Testosterone Replacement in Non-alcoholic Steatohepatitis (TEREPINS) (TEREPINS)
Primary Purpose
Nonalcoholic Steatohepatitis, Hypogonadism
Status
Completed
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
testosterone undecanoate
Sponsored by
About this trial
This is an interventional treatment trial for Nonalcoholic Steatohepatitis focused on measuring nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, hypogonadism, testosterone replacement therapy
Eligibility Criteria
Inclusion Criteria:
- Abnormal serum ALT on >2 occasions over at least 3 months, despite standard lifestyle advice when appropriate, in regard to moderation of alcohol intake, weight reduction and exercise.
- Negative serological tests for hepatitis Bs ag and C antibody.
- Alcohol consumption >21 units per week for no more than 2 week in the last year and for no more than 3 months of the past 5 years, assessed using a lifetime alcohol consumption questionnaire.
- Liver biopsy, performed as part of clinical management within 6 months of recruitment, which shows all of: (a) steatosis (Kleiner grade 2 or 3); (b) NASH (combined intralobular inflammation and hepatocyte ballooning score of >1); (c) fibrosis Ishak stage <4; and (d) no evidence to suggest another major liver disease.
- Hypotestosteronaemia, defined by total serum testosterone <11 nmol/L . Investigators predict that this will include about 25% of men with NAFLD as defined above.
Exclusion Criteria:
- Inability to give informed consent.
- Age <18 or >75 years.
- Symptomatic sexual dysfunction.
- Cirrhosis either on baseline liver biopsy (Ishak score 5-6) or suggested by presence of varices, by ultrasound (small shrunken liver, ascites, splenomegaly) or by liver decompensation (encephalopathy, abnormal serum direct bilirubin, albumin or prothrombin time).
- Space occupying lesion on ultrasound with any suspicion of malignancy.
- Evidence of other chronic liver diseases pace occupying lesion on ultrasound with any suspicion of malignancy.
- Prostatic nodule or mass on PR examination unless full urological examination rules our prostate cancer
- Serum PSA or alpha feta protein above the age-specific normal range
- Carcinoma of male breast
- Taking medications (amiodarone, anti-retrovirals, sodium alproate, corticosteroids, tamoxifen) the previous 3 months (known to improve steatosis).
- Diabetes or hyperlipidaemia, where therapy has been changed within the last 12 months or with suboptimal control anticipating the need for change in therapy during the study.
- Severe or complicated obesity, likely requiring bariatric surgery in next 2 years.
- LH/FSH levels, raising the possibility of primary pituitary disease.
- Subject trying to or hoping to conceive within next 18 months.
- Haematocrit of >0.54
- History of any of the following: Sleep apnoea, breast or prostate or liver cancer, congestive heart failure, chronic renal failure (serum creatinine >150), severe chronic obstructive airways disease, uncontrolled hypertension epilepsy depression or migraine.
- Severe co morbidity likely in the opinion of the investigators to reduce life expectancy to <10 years.
- Hypersensitivity to active agent or to any of the excipients.
- On long-term warfarin or heparin-based anticoagulant therapy. Treatment with antiplatelet agents will not be an exclusion criterion, however, these will be omitted at the time of liver biopsies, as per normal clinical practice.
Sites / Locations
- Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
testosterone undecanoate
Arm Description
Open label testosterone injection. Testosterone Undecanoate (1 g in 4 ml oily base) will be given as slow (2 minute) intramuscular injections (Nebido, manufactured by Bayer-Schering). These will be administered by the study investigator or designated research nurse at time zero (baseline visit 2) and after 6, 18, 30 and 42 weeks.
Outcomes
Primary Outcome Measures
steatosis histology
Proportion of patients in whom severity of steatohepatitis improves with testosterone replacement therapy, assessed by liver biopsy
Secondary Outcome Measures
Proportion of patients in whom liver inflammation improves
Proportion of patients in whom liver inflammation improves
Proportion of patients in whom liver ballooning improves
Proportion of patients in whom liver ballooning improves
Proportion of patients in whom liver fibrosis improves
Proportion of patients in whom liver fibrosis improves
Change in fat content of liver
Change in fat content of liver assessed by by MR spectroscopy and its correlation with steatosis on liver biopsy
Change in HOMA index
measure of insulin sensitivity
Change in serum liver enzymes
Adverse events
Adverse events recorded over 12 month period
Full Information
NCT ID
NCT01919294
First Posted
August 6, 2013
Last Updated
April 25, 2017
Sponsor
Sheffield Teaching Hospitals NHS Foundation Trust
Collaborators
Bayer
1. Study Identification
Unique Protocol Identification Number
NCT01919294
Brief Title
Testosterone Replacement in Non-alcoholic Steatohepatitis (TEREPINS)
Acronym
TEREPINS
Official Title
Pilot Open Study of Testosterone Replacement in Non-alcoholic Steatohepatitis
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
July 2013 (undefined)
Primary Completion Date
January 30, 2017 (Actual)
Study Completion Date
January 30, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sheffield Teaching Hospitals NHS Foundation Trust
Collaborators
Bayer
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The main research questions are: In hypogonadal men with non-alcoholic steatohepatitis (NASH), does Testosterone Replacement Therapy (TRT), given for 12 months
improve severity of steatosis on liver biopsy (Primary Question)?
improve severity of associated steatohepatitis on liver biopsy?
reduce liver fat content as assessed by proton Magnetic Resonance Spectroscopy (1H-MRS)?
The work proposed here is an open pilot study of 10 patients, the main aim of which is to assess the effect size of TRT in regard to these end points (regarding which there are no published data), thereby allowing power calculations for a more definitive phase II trial. Other aims would be assessing recruitment and consent rates, which would also inform the design of the larger study.
Detailed Description
20-35% of adults have non-alcoholic fatty liver disease (NAFLD), which often leads to liver inflammation and damage and sometimes to cirrhosis, liver failure and liver cancer; it is now a common indication for liver transplantation in the UK. No medical treatment has been shown to be effective in preventing its progression.
Some men with NAFLD have low serum levels of testosterone (male hormone). Often, levels are only slightly low and do not cause symptoms. However there are several reasons to think that these low levels may be aggravating the liver disease. NAFLD is thought to be caused by resistance of tissues to the actions of the hormone insulin (Insulin Resistance or IR). Low testosterone levels may cause IR. Treatments for prostatic cancer which lower testosterone levels result in both IR and in NAFLD. Mice who cannot produce testosterone also develop NAFLD and this is reversed by testosterone replacement.
The investigators therefore speculate that testosterone replacement in men with NAFLD and low blood testosterone levels will reduce liver fat. Investigators will study 10 men with NAFLD and some inflammation or scarring (proven on liver biopsy performed for clinical diagnosis) and who have mildly reduced testosterone levels. Investigators will see if giving a 12 month course of Testosterone Replacement Therapy (TRT) to these men will lessen the severity of their liver damage.
Consented patients will be seen after 6, 18, 30, 42 and 52 weeks. Patients will undergo a baseline clinical assessment, blood tests, an ultra sound scan, magnetic resonance scanning of the liver (to estimate liver fat), and a repeat liver biopsy to end the study.
Patients will complete questionnaires, and undergo clinical assessment, blood tests, an ultrasound scan, and magnetic resonance (MR) scanning of the liver (to estimate liver fat) at baseline. Patients will have clinical assessments and blood tests at 6-weekly intervals for 12 months. At 12 months patients will have a repeat liver biopsy, ultrasound and MR scan.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nonalcoholic Steatohepatitis, Hypogonadism
Keywords
nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, hypogonadism, testosterone replacement therapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
3 (Actual)
8. Arms, Groups, and Interventions
Arm Title
testosterone undecanoate
Arm Type
Experimental
Arm Description
Open label testosterone injection. Testosterone Undecanoate (1 g in 4 ml oily base) will be given as slow (2 minute) intramuscular injections (Nebido, manufactured by Bayer-Schering). These will be administered by the study investigator or designated research nurse at time zero (baseline visit 2) and after 6, 18, 30 and 42 weeks.
Intervention Type
Drug
Intervention Name(s)
testosterone undecanoate
Other Intervention Name(s)
Nebido
Intervention Description
Preparation: 1 gram in 4 ml of oily base. Requires no special storage conditions. Proposed regime: 1 mg as a single intramuscular injection at 0, 6, 18, 30 and 42 weeks
Primary Outcome Measure Information:
Title
steatosis histology
Description
Proportion of patients in whom severity of steatohepatitis improves with testosterone replacement therapy, assessed by liver biopsy
Time Frame
baseline and 12 months
Secondary Outcome Measure Information:
Title
Proportion of patients in whom liver inflammation improves
Description
Proportion of patients in whom liver inflammation improves
Time Frame
baseline and 12 months
Title
Proportion of patients in whom liver ballooning improves
Description
Proportion of patients in whom liver ballooning improves
Time Frame
baseline and 12 months
Title
Proportion of patients in whom liver fibrosis improves
Description
Proportion of patients in whom liver fibrosis improves
Time Frame
baseline and 12 months
Title
Change in fat content of liver
Description
Change in fat content of liver assessed by by MR spectroscopy and its correlation with steatosis on liver biopsy
Time Frame
baseline and 12 months
Title
Change in HOMA index
Description
measure of insulin sensitivity
Time Frame
baseline and 12 months
Title
Change in serum liver enzymes
Time Frame
baseline and 12 months
Title
Adverse events
Description
Adverse events recorded over 12 month period
Time Frame
12 months
Other Pre-specified Outcome Measures:
Title
Study recruitment rate
Description
With regard to this being a pilot feasibility study, the recruitment rate and level of data completeness achieved during the study will be assessed.
Time Frame
24 months
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Abnormal serum ALT on >2 occasions over at least 3 months, despite standard lifestyle advice when appropriate, in regard to moderation of alcohol intake, weight reduction and exercise.
Negative serological tests for hepatitis Bs ag and C antibody.
Alcohol consumption >21 units per week for no more than 2 week in the last year and for no more than 3 months of the past 5 years, assessed using a lifetime alcohol consumption questionnaire.
Liver biopsy, performed as part of clinical management within 6 months of recruitment, which shows all of: (a) steatosis (Kleiner grade 2 or 3); (b) NASH (combined intralobular inflammation and hepatocyte ballooning score of >1); (c) fibrosis Ishak stage <4; and (d) no evidence to suggest another major liver disease.
Hypotestosteronaemia, defined by total serum testosterone <11 nmol/L . Investigators predict that this will include about 25% of men with NAFLD as defined above.
Exclusion Criteria:
Inability to give informed consent.
Age <18 or >75 years.
Symptomatic sexual dysfunction.
Cirrhosis either on baseline liver biopsy (Ishak score 5-6) or suggested by presence of varices, by ultrasound (small shrunken liver, ascites, splenomegaly) or by liver decompensation (encephalopathy, abnormal serum direct bilirubin, albumin or prothrombin time).
Space occupying lesion on ultrasound with any suspicion of malignancy.
Evidence of other chronic liver diseases pace occupying lesion on ultrasound with any suspicion of malignancy.
Prostatic nodule or mass on PR examination unless full urological examination rules our prostate cancer
Serum PSA or alpha feta protein above the age-specific normal range
Carcinoma of male breast
Taking medications (amiodarone, anti-retrovirals, sodium alproate, corticosteroids, tamoxifen) the previous 3 months (known to improve steatosis).
Diabetes or hyperlipidaemia, where therapy has been changed within the last 12 months or with suboptimal control anticipating the need for change in therapy during the study.
Severe or complicated obesity, likely requiring bariatric surgery in next 2 years.
LH/FSH levels, raising the possibility of primary pituitary disease.
Subject trying to or hoping to conceive within next 18 months.
Haematocrit of >0.54
History of any of the following: Sleep apnoea, breast or prostate or liver cancer, congestive heart failure, chronic renal failure (serum creatinine >150), severe chronic obstructive airways disease, uncontrolled hypertension epilepsy depression or migraine.
Severe co morbidity likely in the opinion of the investigators to reduce life expectancy to <10 years.
Hypersensitivity to active agent or to any of the excipients.
On long-term warfarin or heparin-based anticoagulant therapy. Treatment with antiplatelet agents will not be an exclusion criterion, however, these will be omitted at the time of liver biopsies, as per normal clinical practice.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dermot Gleeson, MD
Organizational Affiliation
Sheffield Teaching Hospitals NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust
City
Sheffield
State/Province
South Yorkshire
ZIP/Postal Code
S10 2JF
Country
United Kingdom
12. IPD Sharing Statement
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Testosterone Replacement in Non-alcoholic Steatohepatitis (TEREPINS)
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