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CompletedNCT04350125

PRP for the Treatment of Erectile Dysfunction (ED)

A Pilot Study Evaluating the Use of Autologous Platelet-rich Plasma (PRP) for the Treatment of Erectile Dysfunction

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
4 (actual)
Sponsor
Mayo Clinic · Academic / Other
Sex
Male
Age
45 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Researchers are trying to determine the safety and efficacy of Platelet Rich Plasma (PRP) in the treatment of Erectile Dysfunction (ED).

Conditions

Interventions

TypeNameDescription
BIOLOGICALAutologous Platelet Rich PlasmaOne 4-5mL platelet rich plasma injection administered to each side of the intracavernosal space on the right and left side of the corpus cavernosum at the base of the penis, every two weeks for 6 weeks.

Timeline

Start date
2022-03-04
Primary completion
2023-10-23
Completion
2023-10-23
First posted
2020-04-16
Last updated
2023-10-27

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04350125. Inclusion in this directory is not an endorsement.

PRP for the Treatment of Erectile Dysfunction (ED) (NCT04350125) · Clinical Trials Directory