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Completed

NCT Number: NCT01143818

ESPRIT Study in Hypogonadal Men

Observational study with AndroGel®, Testosterone 1% gel therapy (ESPRIT) in hypogonadal men in the community over 6 months.

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Observational

Primary location

Site Ref # / Investigator 59749, Burnaby, British Columbia, Canada

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About this study

The objective of this study was to evaluate the efficacy and safety of AndroGel (testosterone gel) 1% following administration in community dwelling men with hypogonadism. The percent change from baseline to Month 6 in aging male symptom (AMS) assessment was the primary endpoint. Secondary endpoints were changes from baseline to Month 6 in International Index of Erectile Dysfunction (IIEF), Multidimensional Fatigue Inventory (MFI), and body mass index (BMI) assessments.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male patients >= 18 years of age
  • Hypogonadism not previously treated with testosterone
  • Testosterone deficiency confirmed clinically and biochemically
  • Being prescribed AndroGel® 1% in accordance with the local summary of product characteristics

Exclusion criteria

  • According to the contra-indications,
  • Unwilling or unable to sign informed consent form

Treatment and study plan

AndroGel (testosterone gel) 1%

Drug

AndroGel is topical testosterone gel 1% and is prescribed for once daily use.

Other names: Topical AndroGel, 1% AndroGel, AndroGel®

Primary outcomes

  1. Percent Change From Baseline to Month 6 in Aging Male Symptoms (AMS) in Mean Total Score

    Time frame: Baseline to Month 6

    The Aging Male Symptoms (AMS) test is self-administered and designed to assess symptoms of aging with a rating from none (0) to extremely severe (5) for 17 items from psychological (5 items), somatic (7 items), and sexual (5 items) categories. Total scores range from 17 (minimum) to 85 (maximum). The AMS total score was reported at baseline and at Month 6 and represented the sum of all the items. The percent change from baseline was calculated as the [(AMS value at Month 6 - AMS value at baseline)/baseline value] x 100.

Secondary outcomes

  1. Percent Change From Baseline to Month 6 in the International Index of Erectile Function (IIEF) Total Score

    Time frame: Baseline to Month 6

    The International Index of Erectile Function (IIEF) test is a validated 15 question assessment designed to measure changes in erectile function (6 items), orgasmic function (2 items), sexual desire (2 items), intercourse satisfaction (3 items), and overall satisfaction (2 items). The scores ranged from 0 to 5 on each item with a lower score indicating greater dysfunction. A total IIEF score of 0 (minimum) to 75 (maximum) was possible and represented the sum of all the items at baseline and Month 6. The percent change = [(IIEF value at Month 6-IIEF baseline value)/IIEF baseline value]x 100.

  2. Percent Change From Baseline to Month 6 in the Multidimensional Fatigue Inventory (MFI) Total Score

    Time frame: Baseline to Month 6

    The MFI is a 20-item self-reported instrument designed to measure fatigue. Five scales measure different modes of fatigue: general fatigue (4 items), physical fatigue (4 items), mental fatigue (4 items), reduced motivation (4 items), and reduced activity items (4 items). The scores for each item range from 1 to 5. Each subscale includes 4 items with 5-point Likert scales and subscale scores range from 4 to 20 with a higher score indicating greater fatigue. The percent change=[(MFI value at Month 6-MFI value at baseline)/MFI baseline value] X 100.

  3. Percent Change From Baseline to Month 6 in Body Mass Index (BMI)

    Time frame: Baseline to Month 6

    The BMI was measured in kg/m^2 and was reported at baseline and at the Month 6. BMI = weight (kg)/[(height (m) x height (m)] and was measured to 1 decimal point precision.

Sponsors and collaborators

Lead sponsor

Abbott

Industry

Collaborators

  • Fovea

Registry information

Official study title

Energy, Sexual Desire and Body PropoRtions wIth AndroGel®, Testosterone 1% Gel Therapy (ESPRIT) in Hypogonadal Men

Important dates

Study start
2007
Primary completion
2010
Study completion
2010
First posted
Jun 14, 2010
Registry last updated
Oct 17, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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