peyronie disease. induratio penis plastica
Conditions
Interventions
patients were treated with 100 unith of botox in 5cc of normal saline (intralesional ).
Treatment - Drugs
patients were treated with 100 unith of botox in 5cc of normal saline (intralesional )
Sponsors
Research Deputy of Ahvaz University of Medical Science and Health science
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: Inclusion criterion: stable peyronie plaque. Exclusion criteria : active phase of peyronie disease; less than 1 year history of peyronie disease and allegy to botox
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Size of plaque. Timepoint: preinjection and postinjection(8,16 weeks later ). Method of measurement: with sonography , milimeter.;Penile curvature. Timepoint: preinjection and postinjection(8,16 weeks later ). Method of measurement: with photography , degree.;Imprvement of sexual intercourse. Timepoint: preinjection and postinjection(8,16 weeks later ). Method of measurement: clinical. | — |
Secondary
| Measure | Time frame |
|---|---|
| Side effect. Timepoint: preinjection and post injection (8 ,16 weeks later ). Method of measurement: clinical. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Mehdi Yazdinejad
Ahvaz Jundishapour University of Medical Sciences
Outcome results
None listed