The Efficacy and Safety of Pioglitazone in Patients With Nonalcoholic Steatohepatitis
Recruitment status was Recruiting
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Purpose
Recent studies have demonstrated that PPARγ as well as diet control could improve glycemic control, decrease serum ALT level, decrease hepatic fat distribution, and increase intrahepatic insulin sensitivity. The purposes of this study are:
1. Primary aims:
- Comparison between Pioglitazone and placebo groups in terms of steatosis and liver function tests.
- Evaluation of clinical safety of Pioglitazone
2. Secondary aims:
- Comparison between Pioglitazone and placebo groups in terms of liver necroinflammation and fibrosis.
- The impact of Pioglitazone on the related metabolic index, including insulin resistance(HOMA-IR), newly-onset diabetes, metabolic syndrome, lipid profiles (T-Chol, HDL-C, LDL-C, TG).
- Comparison between Pioglitazone and placebo groups in terms of high-sensitive C-reactive protein changes.
3. Interventional aim: Assessment the association between magnetic resonance imaging study and intrahepatic fat distribution before and after Pioglitazone treatment.
| Condition | Intervention | Phase |
|---|---|---|
|
Hepatitis |
Drug: Pioglitazone Drug: placebo |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator) Primary Purpose: Treatment |
| Official Title: | A Double-Blind, Randomized, Placebo-Controlled, Phase II Study to Assess the Efficacy and Safety of Pioglitazone in Patients With Nonalcoholic Steatohepatitis |
- Comparison between Pioglitazone and placebo groups in terms of steatosis and liver function tests [ Time Frame: 9 months ] [ Designated as safety issue: Yes ]
- Evaluation of clinical safety of Pioglitazone [ Time Frame: 9 months ] [ Designated as safety issue: Yes ]
- Comparison between Pioglitazone and placebo groups in terms of liver necroinflammation and fibrosis. [ Time Frame: 9 months ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 90 |
| Study Start Date: | April 2009 |
| Estimated Study Completion Date: | July 2012 |
| Estimated Primary Completion Date: | March 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Pioglitazone
Pioglitazone 30 mg/day for 6 months and 3 months of follow-up period after treatment
|
Drug: Pioglitazone
Other Name: GLITOS
|
|
Placebo Comparator: Placebo
Placebo 30 mg/day for 6 months and 3 months of follow-up period after treatment
|
Drug: placebo
placebo 30 mg/d for 6 months
|
Detailed Description:
Pioglitazone belongs to thiazolidinediones and anti-diabetes drug which decreases the insulin resistance. It increases the use of glucose of peripheral tissues and decrease the production of glucose from liver and dose not influence the production of insulin. It is agonist of peroxisome proliferator-activated receptor-gamma (PPARγ) and by binding to the receptors of PPARγ in various tissues it has effects on transcription of the insulin-dependent gene. In animal model, pioglitazone has shown to influence the metabolism by the insulin-dependent mechanism.
Recent studies have demonstrated that PPARγ as well as diet control could improve glycemic control, decrease serum ALT level, decrease hepatic fat distribution, and increase intrahepatic insulin sensitivity. Meanwhile, PPARγ could also prevent the development of alcohol-induced steatohepatitis, improve hepatic necroinflammatory activity, and decrease lipid deposition. It is not yet clearly known how the effect of P-PARγ agonist among Asian peoples.
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Main inclusion criteria:
- Male and female patients with 18-70 years of age
- Liver biopsy findings consistent with the diagnosis of NASH with or without compensated cirrhosis within one year before baseline
- Compensated liver disease
- Negative urine or blood pregnancy test (for women of childbearing potential) documented within the 24-hour period prior to the first dose of study drug
- All fertile males and females must be using two forms of effective contraception during treatment during the 3 months after treatment.
- ALT level between 1.3-5 x ULN for 2 occasions during 6 months before screening.
- HbA1C ≦ 8.0 during screening
Main exclusion criteria:
- Therapy with any systemic anti-neoplastic or immunomodulatory treatment (including supraphysiologic doses of steroids and radiation) *6 months before baseline.
- History or other evidence of a medical condition associated with chronic liver disease other than NASH (e.g., hemochromatosis, autoimmune hepatitis, alcoholic liver disease, > 20 g/day for female or > 40 g/day for male, toxin exposures)
- hepatocellular carcinoma
- History or other evidence of bleeding from esophageal varices or other conditions consistent with decompensated liver disease
- Serum creatinine level >1.5 times the upper limit of normal at screening and calculated creatinine clearance as calculated by Cockcroft and Gault < 60mL/min during screening
- History of ischemic heart disease during screening
- New York Heart Association (NYHA) Functional Class 1-4 cardiac status during screening
- Albumin <3.2g/dL during screening
- Total bilirubin >1.2 x ULN during screening. Patients with history of asymptomatic indirect hyperbilirubinemia whose total bilirubin < 2 x ULN and direct bilirubin < 20% of total bilirubin could be included.
- History of prothrombin time > 15 seconds or International normalized ratio (INR) > 1.3
- Organ, stem cell, or bone marrow transplant
- History of serious concurrent medical illness that in the investigator's opinion might interfere with therapy this includes significant systemic illnesses (other than liver disease) such as chronic pancreatitis
- Active systemic autoimmune disorder
- Pregnancy (or lactation) or, in subjects capable of bearing children, inability / unwillingness to practice adequate contraception
- Females of child-bearing potential (post-puberty) unwilling or unable to have pregnancy testing at any study visit
- Therapy with a systemic antiviral agent (with the exception of prophylaxis or treatment of influenza or chronic HSV) within the past 30 days prior to screening.
- Concurrent participation in another clinical trial in which the subject is or will be exposed to another investigational or a non-investigational drug or device within 6 weeks of the screening visit
- Current therapy with insulin within 1 week prior to screening.
- Experienced use with PPARg agonist (e.g., rosiglitazone, pioglitazone) within 6 months prior to screening.
- Known hypersensitivity to any component of PPARg agonists
- A history of hepatotoxicity to TZDs and/or a history of severe edema or a medically serious fluid-related event associated with the use of TZDs
- History of metformin use within 3 months prior to screening.
- Type Ⅰ diabetes
- Seropositive of HBsAg, anti-HCV or anti-HIV during screening or 3 month prior to screening.
Contacts and Locations| Contact: Wan-Long Chuang, MD, PhD | 886 7 3208282 | waloch@kmu.edu.tw; research.kmuhb@gmail.com |
| Taiwan | |
| Kaohsiung Medical University Hospital | Recruiting |
| Kaohsiung, Taiwan, 803 | |
| Contact: Wan-Long Chuang, MD, PhD 886 7 3208282 waloch@kmu.edu.tw; research.kmuhb@gmail.com | |
| Principal Investigator: Wan-Long Chuang, MD, PhD | |
| Kaohsiung Municipal Hsiao-Kang Hospital, Kaohsiung Medical University | Recruiting |
| Kaohsiung City, Taiwan, 812 | |
| Contact: Jee-Fu Huang, MD. 88678036783 ext 3440 jf71218@gmail.com | |
| Principal Investigator: Wan-Long Chuang, MD., PhD. | |
| Principal Investigator: | Wan-Long Chuang, MD, PhD | Kaohsiung Medical University |
More Information
No publications provided
| Responsible Party: | Kaohsiung Medical University Hospital |
| ClinicalTrials.gov Identifier: | NCT01068444 History of Changes |
| Other Study ID Numbers: | KMUH-HB9608 |
| Study First Received: | February 11, 2010 |
| Last Updated: | February 12, 2010 |
| Health Authority: | Taiwan: Department of Health |
Keywords provided by Kaohsiung Medical University Chung-Ho Memorial Hospital:
|
NASH Pioglitazone Treatment |
Additional relevant MeSH terms:
|
Hepatitis Hepatitis A Fatty Liver Liver Diseases Digestive System Diseases Hepatitis, Viral, Human Virus Diseases |
Enterovirus Infections Picornaviridae Infections RNA Virus Infections Pioglitazone Hypoglycemic Agents Physiological Effects of Drugs Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 19, 2013