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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05855070
Other study ID # RC 6-5-2023
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 20, 2023
Est. completion date May 20, 2024

Study information

Verified date May 2023
Source Benha University
Contact Ahmed Abou Elezz, MD
Phone 01228555403
Email ahmed.aboelezz@fmed.bu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the present study is to investigate whether intralesional injections of Hyaluronic acid in the acute phase could reduce the progression of Peyronie's disease thanks to its interference with inflammatory and pro-fibrotic processes. Therefore, a prospective, longitudinal, double-blinded, randomized clinical study, has been designed to evaluate and compare the efficacy and safety of intralesional HA as compared with the use of verapamil injection in patients affected by Peyronie's disease.


Description:

Peyronie's disease is defined as a chronic benign condition characterized by the formation of localized fibrous inelastic scars at the level of the tunica albuginea of the penis. This condition can lead to penile curvature, painful erections and erectile dysfunction. Peyronie's disease is believed to affect 3% to 9% of the male population, with a higher prevalence among patients suffering from erectile dysfunction, diabetes and cardiovascular disease . The etiology of Peyronie's disease is largely unknown. According to current popular theories, a single traumatic event or repeated microtraumas during sexual activity can lead to a low-level autoimmune response arising from a prolonged and complex inflammatory reaction of the tunica albuginea fibers,5 which leads to plaque formation. The Peyronie's disease presents 2 different phases: active or acute and stable or chronic. It is paramount to distinguish between acute and chronic phase of the condition, since management is different in the 2 phases. Plaque formation and calcification generally take place during the acute phase, which can last for up to 18 months. In the chronic phase, penile pain will be reduced, and penile deformity stabilized. Transition to the chronic phase is defined when curvature remains stable for at least 3 months. The European Association of Urology and the American Association of Urology have released clinical practice guidelines for the diagnosis, evaluation, treatment, and follow-up of patients with Peyronie's disease. Treatment of Peyronie's disease includes both medical and surgical approaches and the management is tailored to the phase of the disease, the degree of deformity, the quality of the erections and patient's choice. Conservative treatment of Peyronie's disease is focused primarily on patients in the early (acute inflammatory) stage, and surgical remediation is used to correct curvature, allow for satisfactory intercourse, and is reserved for patients who have stable disease for at least 12 months .


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 42
Est. completion date May 20, 2024
Est. primary completion date May 20, 2024
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Patient's age from >18 - 70 years old. - A palpable nodule or plaque in the tunica of the penis - Presence of pain in the flaccid state or during painful erections. - Progressive penile curvature >15° and/or penile pain in the flaccid state or at the erection in the last 12 months Exclusion Criteria: - Patient refusal. - Calcified plaques or hourglass deformity as defined at duplex Doppler ultrasonography, - Previous Peyronie's Disease therapy with oral agents or intralesional injections - Severe concomitant erectile dysfunction (International Index of Erectile Function [IIEF-5] score < 7). - Congenital penile curvature, history of previous penile surgery, a concomitant oral treatment for Peyronie's Disease.

Study Design


Intervention

Drug:
Intralesional treatment with Hyaluronic acid
Patients will receive intralesional treatment with Hyaluronic acid (0.8% highly purified sodium salt Hyaluronic acid16 mg/2 mL; Sinovial, IBSA, Lodi, Italy) weekly for 12 weeks.
Intralesional treatment with Verapamil
Patients will receive intralesional treatment with Verapamil (10 mg in 5 mL of normal saline water) weekly for 12 weeks.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Benha University

Outcome

Type Measure Description Time frame Safety issue
Primary Penile curvature degree The change from the baseline to the endpoint (12 weeks after therapy) for the penile curvature (degree). 12 weeks postoperatively
Secondary Plaque size (mm) The change in plaque size (mm) will be recorded 12 weeks postoperatively
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