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Contraception in Normal and Subnormal Men

U

University Hospital Muenster

Status and phase

Terminated
Phase 2

Conditions

Healthy

Treatments

Drug: injection of hormonal male contraceptive

Study type

Interventional

Funder types

Other

Identifiers

NCT00167141
IRM 2003/21

Details and patient eligibility

About

Volunteers with normal and subnormal semen parameters receive a hormonal male contraceptive in order to investigate whether there are differences between normal and subnormal men in terms of suppressibility, rate of azoospermia and reversibility of suppression of spermatogenesis.

Full description

Volunteers with normal and subnormal semen parameters receive a hormonal male contraceptive in order to investigate whether there are differences between normal and subnormal men in terms of suppressibility, rate of azoospermia and reversibility of suppression of spermatogenesis. Twenty-five men will be recruited for each group. They will be exposed to hormonal male contraception for six months.

Enrollment

41 patients

Sex

Male

Ages

20 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Volunteers with normal and subnormal semen parameters

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

41 participants in 1 patient group

testosterone injections
Experimental group
Description:
injections of testosterone to normal men (arm 1) and two men with subnormal semen parameters (arm 2)
Treatment:
Drug: injection of hormonal male contraceptive

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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