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出境医 / 临床实验 / Efficacy and Safety of Testosterone Therapy in Improving Sarcopenia in Men With Cirrhosis.

Efficacy and Safety of Testosterone Therapy in Improving Sarcopenia in Men With Cirrhosis.

Study Description
Brief Summary:
  • Study Population- Patient with cirrhosis with any aetiology with sarcopenia visiting ILBS OPD/IPDs who are willing to visit ILBS gymnasium twice weekly for first month.
  • Study Design- A Prospective Randomized Controlled Trial
  • Study Period- Study will be conducted at ILBS from April 2019 to Oct 2019

    • Sample Size:As shown by Eva Roman et al - in cirhotics with sarcopenia exercise increases mean lean appendicular mass , by 0.38 kg (14 patients, p < 0.03), and Sinclair et al has shown testosterone (22 patients, p <0.05)) to increase mean Appendicular lean mass by +1.69 kg - for 10% increase in APLM
    • we need to enroll 40 patients in each arm, and considering a los to follow up approx.10% , will require minimum 44 patients in each arm
    • We will therefore enroll and randomize 100 patients with 50 in each arm.

Intervention - Testosterone Supplementation - Intramuscular Testosterone Undecanoate 1000 Mg (4 ml volume in oily base) will be injected into the upper, outer quadrant of the buttock at 0, 6, 12,16,20, 24 weeks according to manufacturer recommendations.

Monitoring and assessment - On every visit patient will be inquired or evaluated for side effects like local site pain or hematoma , hypertension, headache, allergic reactions, acne, nausea , mood swings, pedal edema , breast enlargement and others.


Condition or disease Intervention/treatment Phase
Liver Cirrhosis Drug: Testosterone Supplementation Drug: Standard Medical Treatment Other: Exercise Not Applicable

Study Design
Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 100 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Efficacy and Safety of Testosterone Therapy in Improving Sarcopenia in Men With Cirrhosis a Randomized Controlled Trial
Actual Study Start Date : July 4, 2019
Estimated Primary Completion Date : June 30, 2020
Estimated Study Completion Date : June 30, 2020
Arms and Interventions
Arm Intervention/treatment
Experimental: Standard Medical Treatment +Intramuscular Testosterone + Exerc
Intramuscular Testosterone Undecanoate 1000 Mg (4 ml volume in oily base) will be injected into the upper, outer quadrant of the buttock at 0, 6, 12,16,20, 24 weeks according to manufacturer recommendations
Drug: Testosterone Supplementation
Intramuscular Testosterone Undecanoate 1000 Mg (4 ml volume in oily base) will be injected into the upper, outer quadrant of the buttock at 0, 6, 12,16,20, 24 weeks according to manufacturer recommendations

Drug: Standard Medical Treatment
Standard Medical Treatment

Other: Exercise
Exercise

Active Comparator: Standard Medical Treatment+Exercise
Standard Medical Treatment +Exercise
Drug: Standard Medical Treatment
Standard Medical Treatment

Other: Exercise
Exercise

Outcome Measures
Primary Outcome Measures :
  1. Increase in Lean Appendicular Muscle Mass by more than 10% in both groups [ Time Frame: 24 weeks ]

Secondary Outcome Measures :
  1. Improvement by 10 % in Hand Grip strength in both groups [ Time Frame: 24 weeks ]
  2. Improvement by 10 % in6 minute walk distance in both groups [ Time Frame: 24 weeks ]
  3. Improvement by 10 % in the increased bone and muscle mass in both groups [ Time Frame: 24 weeks ]
  4. Improvement by 10 % L3 Skeletal Muscle Index in both groups. [ Time Frame: 24 weeks ]
  5. Improvement by 10 % in serum ammonia levels in both groups [ Time Frame: 24 weeks ]
  6. Improvement by 10 % in muscle fibres on Biopsy in both groups • [ Time Frame: 24 weeks ]
  7. Reduction in Myostatin level in both groups [ Time Frame: 24 weeks ]
  8. Improvement in MELD scores in both groups [ Time Frame: 24 weeks ]
  9. Decrease in mortality over 6 months in both groups [ Time Frame: 24 weeks ]
  10. Changes in HBA1C level in both groups [ Time Frame: 24 weeks ]
  11. Reduction in requirement of hospital admissions in both groups [ Time Frame: 24 weeks ]
  12. Decrease in TNF alpha levels in both groups [ Time Frame: 24 weeks ]

Eligibility Criteria
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Ages Eligible for Study:   18 Years to 55 Years   (Adult)
Sexes Eligible for Study:   All
Gender Based Eligibility:   Yes
Gender Eligibility Description:   Males only
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Men with cirrhosis of any etiology
  • Sarcopenia
  • CTP 6-12

Exclusion Criteria:

  • Hepatocellular carcinoma
  • Other known malignancy,
  • CTP > 12
  • Acute liver injury
  • Prostate disease,
  • Known hypersensitivity to testosterone therapy,
  • Polycythaemia (haematocrit >55%),
  • Uncontrolled hypertension (>160/90 mmHg despite treatment),
  • Uncontrolled obstructive sleep apnoea,
  • Severe renal dysfunction (estimated glomerular filtration rate <30ml/min)
  • Uncontrolled epilepsy, migraine, or significant cardiac insufficiency (New York Heart Association class III or IV or LVEF < 45-50%.
  • CKD (Chronic Kidney Disease) - eGFR (Glomerular Filtration Rate) <60%
  • Platelet count below 30,000 or taking warfarin
  • Failure to give consent.
Contacts and Locations

Contacts
Layout table for location contacts
Contact: Dr Shushrut Singh, MD 01146300000 drsushrut20@gmail.com

Locations
Layout table for location information
India
Institute of Liver & Biliary Sciences Recruiting
New Delhi, Delhi, India, 110070
Sponsors and Collaborators
Institute of Liver and Biliary Sciences, India
Tracking Information
First Submitted Date  ICMJE June 19, 2019
First Posted Date  ICMJE June 24, 2019
Last Update Posted Date August 21, 2019
Actual Study Start Date  ICMJE July 4, 2019
Estimated Primary Completion Date June 30, 2020   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: June 19, 2019)
Increase in Lean Appendicular Muscle Mass by more than 10% in both groups [ Time Frame: 24 weeks ]
Original Primary Outcome Measures  ICMJE Same as current
Change History Complete list of historical versions of study NCT03995251 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures  ICMJE
 (submitted: August 20, 2019)
  • Improvement by 10 % in Hand Grip strength in both groups [ Time Frame: 24 weeks ]
  • Improvement by 10 % in6 minute walk distance in both groups [ Time Frame: 24 weeks ]
  • Improvement by 10 % in the increased bone and muscle mass in both groups [ Time Frame: 24 weeks ]
  • Improvement by 10 % L3 Skeletal Muscle Index in both groups. [ Time Frame: 24 weeks ]
  • Improvement by 10 % in serum ammonia levels in both groups [ Time Frame: 24 weeks ]
  • Improvement by 10 % in muscle fibres on Biopsy in both groups • [ Time Frame: 24 weeks ]
  • Reduction in Myostatin level in both groups [ Time Frame: 24 weeks ]
  • Improvement in MELD scores in both groups [ Time Frame: 24 weeks ]
  • Decrease in mortality over 6 months in both groups [ Time Frame: 24 weeks ]
  • Changes in HBA1C level in both groups [ Time Frame: 24 weeks ]
  • Reduction in requirement of hospital admissions in both groups [ Time Frame: 24 weeks ]
  • Decrease in TNF alpha levels in both groups [ Time Frame: 24 weeks ]
Original Secondary Outcome Measures  ICMJE Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Efficacy and Safety of Testosterone Therapy in Improving Sarcopenia in Men With Cirrhosis.
Official Title  ICMJE Efficacy and Safety of Testosterone Therapy in Improving Sarcopenia in Men With Cirrhosis a Randomized Controlled Trial
Brief Summary
  • Study Population- Patient with cirrhosis with any aetiology with sarcopenia visiting ILBS OPD/IPDs who are willing to visit ILBS gymnasium twice weekly for first month.
  • Study Design- A Prospective Randomized Controlled Trial
  • Study Period- Study will be conducted at ILBS from April 2019 to Oct 2019

    • Sample Size:As shown by Eva Roman et al - in cirhotics with sarcopenia exercise increases mean lean appendicular mass , by 0.38 kg (14 patients, p < 0.03), and Sinclair et al has shown testosterone (22 patients, p <0.05)) to increase mean Appendicular lean mass by +1.69 kg - for 10% increase in APLM
    • we need to enroll 40 patients in each arm, and considering a los to follow up approx.10% , will require minimum 44 patients in each arm
    • We will therefore enroll and randomize 100 patients with 50 in each arm.

Intervention - Testosterone Supplementation - Intramuscular Testosterone Undecanoate 1000 Mg (4 ml volume in oily base) will be injected into the upper, outer quadrant of the buttock at 0, 6, 12,16,20, 24 weeks according to manufacturer recommendations.

Monitoring and assessment - On every visit patient will be inquired or evaluated for side effects like local site pain or hematoma , hypertension, headache, allergic reactions, acne, nausea , mood swings, pedal edema , breast enlargement and others.

Detailed Description Not Provided
Study Type  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Condition  ICMJE Liver Cirrhosis
Intervention  ICMJE
  • Drug: Testosterone Supplementation
    Intramuscular Testosterone Undecanoate 1000 Mg (4 ml volume in oily base) will be injected into the upper, outer quadrant of the buttock at 0, 6, 12,16,20, 24 weeks according to manufacturer recommendations
  • Drug: Standard Medical Treatment
    Standard Medical Treatment
  • Other: Exercise
    Exercise
Study Arms  ICMJE
  • Experimental: Standard Medical Treatment +Intramuscular Testosterone + Exerc
    Intramuscular Testosterone Undecanoate 1000 Mg (4 ml volume in oily base) will be injected into the upper, outer quadrant of the buttock at 0, 6, 12,16,20, 24 weeks according to manufacturer recommendations
    Interventions:
    • Drug: Testosterone Supplementation
    • Drug: Standard Medical Treatment
    • Other: Exercise
  • Active Comparator: Standard Medical Treatment+Exercise
    Standard Medical Treatment +Exercise
    Interventions:
    • Drug: Standard Medical Treatment
    • Other: Exercise
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Unknown status
Estimated Enrollment  ICMJE
 (submitted: June 19, 2019)
100
Original Estimated Enrollment  ICMJE Same as current
Estimated Study Completion Date  ICMJE June 30, 2020
Estimated Primary Completion Date June 30, 2020   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • Men with cirrhosis of any etiology
  • Sarcopenia
  • CTP 6-12

Exclusion Criteria:

  • Hepatocellular carcinoma
  • Other known malignancy,
  • CTP > 12
  • Acute liver injury
  • Prostate disease,
  • Known hypersensitivity to testosterone therapy,
  • Polycythaemia (haematocrit >55%),
  • Uncontrolled hypertension (>160/90 mmHg despite treatment),
  • Uncontrolled obstructive sleep apnoea,
  • Severe renal dysfunction (estimated glomerular filtration rate <30ml/min)
  • Uncontrolled epilepsy, migraine, or significant cardiac insufficiency (New York Heart Association class III or IV or LVEF < 45-50%.
  • CKD (Chronic Kidney Disease) - eGFR (Glomerular Filtration Rate) <60%
  • Platelet count below 30,000 or taking warfarin
  • Failure to give consent.
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Gender Based Eligibility: Yes
Gender Eligibility Description: Males only
Ages  ICMJE 18 Years to 55 Years   (Adult)
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE India
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT03995251
Other Study ID Numbers  ICMJE ILBS-Cirrhosis-21
Has Data Monitoring Committee No
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement  ICMJE
Plan to Share IPD: Undecided
Responsible Party Institute of Liver and Biliary Sciences, India
Study Sponsor  ICMJE Institute of Liver and Biliary Sciences, India
Collaborators  ICMJE Not Provided
Investigators  ICMJE Not Provided
PRS Account Institute of Liver and Biliary Sciences, India
Verification Date June 2019

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP