A Proof of Concept Top Evaluate a Novel Penile Lengthening Protocol
Status unconfirmed
Conditions studied: Penile Elongation
In brief
The objective of this study is to examine and quantify the efficacy and safety of a new treatment protocol using platelet-rich plasma for penile length enhancement.
Key facts
- Study ID
- NCT04231422
- Run by
- Judson Brandeis
- People needed
- 30
- Starts
- 2019-11-12
- Expected to finish
- 2021-07-12
- Last updated by the study team
- 2020-01-18
Who can join
Age: 20 and older, up to 55. Sex: male. Healthy volunteers: accepted.
You may qualify if…
- Stretched penile length between 3.5 - 8.0 in
- Age 20-55 years of age
- Desire penile length elongation
- Willing to complete all aspects of combined treatment plan
- Able to measure erect penile length and mid-shaft girth at 1-month intervals
- Judged to be in good health based on medical history, physical exam, and laboratory profile
- Is willing and able to cooperate with the requirement of the study (e.g. completion of all planned study visits)
You may not qualify if…
- No prior surgical Peyronie's disease treatment
- No chordee with or without hypospadias
- No infiltration by benign or malignant mass
- No active STD
- No infiltration by an infectious agent such as lymphogranuloma venereum
- No uncontrolled psychiatric conditions
- No uncontrolled neurologic conditions
- No other uncontrolled medical conditions such as HTN or DM
- No history of spontaneous priapism
- Is unable to safely use the study devices as determined by the principal investigator
- No thrombosis of the dorsal penile artery or vein
- No known history of coagulation disorder
- No known history of stroke, bleeding, or another significant medical conditional which the investigator deems makes the subject unsuitable for enrollment in the study
- Testosterone level lower than 500
Where it is running
- BrandeisMD — San Ramon, California, United States (enrolling)
Full record on ClinicalTrials.gov
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