Acne vulgaris and male sexual dysfunction
Conditions
Interventions
Group 1: normal males not receiving isotretinion (control group)
Group 2: male patient receiving isotretinion for 2 months.
Group 3: male patient receiving isotretinion for 4 months
Group 4: male pat
Sponsors
Cairo university
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: Males with severe nodulocystic acne
Exclusion criteria
Exclusion criteria: Any male with systemic illnesses or receiving medication causing erectile dysfunction or affecting his desire
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To identify the presence of sexual dysfunction in male patients receiving isotretinion for treatment of acne vulgaris. Assessment of the severity of acne. | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate relationship of male sexual dysfunction & symptoms of anxiety and depression in males caused by acne vulgaris and isotretinion treatment. To evaluate the effect of isotretinion on male sexual desire | — |
Countries
Africa
Contacts
Public ContactSameh GamalEl Din
Cairo University Andrology & STDs
Outcome results
None listed