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Stem Cell Treatment of Peyronie´s Disease.

Treatment With Stromal Vascular Fraction of Peyronie´s Disease in Humans

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04771442
Enrollment
22
Registered
2021-02-25
Start date
2022-09-09
Completion date
2024-05-30
Last updated
2024-07-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Penile Diseases, Penile Induration

Keywords

Stromal vascular fraction, Peyronie´s disease, Peyronie´s disease questionnaire, Erectile dysfunction

Brief summary

Purpose of the project is to investigate if a single injection of autologous stromal vascular fraction into and around plaque is a safe and suitable treatment. Twentythree men \> 18 years with Peyronie´s Disease in the chronic phase will be recruited. The operative same-day procedure will be performed in general anaesthesia by a plastic surgeon. Before the patient wake, local anaesthesia is put around the penis. Processed stem cells are injected into the plaque/fibrosis subcutaneously. There will be a follow up at 1, 3, 6, 12 months. It is a pilot study with no randomisation. The group will be compared to a historical control group.

Interventions

Sponsors

Odense University Hospital
CollaboratorOTHER
Esbjerg Hospital - University Hospital of Southern Denmark
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Acquired penile curvature \>30 and \<90 degrees associated with a palpable penile plaque on physical examination. 2. One or several plaques at ultrasound screening. 3. Willingness to attend follow-up at 1, 3, 6 and 12 months. 4. Understand and speak Danish. 5. Men \> 18 years of age

Exclusion criteria

Patients may not be: 1. Taking the medication Coumadin, Warfarin or NOAK (new oral anticoagulant). 2. Unable to achieve adequate erection with penile injection to access degree of curvature. 3. Undergoing definitive treatment for prostate cancer, bladder cancer, or other pelvic malignancies including surgery, external beam radiation therapy, brachytherapy, and cryotherapy. 4. With prior history of prostate cancer, hematologic disorders, chronic liver disease including cirrhosis and hepatitis C, disorders affecting the immune system, including infection with the human immunodeficiency virus, or psychiatric disorders including but not limited to major depression, schizophrenia, bipolar disease. 5. With a history of cerebrovascular incidents, a history of deep venous thrombosis within the past 5 years or a history of untreated or severe sleep apnoea. 6. With a clinically significant abnormal, results that would put the subject at increased risk or compromise the integrity of the study data, in the opinion of the investigator. Blood tests will be analysed for HIV, Hepatitis B and C and syphilis and those applicable within guidelines of the department. 7. Involved with any other projects with an investigational drug within 30 days. 8. In treatment for alcohol or drug abuse within six months. 9. With congenital deviation of penis. 10. Within six months treated with Collagenase, ESWT and/or other therapeutic injection in the plaque treatment for PD.

Design outcomes

Primary

MeasureTime frameDescription
Change in the bend of the erect penis[measured at baseline, 1, 3, 6, 12 months]Changes in degrees measured with a goniometer compared to baseline

Secondary

MeasureTime frameDescription
Change in Peyronie´s disease questionnaire bother symptoms[measured at baseline, 1, 3, 6, 12 months]Will there be less bother symptoms compared to baseline? Score 0-44. The higher the score the more symptoms.
Change in International Index of Erectile Function score,[measured at baseline, 1, 3, 6, 12 months].Score can be 5-25, the higher the score the less symptoms. Answers are compared to baseline.
Change in stretched Penile Length from symphysis to meatus of the glans (cm)[measured at baseline, 1, and 12 months]Ruler
Change in penile Plaque size (mm3)[measured at baseline, 1, and 12 months]Ultrasonic scanner

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026