Quality of Life and Nutritional Improvements in Cirrhotic Patients Following Hepatic Encephalopathy Using Rifaximin.
试验速览
- 阶段
- 4 期
- 状态
- 终止
- 入组人数
- 4
- 试验地点
- 1
- 主要终点
- Outcomes of Change in Quality of Life Assessment Between the Two Groups
研究概览
简要总结
The purpose of this study is to determine whether taking Rifaximin (Xifaxan) in conjunction with the use of nutritional concepts is effective in improving morbidity and quality of life in cirrhotic patients suffering from hepatic encephalopathy (HE).
详细描述
Prevention of portal hypertension complications should be at the forefront. In doing so, the end result will be an improvement in the multitude of morbidity and mortality issues. The proposed prospective trial will compare patients with similar demographics and medical and clinical settings utilizing standard of care therapy. Study subjects will be randomly assigned into two treatment groups. Group one will receive Lactulose 30ml three times a day as SOC and Rifaximin Placebo 550mg twice a day with nutritional supervision and group two will receive Rifaximin 550mg twice per day as SOC and Lactulose placebo 30ml three times per day with nutritional supervision.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Care Provider, Investigator)
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
- •Male and female gender of Age 18 years or older
- •Liver cirrhosis defined as one or more of the following: Radio-graphically proven portal hypertension (CT with nodular appearance) or Liver biopsy with cirrhosis
- •Model for End Stage Liver Disease (MELD) score < 20
- •Willingness to provide written informed consent, and participate in all study requirements
- •Sodium greater than 130 meq/L
- •Conn Score < 2
排除标准
- •Active alcohol consumption
- •Serum total bilirubin level > 5 mg/dl
- •History of hepatocellular carcinoma (HCC) and malignancies other than basal cell carcinoma of the skin
- •Pregnant or breastfeeding women
- •Subject has renal insufficiency requiring routine dialysis
- •Poorly controlled diabetes as defined by HgA1C > 10
- •Narcotic/psychotropic usage other than a stable dose of antidepressant and/or methadone. Neurontin (gabapentin) and Lyrica (pregabalin) are permitted if the subject has been on a stable dose for at least 2 months prior to the screening visit and no change of dosing is expected throughout the length of the trial
- •Any of the following diagnoses:
- •Evidence of severe concomitant illness or any condition that makes them unsuitable for the study in the opinion of the investigator(s)
- •Subject has received an investigational drug within 30 days prior to enrollment
研究组 & 干预措施
Lactulose and Rifaximin Placebo
Standard portal hypertension care, standard nutritional advice, Lactulose 30ml three times a day and Rifaximin (Xifaxan) Placebo twice a day.
干预措施: Lactulose (Drug)
Lactulose and Rifaximin Placebo
Standard portal hypertension care, standard nutritional advice, Lactulose 30ml three times a day and Rifaximin (Xifaxan) Placebo twice a day.
干预措施: Rifaximin Placebo (Drug)
Rifaximin and Lactulose Placebo
Rifaximin (Xifaxan) twice a day and Lactulose Placebo three times a day.
干预措施: Rifaximin (Drug)
Rifaximin and Lactulose Placebo
Rifaximin (Xifaxan) twice a day and Lactulose Placebo three times a day.
干预措施: Lactulose Placebo (Drug)
结局指标
主要结局
Outcomes of Change in Quality of Life Assessment Between the Two Groups
时间窗: Participants will be followed for 180 days
Quality of Life will be determined by the Chronic Liver Disease Foundation Questionnaire (CLDQ), the Sleep Scale by Hays, R.D.\&Stewart, A.L. and the Multidimensional Assessment of Fatigue (MAF) Scale and measured based upon Subjective Global Assessment (SGA).
Nutritional Improvement Between the Two Groups
时间窗: Participants will be followed for 180 days
These outcomes will be determined as Body Composition Analysis via the Quadscan 4000 BIA device manufactured by Bodystat;calories burned, steps taken and levels of physical activity to sleep efficiency will be measured via the Bodymedia CORE Fit actigraph device and various standard of care laboratories.
次要结局
- Markers of improvement in general health(Participants will be followed for 180 days)
研究者
Guy Neff, MD
Medical Doctor
Tampa General Hospital