Short-term Effects of Aromatase Inhibition in Obese Men
Primary Purpose
Hypogonadotrophic Hypogonadism, Obesity
Status
Completed
Phase
Phase 3
Locations
Netherlands
Study Type
Interventional
Intervention
Letrozole (Femara)
Sponsored by
About this trial
This is an interventional treatment trial for Hypogonadotrophic Hypogonadism focused on measuring obesity, Hypogonadotrophic hypogonadism, aromatase inhibition
Eligibility Criteria
Inclusion Criteria: BMI between 35 and 50 Male sex Ages between 20 and 50 Serum total testosterone under 10 nmol/l Serum luteinizing hormone (LH) under 9 mU/l Serum estradiol over 40 pmol/l Exclusion Criteria: Comorbidity Serum prostate-specific antigen (PSA) over 4.0 U/l Discontinuation of smoking less than six months ago Medication known to affect hormonal parameters
Sites / Locations
- Rijnstate Hospital
Outcomes
Primary Outcome Measures
Body weight
Body mass index (BMI)
Waist circumference
Body composition
Exercise capacity
Serum levels of hormones
Glucose tolerance
Reported side effects
Psychological characteristics (Symptom Checklist, intelligence quotient [IQ] NPV)
Secondary Outcome Measures
Lipid profile
Blood counts
Bone markers
Liver enzymes
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00138710
Brief Title
Short-term Effects of Aromatase Inhibition in Obese Men
Official Title
Short-term Effects of Aromatase Inhibition in Obese Men
Study Type
Interventional
2. Study Status
Record Verification Date
October 2010
Overall Recruitment Status
Completed
Study Start Date
August 2005 (undefined)
Primary Completion Date
January 2010 (Actual)
Study Completion Date
January 2010 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Rijnstate Hospital
4. Oversight
5. Study Description
Brief Summary
In this study, 50 obese men with a hormonal imbalance will be treated with letrozole or placebo for six months in order to examine the effects on the hormonal balance, and on weight loss. The study will also address the side effects and psychological effects of letrozole as compared to placebo.
Detailed Description
The aim of the study is to establish the short-term efficacy and safety of aromatase inhibition in restoring and maintaining eugonadism in hypogonadotrophic hypogonadal men. Secondary aim is to detect the short-term somatic and psychological effects.
Study design: Double blind randomized placebo-controlled trial.
Treatment: 26 weeks of either letrozole or placebo. All patients will start on 1 tablet per week, dose adjustments will be performed if serum testosterone or estradiol are outside the target range. All men will be prescribed a mildly hypocaloric diet.
Endpoints: BMI, body weight, waist circumference, body composition, exercise capacity, serum levels of several hormone markers, glucose tolerance, psychological characteristics.
All patients will be measured 6 times during the study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypogonadotrophic Hypogonadism, Obesity
Keywords
obesity, Hypogonadotrophic hypogonadism, aromatase inhibition
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Letrozole (Femara)
Primary Outcome Measure Information:
Title
Body weight
Title
Body mass index (BMI)
Title
Waist circumference
Title
Body composition
Title
Exercise capacity
Title
Serum levels of hormones
Title
Glucose tolerance
Title
Reported side effects
Title
Psychological characteristics (Symptom Checklist, intelligence quotient [IQ] NPV)
Secondary Outcome Measure Information:
Title
Lipid profile
Title
Blood counts
Title
Bone markers
Title
Liver enzymes
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
BMI between 35 and 50
Male sex
Ages between 20 and 50
Serum total testosterone under 10 nmol/l
Serum luteinizing hormone (LH) under 9 mU/l
Serum estradiol over 40 pmol/l
Exclusion Criteria:
Comorbidity
Serum prostate-specific antigen (PSA) over 4.0 U/l
Discontinuation of smoking less than six months ago
Medication known to affect hormonal parameters
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hans de Boer, MD PhD
Organizational Affiliation
Rijnstate Hospital, Arnhem, the Netherlands
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rijnstate Hospital
City
Arnhem
ZIP/Postal Code
6815 AM
Country
Netherlands
12. IPD Sharing Statement
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Short-term Effects of Aromatase Inhibition in Obese Men
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