Skip to content

Efficacy of Nd-YAG Laser with Verapamil in Peyronie’s Disease

Assessment of treatment efficacy of Nd-YAG laser beside intra lesion Verapamil injection in Peyronie’s Disease patients referring to Shohada-e-Tajrish hospital : a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201710088146N27
Enrollment
80
Registered
2017-10-13
Start date
2017-09-23
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Peyronie’s Disease. Induratio penis plastica

Interventions

Intervention 1: Intervention group: In the treatment group for 6 weeks , two sessions in a week,1064 laser with a power of 0.5 watts and a dose of 50 jules per square centimeter in an area of 1 centim
Treatment - Other
Placebo
Intervention group: In the treatment group for 6 weeks , two sessions in a week,1064 laser with a power of 0.5 watts and a dose of 50 jules per square centimeter in an area of 1 centimeter square with
Control group: The only standard treatment for verapamil injection is done and the laser probe is placed on the plaque with red light only.

Sponsors

Vice chancellor for research,Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion Criteria: All Patients with Peyronie's Disease; aged 18 years and over; have at least Peyronie's Disease for 6 months ; Exclusion criteria: Patients with a Peyronie's Disease and receive multiple treatments; Skin disorder in the penis; History of Inflammatory diseases of the skin; uncontrolled hypertension; history of heart attacks in the last one month; patients with acute phase or released fibrosis plaque during the penis; patients who are not satisfied to entering the study;

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Plaque size. Timepoint: One month and three months after the end of treatment. Method of measurement: sonography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Farzad Allameh

Laser Application Research Center in Medical Science

laser.cntr@yahoo.com+98 21 2274 9221

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026