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Phase 2 N=6 Randomized Quadruple-blind Treatment

Pilot Study of Losartan and N-acetylcysteine as Inhibitors of Muscle Oxidative Stress in Elderly

Aging

Enrolled (actual)
6
Serious AEs
0.0%
Results posted
May 2018
Primary outcome: Primary: Leg Blood Flow as Measured by Doppler Ultrasound — 174.99; 102.08; 428.45 ml/minute

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
N-acetylcysteine (Drug); Losartan (Drug); Placebo losartan (Drug); Placebo N-acetylcysteine (Drug)
Age
Adult, Older Adult · 60+ yrs
Sex
All
Sponsor
The University of Texas Medical Branch, Galveston
Primary completion
May 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
Leg Blood Flow as Measured by Doppler Ultrasound
70.60; 128.78; 57.79
PRIMARY
Leg Blood Flow as Measured by Doppler Ultrasound
70.60; 128.78; 57.79
PRIMARY
Leg Blood Flow as Measured by Doppler Ultrasound
70.60; 128.78; 57.79
PRIMARY
Leg Blood Flow as Measured by Doppler Ultrasound
70.60; 128.78; 57.79
PRIMARY
Leg Blood Flow as Measured by Doppler Ultrasound
70.60; 128.78; 57.79
PRIMARY
Leg Blood Flow as Measured by Doppler Ultrasound
70.60; 128.78; 57.79
PRIMARY
Leg Blood Flow as Measured by Doppler Ultrasound
70.60; 128.78; 57.79
SECONDARY
Handgrip Strength of Dominant Hand as Measured by Handgrip Dynamometry at 50% Perceived Effort at Baseline
21.5; 23.2; 20.5
SECONDARY
Handgrip Strength of Non-dominant Hand as Measured by Handgrip Dynamometry at 50% Perceived Effort at Baseline
24.2; 19.3; 17.0
SECONDARY
Handgrip Strength of Dominant Hand as Measured by Handgrip Dynamometry at 100% Effort at Baseline
45.2; 33.2; 28.8
SECONDARY
Handgrip Strength of Non-dominant Hand as Measured by Handgrip Dynamometry at 100% Effort at Baseline
47.1; 31.1; 26.5
SECONDARY
Handgrip Fatigue of Dominant Hand as Measured by Handgrip Dynamometry at Baseline
129.6; 94.2; 103.4
SECONDARY
Handgrip Fatigue of Non-dominant Hand as Measured by Handgrip Dynamometry at Baseline
64.55; 83.62; 90.29
SECONDARY
Handgrip Strength of Dominant Hand as Measured by Handgrip Dynamometry at 50% Perceived Effort After All Doses of Study Intervention
21.2; 15.8; 16.2
SECONDARY
Handgrip Strength of Non-dominant Hand as Measured by Handgrip Dynamometry at 50% Perceived Effort After All Doses of Study Intervention
17.8; 14.8; 13.7
SECONDARY
Handgrip Strength of Dominant Hand as Measured by Handgrip Dynamometry at 100% Perceived Effort After All Doses of Study Intervention
44.1; 31.3; 24.2
SECONDARY
Handgrip Strength of Non-dominant Hand as Measured by Handgrip Dynamometry at 100% Perceived Effort After All Doses of Study Intervention
42.3; 28.6; 30.2
SECONDARY
Handgrip Fatigue of Dominant Hand as Measured by Handgrip Dynamometry After All Doses of Study Intervention
101.0; 95.97; 111
SECONDARY
Handgrip Fatigue of Non-dominant Hand as Measured by Handgrip Dynamometry After All Doses of Study Intervention
88.61; 93.25; 95.60
SECONDARY
Personal Perceptual Fatigue Measured by Multidimensional Fatigue Symptom Inventory - Subscale General Fatigue at Baseline
0; 1.5; 3.5
SECONDARY
Personal Perceptual Fatigue Measured by Multidimensional Fatigue Symptom Inventory - Subscale General Fatigue After All Doses of Study Intervention
0; 2; 6.5
SECONDARY
Personal Perceptual Fatigue Measured by Multidimensional Fatigue Symptom Inventory - Subscale Physical Fatigue at Baseline
0.5; 0.5; 3
SECONDARY
Personal Perceptual Fatigue Measured by Multidimensional Fatigue Symptom Inventory - Subscale Physical Fatigue After All Doses of Study Intervention
0; 0.5; 7
SECONDARY
Personal Perceptual Fatigue Measured by Multidimensional Fatigue Symptom Inventory - Subscale Emotional Fatigue at Baseline
0.5; 0; 4
SECONDARY
Personal Perceptual Fatigue Measured by Multidimensional Fatigue Symptom Inventory - Subscale Emotional Fatigue After All Doses of Study Intervention
0.5; 0; 7.5
SECONDARY
Personal Perceptual Fatigue Measured by Multidimensional Fatigue Symptom Inventory - Subscale Mental Fatigue at Baseline
0.5; 0.5; 4.5
SECONDARY
Personal Perceptual Fatigue Measured by Multidimensional Fatigue Symptom Inventory - Subscale Mental Fatigue After All Doses of Study Intervention
0; 1; 6.5
SECONDARY
Personal Perceptual Fatigue Measured by Multidimensional Fatigue Symptom Inventory - Subscale Vigor Fatigue at Baseline
18; 15; 16.5
SECONDARY
Personal Perceptual Fatigue Measured by Multidimensional Fatigue Symptom Inventory - Subscale Vigor Fatigue After All Doses of Study Intervention
20.5; 15.5; 14
SECONDARY
Personal Perceptual Fatigue Measured by Multidimensional Fatigue Symptom Inventory - Total Score at Baseline
-16.5; -12.5; -1.5
SECONDARY
Personal Perceptual Fatigue Measured by Multidimensional Fatigue Symptom Inventory - Total Score After All Doses of Study Intervention
-20; -12; 13.5
SECONDARY
Global Fatigue Score as Measured by Brief Fatigue Inventory at Baseline
0.55; 0.38; 1.11
SECONDARY
Global Fatigue Score as Measured by Brief Fatigue Inventory After Study Invention
0.5; 0.22; 1.19
SECONDARY
Perceptual Fatigue of Non-dominant Arm as Measured by Visual Analog Scale Before Handgrip Fatigue Test at Baseline.
0.3; 3.3; 0.2
SECONDARY
Perceptual Fatigue of Non-dominant Arm as Measured by Visual Analog Scale After Handgrip Fatigue Test at Baseline.
2.7; 7.5; 0.6
SECONDARY
Perceptual Fatigue of Non-dominant Arm as Measured by Visual Analog Scale Before Handgrip Fatigue Test After Study Intervention
1.45; 1; 0.65
SECONDARY
Perceptual Fatigue of Non-dominant Arm as Measured by Visual Analog Scale After Handgrip Fatigue Test After Study Intervention
3.4; 11; 0.75
SECONDARY
Perceptual Fatigue of Whole Body as Measured by Visual Analog Scale Before Handgrip Fatigue Test at Baseline.
0.4; 1.15; 0.55
SECONDARY
Perceptual Fatigue of Whole Body as Measured by Visual Analog Scale After Handgrip Fatigue Test at Baseline.
1.05; 5; 0.6
SECONDARY
Perceptual Fatigue of Whole Body as Measured by Visual Analog Scale Before Handgrip Fatigue Test After Study Intervention
0.7; 4.1; 0.55
SECONDARY
Perceptual Fatigue of Whole Body as Measured by Visual Analog Scale After Handgrip Fatigue Test After Study Intervention
1.25; 5.3; 0.95

Summary

The general hypothesis is that elderly have diminished nutritive flow to skeletal muscle and impaired capacity for building muscle. In aging populations, this decreased ability to build muscle may represent a tipping point in the progression towards chronic physical frailty and disability. The goal is to examine whether novel pharmacologic therapies can improve nutritive blood flow to the muscles and muscle building in the elderly. The purpose of this study is 1) to determine if losartan administration will enhance blood flow and 2) to determine if N-acetylcysteine (NAC) will enhance blood flow. The investigators will study community dwelling, healthy older men and women (60-85 years). Subjects will be randomized to one of three groups: Experimental Group 1: Placebo losartan and placebo N-acetylcysteine (NAC). Experimental Group 2: losartan (25mg/dose) and placebo N-acetylcysteine (NAC). Experimental Group 3: N-acetylcysteine (NAC) (50 mg/kg/dose) and placebo Subjects will admit to the clinic on day 1 of the study. Baseline testing consisting of leg blood flow (LBF), contrast enhanced ultrasound, handgrip testing and fatigue questionnaires. After testing is completed the subjects will recieve their first dose of NAC/ losartan/ placebo with dinner. Subjects will be fasted after 10 pm. On day 2, leg blood flow (LBF) will be measured approximately 12 hours post dose 1. Subjects will receive their second dose of NAC/ losartan/ placebo. Leg blood flow will be measured 1 hour and 2 hours post dose 2 of study interventions. The subjects will eat a meal and receive their third dose of the study intervention. Leg blood flow will be repeated at 1 hour and 2 hours post dose 3. Appoximately 30 minutes after dose 3 of the study intervention, handgrip testing will be performed and fatigue questionnaires completed.

Eligibility Criteria

Inclusion Criteria

  • Age between 60-85 years.
  • Ability to sign informed consent.
  • Ability to sign consent form.
  • Ability to pass a mini-mental status exam (score >23 on the 30-item Mini Mental State Examination, MMSE).
  • Free-living, prior to admission.

Exclusion Criteria

  • Subjects with cardiac abnormalities considered exclusionary by the study physicians (e.g., unstable angina or a cardiology-confirmed ECG that demonstrates cardiac abnormalities such as > 0.2 mV horizontal or downsloping ST segment depression, frequent arrhythmia's (> 10 PVC/min), or valvular disease).
  • Subjects with uncontrolled metabolic disease, including liver or renal disease.
  • Subjects with vascular disease characterized by a combination of risk factors of peripheral atherosclerosis. (e.g., uncontrolled hypertension, obesity, uncontrolled diabetes, hypercholesterolemia > 250 mg/dl, claudication or evidence of venous or arterial insufficiency upon palpitation of femoral, popliteal, and pedal arteries.
  • Any history of hypo- or hyper-coagulation disorders. (e.g., Coumadin use or history of DVT or PE).
  • Subjects with chronically elevated systolic pressure >170 or a diastolic blood pressure > 100. Subjects may be included if they are taking medication and have a blood pressure below these criteria.
  • Subjects with cancer or recently (6 months) treated cancer other than basal cell carcinoma.
  • Any subject currently on a weight-loss diet or a body mass index > 33 kg/m2.
  • Inability to abstain from smoking for duration of study.
  • A history of > 20 pack per year smoking.
  • Subjects with atrial fibrillation, history of syncope, angina, or congestive heart failure.
  • Any subject that is HIV-seropositive or has active hepatitis.
  • Recent anabolic or corticosteroids use (within 3 months).
  • Subjects with low hemoglobin or hematocrit (i.e., lower than accepted lab values).
  • Agitation/aggression disorder.
  • Dementia.
  • History of stroke with motor disability.
  • A recent history ( 2/year).
  • Depression (>5 of the 15 items on the Geriatric Depression Scale (GDS).
  • Subjects suffering malnutrition or with a BMI < 20 kg/m2 with low albumin or transferrin.
  • Asthma
  • Any other condition or event considered exclusionary by the PI and covering faculty physician.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01384591). 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.

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