Vitamin B-6 and Glutathione on Inflammation, Homocysteine, Oxidative Stress and Antioxidant Capacities
Primary Purpose
Liver Cirrhosis, Liver Cancer
Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
vitamin B-6
Glutathione
Dextrins
Sponsored by
About this trial
This is an interventional prevention trial for Liver Cirrhosis
Eligibility Criteria
Inclusion Criteria:
- age between 20 to 80 years old
- patients are diagnosed as cirrhosis or cirrhosis combined with hepatocellular carcimoma
Exclusion Criteria:
- patients are currently taking any nutrient supplements
- patients with cardiac, renal, gastrointestinal or diabetic diseases
- patients are currently taking any medication which will interfere with vitamin B-6 or glutathione metabolism〔i.e., phenobarbital, phenytoin, cycloserine, pyrazinamide, isoniazid, (thio)semicarbazide, hydramitrazine, phenelzine, carbidopa, levodopa, hydralazine, steroids and penicillamine)
- patients are in pregnant or lactation.
Sites / Locations
- Taichung Veterans General HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Placebo Comparator
Experimental
Experimental
Experimental
Arm Label
Negative control
Supplement 1
Supplement 2
Supplement 3
Arm Description
Dextrins
50 mg/d vitamin B-6
500 mg/d Glutathione
50 mg/d vitamin B-6 plus 500 mg/d Glutathione
Outcomes
Primary Outcome Measures
Oxidative stress marker (MDA concentation)
Secondary Outcome Measures
Glutathione related enzyme activities
Full Information
NCT ID
NCT02321579
First Posted
December 9, 2014
Last Updated
December 19, 2014
Sponsor
Taichung Veterans General Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02321579
Brief Title
Vitamin B-6 and Glutathione on Inflammation, Homocysteine, Oxidative Stress and Antioxidant Capacities
Official Title
The Effects of Vitamin B-6 and Glutathione on Inflammatory Responses, Homocysteine Metabolism, Oxidative Stress and Antioxidant Capacities in Patients With Liver Cirrhosis or Hepatocellular Carcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
December 2014
Overall Recruitment Status
Unknown status
Study Start Date
December 2014 (undefined)
Primary Completion Date
December 2016 (Anticipated)
Study Completion Date
July 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Taichung Veterans General Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study is designed as a hospital-based cross-sectional and randomized placebo-controlled intervention trial. One hundred and fifty patients with either cirrhosis or cirrhosis combined with hepatocellular carcinoma (HCC) who meet the inclusion criteria will be recruited from Taichung General Veterans Hospital. One hundred patients will be randomly assigned to either the 1) placebo group (n = 25); 2) vitamin B-6 group; (50 mg/d, n = 25); 3) glutathione (GSH) group (500 mg/d, n = 25); or 4) vitamin B-6 (50 mg/d) plus GSH (500 mg/d) group (n = 25) for 3 mo. Data on demography, anthropometry and medical history will be collected. Patients with cirrhosis or cirrhosis combined with HCC will have fasting blood drawn in the clinics. Additionally, patients who participated in the intervention study will have blood drawn at month 0, 1, 2 and 3 during intervention period. Hematological measurements, plasma vitamin B-6 status, GSH, inflammatory markers, homocysteine, cysteine, SAM, SAH, oxidative stress indicator, oxidized GSH and GSH related antioxidant enzyme activities will be analyzed.
Detailed Description
Liver cirrhosis is now the ninth leading cause of death and hepatocellular carcinoma (HCC) is the second leading cause of cancer mortality among men and women in Taiwan. Vitamin B-6 and glutathione (GSH) are metabolized in liver, the role of vitamin B-6 and GSH playing in the inflammatory responses and antioxidant function would be impaired during hepatic injury. The purpose of this study is going to assess the effects of individual or combined supplementation of vitamin B-6 and GSH on homocysteine, cysteine, the ratio of S-adenosylmethionine (SAM)/S-adenosylhomocysteine (SAH), oxidative stress, oxidized glutathione (GSSG) and GSH related antioxidant enzyme activities in patients with cirrhosis and cirrhosis combined with HCC.
This study is designed as a hospital-based cross-sectional and randomized placebo-controlled intervention trial. One hundred and fifty patients with either cirrhosis or cirrhosis combined with HCC who meet the inclusion criteria will be recruited from Taichung General Veterans Hospital. One hundred patients will be randomly assigned to either the 1) placebo group (n = 25); 2) vitamin B-6 group; (50 mg/d, n = 25); 3) GSH group (500 mg/d, n = 25); or 4) vitamin B-6 (50 mg/d) plus GSH (500 mg/d) group (n = 25) for 3 mo. Data on demography, anthropometry and medical history will be collected. Patients with cirrhosis or cirrhosis combined with HCC will have fasting blood drawn in the clinics. Additionally, patients who participated in the intervention study will have blood drawn at month 0, 1, 2 and 3 during intervention period. Hematological, plasma vitamin B-6 status, GSH, inflammatory markers, homocysteine, cysteine, SAM, SAH, oxidative stress indicator, GSSG and GSH related antioxidant enzyme activities will be measured.
Hopefully, the results of this study could provide more pictures on the beneficial effects of vitamin B-6 and GSH supplementation on inflammatory responses, homocysteine, cysteine, the ratio of SAM/SAH, oxidative stress, GSSG and GSH related antioxidant enzyme activities in patients with cirrhosis and HCC.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Cirrhosis, Liver Cancer
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
25 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Negative control
Arm Type
Placebo Comparator
Arm Description
Dextrins
Arm Title
Supplement 1
Arm Type
Experimental
Arm Description
50 mg/d vitamin B-6
Arm Title
Supplement 2
Arm Type
Experimental
Arm Description
500 mg/d Glutathione
Arm Title
Supplement 3
Arm Type
Experimental
Arm Description
50 mg/d vitamin B-6 plus 500 mg/d Glutathione
Intervention Type
Dietary Supplement
Intervention Name(s)
vitamin B-6
Intervention Description
50 mg/d
Intervention Type
Dietary Supplement
Intervention Name(s)
Glutathione
Intervention Description
500 mg/d
Intervention Type
Dietary Supplement
Intervention Name(s)
Dextrins
Intervention Description
50 mg/d
Primary Outcome Measure Information:
Title
Oxidative stress marker (MDA concentation)
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Glutathione related enzyme activities
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age between 20 to 80 years old
patients are diagnosed as cirrhosis or cirrhosis combined with hepatocellular carcimoma
Exclusion Criteria:
patients are currently taking any nutrient supplements
patients with cardiac, renal, gastrointestinal or diabetic diseases
patients are currently taking any medication which will interfere with vitamin B-6 or glutathione metabolism〔i.e., phenobarbital, phenytoin, cycloserine, pyrazinamide, isoniazid, (thio)semicarbazide, hydramitrazine, phenelzine, carbidopa, levodopa, hydralazine, steroids and penicillamine)
patients are in pregnant or lactation.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yi-Chia Huang, PhD
Phone
+886-4-24730022
Ext
12198
Email
ych@csmu.edu.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shao-Bin Cheng, MD
Organizational Affiliation
Taichung Veterans General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Taichung Veterans General Hospital
City
Taichung
ZIP/Postal Code
40705
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yi-Chia Huang, PhD
Phone
+886-4-24730022
Ext
12198
Email
ych@csmu.edu.tw
First Name & Middle Initial & Last Name & Degree
Shao-Bin Cheng, MD
12. IPD Sharing Statement
Learn more about this trial
Vitamin B-6 and Glutathione on Inflammation, Homocysteine, Oxidative Stress and Antioxidant Capacities
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