N/A
N=17
Testosterone Replacement Therapy in Advanced Chronic Kidney Disease
Kidney Failure · Kidney Diseases
Bottom Line
View on ClinicalTrials.gov: NCT00645658 ↗Enrolled (actual)
17
Serious AEs
0.0%
Results posted
Aug 2024
Primary outcome: Primary: Thigh Cross Sectional Area — 58.2 centimeters squared
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Testim, 1% testosterone gel (Drug)
- Age
- Adult, Older Adult · 45+ yrs
- Sex
- Male
- Sponsor
- Palo Alto Veterans Institute for Research
- Primary completion
- Aug 2010
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Thigh Cross Sectional Area |
58.2 | — |
| PRIMARY Lean Body Mass |
48.2 | — |
| SECONDARY Fat Mass |
21.2 | — |
| SECONDARY Quadriceps Strength |
— | — |
| SECONDARY Kidney Disease-Specific Quality of Life |
42.1 | — |
| SECONDARY Inflammatory Markers |
— | — |
| SECONDARY Muscle Atrophy Signaling Pathways |
— | — |
Summary
Muscle wasting is common in advanced chronic kidney disease (CKD) and adversely affects morbidity and mortality. In 2/3 of males with advanced CKD serum testosterone (TT) levels are reduced, and likely contributes to the wasting. As TT in relatively safe physiologic replacement doses, increases muscle mass in otherwise normal TT deficient subjects, we hypothesize that physiologic TT replacement will be effective in preventing and treating the loss of muscle mass and function in CKD patients, will improve quality of life and may reduce some cardiovascular disease (CVD) risk factors.
Eligibility Criteria
Inclusion Criteria: Inclusion criteria: CKD subjects; males with calculated GFR (MRDR equation) between 15 and 40 ml/min/1.73m2 and stable or slowly progressive renal failure (decline in function of 35), alcoholism or other recreational drug use, active heart disease, angina, uncontrolled arrhythmias or myocardial infarct within past 3 months, peripheral vascular disease with claudication, active lung, liver or GI disease, sleep apnea, medically unstable subjects and subjects who received anabolic, catabolic or cytotoxic medications during the prior 3 months. History of prostate CA, PSA >4g/ml, or advanced BPH (AUA symptom score > 21) and abnormal prostate on digital rectal examination. Bone or joint abnormalities that would preclude exercise testing.
Data sourced from ClinicalTrials.gov (NCT00645658). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.