Chronic Liver DiseaseBCAA-CLDNCT04246918
Effect of BCAA Supplementation on Muscle Mass, Muscle Quality and Molecular Markers of Muscle Regeneration in CLD Patients
A study testing Branched Chain Amino Acid and Whey Protein concentrate powder in people with Chronic Liver Disease, run by Institute of Liver and Biliary Sciences, India at 1 site in India.
Trial summary
Loss of muscle mass (sarcopenia) is a major complication in a patient with cirrhosis, impacting the disease outcome, quality of life and survival. Cirrhotics lose muscle mass (MM) while waiting for liver transplant (LT) and even after LT, impacting the outcome of LT. Read more about this study
- Who is it for?
- Ages 18 to 60 years
- Conditions the study is for
- Chronic Liver Disease
- What is being tested?
- Branched Chain Amino Acid and Whey Protein concentrate powder
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 60 participants
- Where
- 1 siteIndia
- Study dates
- 1 Jun 2020to 30 Sep 2022
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 60 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- Patients with decompensated cirrhosis (CTP 7-9)
- Adult patients Age 18-60 years
- Patients with corrected BMI in the range <22.9
- Those who give consent for muscle biopsy
- INR <1.5 or 1.5-2.5 after correction with Vitamin K
- Platelets > 80000
- All etiologies
Who cannot join
- Presence of overt hepatic encephalopathy
- Patients with co-morbidities e.g. acquired immunodeficiency syndrome, HCC, Other cancer, Diabetes Mellitus, chronic kidney disease, congestive heart disease , chronic respiratory disease
- Patients with alcohol intake in past 3 months
- Patients with TIPS
- Patients on steroids
- INR >2.5
- Refusal to participate in the trial
Trial locations and contacts
1 site in 1 country.
India1 site
Institute of Liver and Biliary Sciences
New Delhi, National Capital Territory of Delhi, 110070
About this study
Official title: Effect of Branched Chain Amino Acids Supplementation on Muscle Mass, Muscle Quality and Molecular Markers of Muscle Regeneration in Patients With Chronic Liver Disease - A Randomized Controlled Trial.
Loss of muscle mass (sarcopenia) is a major complication in a patient with cirrhosis, impacting the disease outcome, quality of life and survival. Cirrhotics lose muscle mass (MM) while waiting for liver transplant (LT) and even after LT, impacting the outcome of LT. Moreover, LT is elusive for majority of patients in India. The pathophysiology of muscle loss is complicated, multifactorial, interlinked and primarily nutrition driven, which gives clues for targeted therapeutic modalities other than feeding alone. Experimental studies have instilled faith in BCAA in successfully counteracting the pathogenesis of muscle loss. But there is lack of convincing data from clinical studies with direct evidence on muscle growth per se.
Read the detailed description
Reduction in muscle mass (sarcopenia) is well documented in patients with chronic liver disease (CLD)leading to increased morbidity, mortality and poor quality of life. An equilibrium is maintained between the synthesis and degradation of muscles to maintain the muscle mass. However, an imbalance between the synthesis and degradation leads to loss of muscle mass. Various factors like alteration in dietary intake, hyper-metabolism, changes in amino acid profile, decreased physical activity, endotoxemia, hyperammonemia, increased myostatin levels have been postulated in the pathogenesis of muscle loss in liver disease. Reduced dietary intake, altered amino acid profile, decreased physical activity down regulate the anabolic pathway while the others increase the catabolic pathway. Increased level of myostatin inhibits the mTOR signaling and increases catabolism. Various therapeutic strategies such as increased calorie and protein intake, branched chain amino acid (BCAA) supplementation, late evening snack (LES), increased physical activity are the well accepted therapies. Hormone therapy (testosterone/growth hormone) also has been tried to improve muscle mass and function, reduce muscle catabolism in patients with CLD, however these newer treatment modalities i.e. hormone replacement, immune-nutrition and anti-myostatin antibodies are not free from adverse side-effects. Branched chain amino acids, a group of three essential amino acids (leucine, isoleucine, valine) have been tried since years in the setting of chronic liver disease patients for the treatment of hepatic encephalopathy and improvement in nutritional status. However, the studies assessing the impact of nutrition and BCAA in CLD have not assessed the direct impact on the muscle per se. The nutritional status has been assessed using different subjective methods like mid arm muscle circumference, triceps skin fold, nitrogen balance. Nutritional management is the cornerstone of the overall management of patients with cirrhosis, wherein BCAA constitutes an important therapeutic modality in the realm of nutrition in liver disease.
In the present study all the eligible cirrhotic patients will be randomized to a control group (receiving the nutritional therapy as per the standard nutritional practices and guidelines) or the intervention group (receiving BCAA supplementation over and above the standard nutrition therapy as per the standard nutritional practices and guidelines). Branched chain amino acids (BCAA) have the potential to up-regulate the anabolic pathway of muscle synthesis leading to improvement in muscle mass. Muscle mass as assessed by DEXA, along with changes in muscle histology, markers of the pathways that regulate muscle growth, functional capacity, and quality of life will be assessed after 3 months of BCAA intervention.
- Conditions
- Chronic Liver Disease
- Being tested
- Branched Chain Amino Acid, Whey Protein concentrate powder
- Keywords
- Chronic Liver Disease, Sarcopenia, Myostatin, Health related quality of life, muscle histology
- Medical subject headings
- Sarcopenia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Branched Chain Amino AcidDietary supplement
Branched chain amino acid is a group of three amino acids known for there role in muscle growth.
Whey Protein concentrate powderDietary supplement
Whey protein will be given to the standard treatment arm including in the same amount of 1.5gm/kg/IBW.
| Study group | Role | What they receive |
|---|---|---|
| Standard Treatment Group | Placebo comparator | The patients would receive customized diet charts providing 30-35Kcal/ideal body wt/day and 1.5 gm protein/ideal body wt/day) describing the food items along with the quantity and approximate household measurements. Diet would be so planned for each patient keeping in mind the individual food habits and choices. This group would not receive any supplement other than the prescribed diet. Whey protein will be included in this group. Receives: Dietary Supplement: Whey Protein concentrate powder |
| Intervention Arm | Active comparator | The patients would receive customized diet charts providing 30-35Kcal/ideal body wt/day and 1.5 gm protein/ideal body wt/day) describing the food items along with the quantity and approximate household measurements. Diet would be so planned for each patient keeping in mind the individual food habits and choices. In addition to the normal diet this group would receive 16gm of branched chain amino acid (BCAA) supplement (Commercial oral BCAA granules) daily in 4 divided doses, keeping the protein levels within the same range of 1.5 gm/Kg/day. Receives: Dietary Supplement: Branched Chain Amino Acid |
What is being measured
The primary outcome is the main question the study is designed to answer.
Improvement in the muscle mass
Muscle mass change as assessed by DEXA scan will be done.
Measured: 3 months
Secondary outcomes (19)
Changes in the muscle fibre type composition
Muscle fibre type will be assessed in muscle biopsy sample
Measured: 3 months
Changes in cross sectional area of muscle
Muscle fibre cross sectional area will be assessed in muscle biopsy sample
Measured: 3 months
Assessment of necrosis in muscle fibre
Muscle fibre necrosis will be assessed in muscle biopsy sample
Measured: 3 Months
Assessment of intramuscular fat deposition
Change in intramuscular fat deposition will be assessed in muscle biopsy sample.
Measured: 3 months
Assessment of myoD
Change in myoD will be assessed as marker of muscle regeneration in muscle biopsy sample
Measured: 3 month
Assessment of myogenin
Change in myogenin will be assessed as marker of muscle regeneration in muscle biopsy sample
Measured: 3 months
Assessment of PCNA
Change in PCNA as marker of satellite function will be assessed in muscle biopsy sample
Measured: 3 months
Assessment of proteosome C3, C5, C9
Change in these proteosome will be assessed in muscle biopsy sample
Measured: 3 months
Assessment of ubiquitin ligase E3
Change in Ubiquitin ligase E3 will be assessed in muscle biopsy sample.
Measured: 3 months
Assessment of myostatin level
Change in myostatin level will be assessed in blood sample using commercially available kit.
Measured: 3 months
Assessment of ammonia level
Change in ammonia level will be assessed in blood sample using commercially available kit
Measured: 3 months
Assessment of Insulin resistance
Insulin resistance will be calculated using homeostasis model for insulin resistance.
Measured: 3 Month
Assessment of IGF 1
IGF1 will be assessed using commercially available kit.
Measured: 3 Month
Assessment of Nutritional Status
Change Nutritional status will be assessed using bioelectrical impedance analysis
Measured: 3 Month
Assessment of Nitrogen balance
Change in nitrogen balance will be assessed using formula : Nitrogen Balance = Protein intake (gm) / 6.25 - (UUN + 4 gm)
Measured: 3 Month
Assessment of functional capacity
The Functional capacity of the patients would be assessed by Hand Grip Strength using the Handgrip Dynamometer .
Measured: 3 Months
Assessment of Clinical parameter- CTP
Clinical improvement will be assessed in terms of change in CTP score.
Measured: 3 Months
Assessment of Clinical parameter-MELD
Clinical improvement will be assessed in terms of change in MELD score.
Measured: 3 Months
Assessment of Health Related Quality of Life
The Health Related Quality of Life (HRQoL) of the patients would be assessed using the Chronic liver disease questionnaire(CLDQ)
Measured: 3 Months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 Jan 2020
- Study start1 Jun 2020
- Primary completion30 Sep 2022
- Study completion30 Sep 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Liver DiseaseStudies of the same condition, open and under way.
- More trials run by Institute of Liver and Biliary Sciences, IndiaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Open Label
- Masking
- None (open label)
- Enrolment
- 60 participants (actual)
Sponsor and investigators
- Lead sponsor
- Institute of Liver and Biliary Sciences, India
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Puja Bhatia, MSc, Principal investigator, Institute of Liver and Biliary Sciences, IndiaJaya Benjamin, PhD, Study director, Institute of Liver and Biliary Sciences, India
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04246918
- Sponsor's protocol ID
- ILBS-BCAA-02
- Acronym
- BCAA-CLD
- Status last verified
- Mar 2022
- First submitted
- 20 Jan 2020
- Last updated
- 31 Jan 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 31 Jan 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effect of Branched Chain Amino Acids Supplementation on Muscle Mass, Muscle Quality and Molecular Markers of Muscle Regeneration in Patients With Chronic Liver Disease - A Randomized Controlled Trial.
- ClinicalTrials.gov ID
- NCT04246918
- Acronym / sponsor ID
- BCAA-CLD / ILBS-BCAA-02
- Conditions
- Chronic Liver Disease
- Keywords
- Chronic Liver Disease, Sarcopenia, Myostatin, Health related quality of life, muscle histology
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- Institute of Liver and Biliary Sciences, IndiaUniversity, hospital or other
- Study start
- 1 Jun 2020 (actual)
- Primary completion
- 30 Sep 2022 (actual)
- Study completion
- 30 Sep 2022 (actual)
- First posted
- 29 Jan 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Loss of muscle mass (sarcopenia) is a major complication in a patient with cirrhosis, impacting the disease outcome, quality of life and survival. Cirrhotics lose muscle mass (MM) while waiting for liver transplant (LT) and even after LT, impacting the outcome of LT. Moreover, LT is elusive for majority of patients in India. The pathophysiology of muscle loss is complicated, multifactorial, interlinked and primarily nutrition driven, which gives clues for targeted therapeutic modalities other than feeding alone. Experimental studies have instilled faith in BCAA in successfully counteracting the pathogenesis of muscle loss. But there is lack of convincing data from clinical studies with direct evidence on muscle growth per se.
Detailed description
Reduction in muscle mass (sarcopenia) is well documented in patients with chronic liver disease (CLD)leading to increased morbidity, mortality and poor quality of life. An equilibrium is maintained between the synthesis and degradation of muscles to maintain the muscle mass. However, an imbalance between the synthesis and degradation leads to loss of muscle mass. Various factors like alteration in dietary intake, hyper-metabolism, changes in amino acid profile, decreased physical activity, endotoxemia, hyperammonemia, increased myostatin levels have been postulated in the pathogenesis of muscle loss in liver disease. Reduced dietary intake, altered amino acid profile, decreased physical activity down regulate the anabolic pathway while the others increase the catabolic pathway. Increased level of myostatin inhibits the mTOR signaling and increases catabolism. Various therapeutic strategies such as increased calorie and protein intake, branched chain amino acid (BCAA) supplementation, late evening snack (LES), increased physical activity are the well accepted therapies. Hormone therapy (testosterone/growth hormone) also has been tried to improve muscle mass and function, reduce muscle catabolism in patients with CLD, however these newer treatment modalities i.e. hormone replacement, immune-nutrition and anti-myostatin antibodies are not free from adverse side-effects. Branched chain amino acids, a group of three essential amino acids (leucine, isoleucine, valine) have been tried since years in the setting of chronic liver disease patients for the treatment of hepatic encephalopathy and improvement in nutritional status. However, the studies assessing the impact of nutrition and BCAA in CLD have not assessed the direct impact on the muscle per se. The nutritional status has been assessed using different subjective methods like mid arm muscle circumference, triceps skin fold, nitrogen balance. Nutritional management is the cornerstone of the overall management of patients with cirrhosis, wherein BCAA constitutes an important therapeutic modality in the realm of nutrition in liver disease.
In the present study all the eligible cirrhotic patients will be randomized to a control group (receiving the nutritional therapy as per the standard nutritional practices and guidelines) or the intervention group (receiving BCAA supplementation over and above the standard nutrition therapy as per the standard nutritional practices and guidelines). Branched chain amino acids (BCAA) have the potential to up-regulate the anabolic pathway of muscle synthesis leading to improvement in muscle mass. Muscle mass as assessed by DEXA, along with changes in muscle histology, markers of the pathways that regulate muscle growth, functional capacity, and quality of life will be assessed after 3 months of BCAA intervention.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Open Label
| Arm | Type | Receives |
|---|---|---|
| Standard Treatment Group | Placebo comparator | Dietary Supplement: Whey Protein concentrate powderThe patients would receive customized diet charts providing 30-35Kcal/ideal body wt/day and 1.5 gm protein/ideal body wt/day) describing the food items along with the quantity and approximate household measurements. Diet would be so planned for each patient keeping in mind the individual food habits and choices. This group would not receive any supplement other than the prescribed diet. Whey protein will be included in this group. |
| Intervention Arm | Active comparator | Dietary Supplement: Branched Chain Amino AcidThe patients would receive customized diet charts providing 30-35Kcal/ideal body wt/day and 1.5 gm protein/ideal body wt/day) describing the food items along with the quantity and approximate household measurements. Diet would be so planned for each patient keeping in mind the individual food habits and choices. In addition to the normal diet this group would receive 16gm of branched chain amino acid (BCAA) supplement (Commercial oral BCAA granules) daily in 4 divided doses, keeping the protein levels within the same range of 1.5 gm/Kg/day. |
Who may qualify
- Ages
- 18 to 60 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (7 listed)
- Patients with decompensated cirrhosis (CTP 7-9)
- Adult patients Age 18-60 years
- Patients with corrected BMI in the range <22.9
- Those who give consent for muscle biopsy
- INR <1.5 or 1.5-2.5 after correction with Vitamin K
Key exclusion criteria (7 listed)
- Presence of overt hepatic encephalopathy
- Patients with co-morbidities e.g. acquired immunodeficiency syndrome, HCC, Other cancer, Diabetes Mellitus, chronic kidney disease, congestive heart disease , chronic respiratory disease
- Patients with alcohol intake in past 3 months
- Patients with TIPS
- Patients on steroids
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Branched Chain Amino AcidBranched chain amino acid is a group of three amino acids known for there role in muscle growth. | Dietary supplement | Intervention Arm |
| Whey Protein concentrate powderWhey protein will be given to the standard treatment arm including in the same amount of 1.5gm/kg/IBW. | Dietary supplement | Standard Treatment Group |
Primary outcome
Improvement in the muscle mass
Time frame: 3 months
Muscle mass change as assessed by DEXA scan will be done.
19 secondary outcomes
Changes in the muscle fibre type composition
Time frame: 3 months
Changes in cross sectional area of muscle
Time frame: 3 months
Assessment of necrosis in muscle fibre
Time frame: 3 Months
Assessment of intramuscular fat deposition
Time frame: 3 months
Assessment of myoD
Time frame: 3 month
Assessment of myogenin
Time frame: 3 months
Assessment of PCNA
Time frame: 3 months
Assessment of proteosome C3, C5, C9
Time frame: 3 months
Assessment of ubiquitin ligase E3
Time frame: 3 months
Assessment of myostatin level
Time frame: 3 months
Assessment of ammonia level
Time frame: 3 months
Assessment of Insulin resistance
Time frame: 3 Month
Assessment of IGF 1
Time frame: 3 Month
Assessment of Nutritional Status
Time frame: 3 Month
Assessment of Nitrogen balance
Time frame: 3 Month
Assessment of functional capacity
Time frame: 3 Months
Assessment of Clinical parameter- CTP
Time frame: 3 Months
Assessment of Clinical parameter-MELD
Time frame: 3 Months
Assessment of Health Related Quality of Life
Time frame: 3 Months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Jan 2023.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Puja Bhatia, MSc principal investigator
Institute of Liver and Biliary Sciences, India
Jaya Benjamin, PhD study director
Institute of Liver and Biliary Sciences, India
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Branched Chain Amino Acid and Whey Protein concentrate powder in people with Chronic Liver Disease, run by Institute of Liver and Biliary Sciences, India at 1 site in India.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 31 Jan 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in India. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Improvement in the muscle mass (time frame: 3 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Jan 2023.