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The Effects of Testosterone and Nutritional Supplementation in the Undernourished Elderly

Primary Purpose

Malnutrition, Aging

Status
Unknown status
Phase
Phase 3
Locations
Australia
Study Type
Interventional
Intervention
testosterone undecanoate
Sponsored by
University of Adelaide
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malnutrition focused on measuring testosterone, food, formulated, malnutrition, undernutrition, aging, aged, aged, 80 and over, frail elderly

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Men and women aged 65 years or older who are under-nourished, as defined by a Mini Nutritional Assessment (MNA) score <24 AND 1 or more of the following: *a body mass index (BMI) of less than 22 kg/m2; *weight loss of > 7.5% in the 3 months before enrolling in the study Living independently in the community (not in a hospital, nursing home or hostel) Understand and sign informed consent document, able to communicate with the investigator, and understand and comply with the requirements of the study. Women who are taking oestrogen or other hormone replacement therapy (HRT) may take part (see exclusion criteria for exceptions), as may women who are not taking HRT. If a woman is taking HRT she must have been on a stable dose for at least 3 months before enrolment in the study. If not on HRT, she must not have been taking it for at least 3 months before enrolment. Exclusion Criteria: Dementia as indicated by a Folstein's Mini Mental State Examination (MMSE) score of < 23 Elevated haematocrit (HCT) levels (>50%) Past or present history of prostatic cancer in men (Prostate Specific Antigen (PSA) levels [> age-related normal range and/or irregular prostate on prostate examination]) or breast cancer. Pre-existing androgenic signs or symptoms in women of concern to either subject or investigator (deep voice, hirsutism, acne, androgenic hair loss). Depression (Yesavage Geriatric Depression Scale (GDS) Score > 11) Inability to attend DEXA scan or complete other requirements of the study Significant cardiac failure (NYHA Class III and above) Significantly abnormal liver function tests (ALT, GGT, bilirubin or ALP more than 2 times the upper limit of normal) Nephrotic syndrome; 24h urine protein excretion > 3 grams (if baseline urinalysis reveals > 1+ proteinuria, quantification will be performed) AND/OR calculated creatinine clearance (by the equation of Baracskay and Jarjoura for ambulatory elderly subjects [Cr clearance = 4.4/serum creatinine (mmol/L) + (88-age)](63) < 30 ml/min) AND/OR serum creatinine concentration > 0.2mmol/l. Amputee (body mass index, creatinine clearance and body composition estimations inaccurate). Any disease, which in the opinion of the investigator is likely to lead to death within one year Testosterone or other androgen therapy (including DHEA and tibolone) in the four months before starting the study. Medication with cyclosporin or barbiturates

Sites / Locations

  • Royal Adelaide Hospital

Outcomes

Primary Outcome Measures

Days in hospital
SF-36 quality of life scores (composite physical component score and composite mental component score).

Secondary Outcome Measures

Body composition
Muscle strength
Number of falls
Functional status (living arrangements, activities of daily living and frailty scale scores)
Mortality

Full Information

First Posted
June 30, 2005
Last Updated
September 7, 2006
Sponsor
University of Adelaide
Collaborators
Organon
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1. Study Identification

Unique Protocol Identification Number
NCT00117000
Brief Title
The Effects of Testosterone and Nutritional Supplementation in the Undernourished Elderly
Official Title
The Effects of Testosterone and Nutritional Supplementation, Alone and Combined, on the Adverse Effects of Under-Nutrition in the Elderly
Study Type
Interventional

2. Study Status

Record Verification Date
September 2006
Overall Recruitment Status
Unknown status
Study Start Date
July 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
February 2007 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
University of Adelaide
Collaborators
Organon

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine what effect treatment for one year with testosterone and a nutritional supplement, alone and combined, has on the adverse effects of under-nutrition in community-dwelling older men and women.
Detailed Description
We hypothesize that oral androgen therapy and nutritional supplementation will have additive beneficial effects in older malnourished individuals living in the community; there will be a reduction in hospitalizations, falls and weight loss in association with improvements in functional measures and increases in lean body mass. The present study is designed to examine the effect of 12 months oral nutrition supplementation and androgen therapy, alone and combined, on (i) frequency and length of hospitalisations; (ii) functional status; (iii) body composition and weight; (iv) living arrangements; (v) death rate, in community dwelling under-nourished men and women, 65 years and older.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malnutrition, Aging
Keywords
testosterone, food, formulated, malnutrition, undernutrition, aging, aged, aged, 80 and over, frail elderly

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
Double
Allocation
Randomized
Enrollment
200 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
testosterone undecanoate
Primary Outcome Measure Information:
Title
Days in hospital
Title
SF-36 quality of life scores (composite physical component score and composite mental component score).
Secondary Outcome Measure Information:
Title
Body composition
Title
Muscle strength
Title
Number of falls
Title
Functional status (living arrangements, activities of daily living and frailty scale scores)
Title
Mortality

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women aged 65 years or older who are under-nourished, as defined by a Mini Nutritional Assessment (MNA) score <24 AND 1 or more of the following: *a body mass index (BMI) of less than 22 kg/m2; *weight loss of > 7.5% in the 3 months before enrolling in the study Living independently in the community (not in a hospital, nursing home or hostel) Understand and sign informed consent document, able to communicate with the investigator, and understand and comply with the requirements of the study. Women who are taking oestrogen or other hormone replacement therapy (HRT) may take part (see exclusion criteria for exceptions), as may women who are not taking HRT. If a woman is taking HRT she must have been on a stable dose for at least 3 months before enrolment in the study. If not on HRT, she must not have been taking it for at least 3 months before enrolment. Exclusion Criteria: Dementia as indicated by a Folstein's Mini Mental State Examination (MMSE) score of < 23 Elevated haematocrit (HCT) levels (>50%) Past or present history of prostatic cancer in men (Prostate Specific Antigen (PSA) levels [> age-related normal range and/or irregular prostate on prostate examination]) or breast cancer. Pre-existing androgenic signs or symptoms in women of concern to either subject or investigator (deep voice, hirsutism, acne, androgenic hair loss). Depression (Yesavage Geriatric Depression Scale (GDS) Score > 11) Inability to attend DEXA scan or complete other requirements of the study Significant cardiac failure (NYHA Class III and above) Significantly abnormal liver function tests (ALT, GGT, bilirubin or ALP more than 2 times the upper limit of normal) Nephrotic syndrome; 24h urine protein excretion > 3 grams (if baseline urinalysis reveals > 1+ proteinuria, quantification will be performed) AND/OR calculated creatinine clearance (by the equation of Baracskay and Jarjoura for ambulatory elderly subjects [Cr clearance = 4.4/serum creatinine (mmol/L) + (88-age)](63) < 30 ml/min) AND/OR serum creatinine concentration > 0.2mmol/l. Amputee (body mass index, creatinine clearance and body composition estimations inaccurate). Any disease, which in the opinion of the investigator is likely to lead to death within one year Testosterone or other androgen therapy (including DHEA and tibolone) in the four months before starting the study. Medication with cyclosporin or barbiturates
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ian M Chapman, MBBS, PhD
Organizational Affiliation
University of Adelaide
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Adelaide Hospital
City
Adelaide
State/Province
South Australia
ZIP/Postal Code
5000
Country
Australia

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The Effects of Testosterone and Nutritional Supplementation in the Undernourished Elderly

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