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

Primary Purpose

Liver Cirrhosis

Status
Unknown status
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Testosterone Supplementation
Standard Medical Treatment
Exercise
Sponsored by
Institute of Liver and Biliary Sciences, India
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Liver Cirrhosis

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Institute of Liver & Biliary SciencesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Standard Medical Treatment +Intramuscular Testosterone + Exerc

Standard Medical Treatment+Exercise

Arm Description

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

Standard Medical Treatment +Exercise

Outcomes

Primary Outcome Measures

Increase in Lean Appendicular Muscle Mass by more than 10% in both groups

Secondary Outcome Measures

Improvement by 10 % in Hand Grip strength in both groups
Improvement by 10 % in6 minute walk distance in both groups
Improvement by 10 % in the increased bone and muscle mass in both groups
Improvement by 10 % L3 Skeletal Muscle Index in both groups.
Improvement by 10 % in serum ammonia levels in both groups
Improvement by 10 % in muscle fibres on Biopsy in both groups •
Reduction in Myostatin level in both groups
Improvement in MELD scores in both groups
Decrease in mortality over 6 months in both groups
Changes in HBA1C level in both groups
Reduction in requirement of hospital admissions in both groups
Decrease in TNF alpha levels in both groups

Full Information

First Posted
June 19, 2019
Last Updated
August 20, 2019
Sponsor
Institute of Liver and Biliary Sciences, India
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1. Study Identification

Unique Protocol Identification Number
NCT03995251
Brief Title
Efficacy and Safety of Testosterone Therapy in Improving Sarcopenia in Men With Cirrhosis.
Official Title
Efficacy and Safety of Testosterone Therapy in Improving Sarcopenia in Men With Cirrhosis a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2019
Overall Recruitment Status
Unknown status
Study Start Date
July 4, 2019 (Actual)
Primary Completion Date
June 30, 2020 (Anticipated)
Study Completion Date
June 30, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institute of Liver and Biliary Sciences, India

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Cirrhosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard Medical Treatment +Intramuscular Testosterone + Exerc
Arm Type
Experimental
Arm Description
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
Arm Title
Standard Medical Treatment+Exercise
Arm Type
Active Comparator
Arm Description
Standard Medical Treatment +Exercise
Intervention Type
Drug
Intervention Name(s)
Testosterone Supplementation
Intervention Description
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
Intervention Type
Drug
Intervention Name(s)
Standard Medical Treatment
Intervention Description
Standard Medical Treatment
Intervention Type
Other
Intervention Name(s)
Exercise
Intervention Description
Exercise
Primary Outcome Measure Information:
Title
Increase in Lean Appendicular Muscle Mass by more than 10% in both groups
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
Improvement by 10 % in Hand Grip strength in both groups
Time Frame
24 weeks
Title
Improvement by 10 % in6 minute walk distance in both groups
Time Frame
24 weeks
Title
Improvement by 10 % in the increased bone and muscle mass in both groups
Time Frame
24 weeks
Title
Improvement by 10 % L3 Skeletal Muscle Index in both groups.
Time Frame
24 weeks
Title
Improvement by 10 % in serum ammonia levels in both groups
Time Frame
24 weeks
Title
Improvement by 10 % in muscle fibres on Biopsy in both groups •
Time Frame
24 weeks
Title
Reduction in Myostatin level in both groups
Time Frame
24 weeks
Title
Improvement in MELD scores in both groups
Time Frame
24 weeks
Title
Decrease in mortality over 6 months in both groups
Time Frame
24 weeks
Title
Changes in HBA1C level in both groups
Time Frame
24 weeks
Title
Reduction in requirement of hospital admissions in both groups
Time Frame
24 weeks
Title
Decrease in TNF alpha levels in both groups
Time Frame
24 weeks

10. Eligibility

Sex
All
Gender Based
Yes
Gender Eligibility Description
Males only
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility 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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dr Shushrut Singh, MD
Phone
01146300000
Email
drsushrut20@gmail.com
Facility Information:
Facility Name
Institute of Liver & Biliary Sciences
City
New Delhi
State/Province
Delhi
ZIP/Postal Code
110070
Country
India
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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

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