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Clinical Trials in Turkey / NCT06942988
Active, not recruiting Phase 3

Efficacy of Intracavernous Platelet-rich Plasma Injection in the Treatment of Erectile Dysfunction

NCT06942988 · tracked via the Priya Life Science Turkey tracker
Phase
Phase 3
Started
2023-12-29
Last updated
2025-04-24

Condition(s) studied

Erectile Dysfunction

Investigational drug(s) / intervention(s)

intracavernous platelet rich plasma therapy

intracavernous platelet rich plasma therapy: intracavernous platelet-rich plasma therapy for erectile dysfunction

Study summary

Investigation of the efficacy of autologous platelet-rich plasma administration on the potency of patients with vasculogenic and/or neurogenic erectile dysfunction

Eligibility

Sex
MALE
Min age
40 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: \- 1)40-70 years old male, sexually active heterosexual, 2) Patients with a diagnosis of mild to moderate erectile dysfunction (IIEF score between 8-21) according to the International Index of Erectile Function (IIEF) for at least 3 months, 3) Patients who cannot achieve an erection despite peroral PDE5 inhibitor and intracavernous alprostadil injection therapy Exclusion Criteria: 1. Patients with psychogenic erectile dysfunction, 2) Patients with a history of priapism, penile fracture, peyronie, penile curvature 3) Patients with a history of radical prostatectomy, 4) Patients with a history of major pelvic trauma, surgery, radiotherapy, 5) Patients with a history of malignancy affecting survival, 6) Patients with severe psychiatric illness that impairs adherence to treatment, 7) Patients with any bleeding disorder or on anti-aggregants/coagulants.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Health Sciences, Bakırköy Sadi Konuk Training and Research Hospital Istanbul Istanbul

More Bakirkoy Dr. Sadi Konuk Research and Training Hospital trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06942988 on ClinicalTrials.gov ↗ ← All trials in Turkey