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NCT06789510

Treatment of Peyronie's Disease With Platelet-Rich Plasma

Active, enrolled NA Last updated 13 August 2025
What this trial tests

NA trial testing Autologous Platelet Rich Plasma in Peyronies Disease in 10 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
10 March 2025
Primary endpoint
1 October 2025
1 January 2026

Quick facts

Lead sponsorHerlev Hospital
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingdouble
Primary purposetreatment
Enrollment10
Start date10 March 2025
Primary completion1 October 2025
Estimated completion1 January 2026
Sites1 location across Denmark

Drugs / interventions tested

Conditions studied

Sponsor

Herlev Hospital

Who can join

18 and older, male only, with Peyronies Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this pilot study is to optimize a planned randomized, double-blind, placebo-controlled clinical trial evaluating the effects of Platelet-Rich Plasma (PRP) intralesional injections in men affected by Peyronie's disease (PD) in the fibrotic phase. The pilot study aims to identify potential challenges in the practical execution of the clinical trial, particularly regarding PRP preparation and the blinding process. Furthermore, it seeks to evaluate the effects of PRP injections.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of Autologous Platelet Rich Plasma

Trials testing the same drug.

Other recruiting trials for Peyronies Disease

Currently open trials in the same condition.

Other Herlev Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06789510.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing