiba, Japan
View Trial DetailsNCT03871894
Liver Cirrhoses
New Delhi, National Capital Territory of Delhi, India
View Trial DetailsNCT02367092
Atrophy, Digestive System Diseases
San Francisco, California, United States
View Trial Details