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Quality of Life With TESTIM® (LIFE)

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Status

Completed

Conditions

Hypogonadism

Study type

Observational

Funder types

Industry

Identifiers

NCT01148433
FE999303 CS01

Details and patient eligibility

About

The present non-interventional study is to document the testosterone levels in patients with clinical symptoms such as loss of sexual desire indicating hypogonadism (testosterone deficiency syndrome). During testosterone replacement therapy with TESTIM®, the changes in the quality of life - especially with respect to motivation, activity and fatigue - of hypogonadal patients will be documented and correlated with the testosterone levels during the course of therapy.

Enrollment

157 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • therapeutic need according to SPC
  • written informed consent

Exclusion criteria

  • contraindications according to SPC

Trial design

157 participants in 1 patient group

TESTIM® - drug given by prescription
Description:
Male patients with Hypogonadism

Trial contacts and locations

64

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Data sourced from clinicaltrials.gov

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