Level C· Early human research exploring benefitsProspective StudyPubMed

Treatment with stromal vascular fraction of Peyronie's disease - a study protocol.

Wiborg MH., Krøijer R., Laursen BS., Lund L.

Prospective Study with a reported sample of 22, published in Dan Med J (2023) — summary generated from the PubMed abstract.

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Level C· Early human research exploring benefitsEvidence level of this study

Early human evidence such as case series or small samples is exploring possible benefits.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
Read the A–D evidence level guide

This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Prospective Study
Journal
Dan Med J (2023)
Country
Denmark
Reported sample size
22
Source database
PubMed
PMID
37897395
NCT
NCT04771442
Citations
1

Abstract (original English)

Introduction Peyronie´s disease is the result of an acquired fibrotic plaque in the tunica albuginea. It remains unknown why the condition appears, but it seems to affect up to 9% of all men. It can result in a debilitating curvature of the erect penis, which has extensive impact on the quality of life for many men. Thus, the disease may result in low self-esteem, depression and impaired sexual performance. Methods This is a prospective pilot study investigating the feasibility and safety of stromal vascular fraction injection into the plaque of 22 men with Peyronie´s disease in the chronic phase. The stromal vascular fraction is obtained from a small liposuction of 250 ml fat in general anaesthesia and injected the same day. Conclusion We hope to show that injection of stromal vascular fraction is safe and effective in reducing curvature in men with Peyronie´s disease. Funding The study was made possible with funding from: the Region of Southern Denmark, Louis-Hansen Fund, Lizzi and Mogens Staal Fund, Karola Jørgensen Fund, Marie and Børge Kroghs Fund, the Senior Doctors Research Fund OUH, the Fund for gentle Surgery OUH and the PhD fund of the executive board of the South West Denmark Hospital. The funding sources had no influence on the trial design, data collection, analysis or publication. Trial registration Clinicaltrials gov NCT04771442, EudraCT 2020-004297-22, Danish Me

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.

Evidence level

Early human evidence such as case series or small samples is exploring possible benefits.

How we grade evidence
MaleHumansPenile IndurationPilot ProjectsProspective StudiesQuality of LifeStromal Vascular FractionPenis

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