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Pilot Study of PEnile TRAnsplantation - Vascularized Composite Allografts

Pilot Study of PEnile TRAnsplantation - Vascularized Composite Allografts

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06781606
Acronym
PETRA-VCA
Enrollment
3
Registered
2025-01-17
Start date
2025-06-01
Completion date
2031-06-01
Last updated
2025-01-17

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

Conditions

Adults with Traumatic Penile Severe Defects, Congenital Penile Defects, Micropenis

Keywords

Penile transplatation, Vascularized Composite Allografts, Allotransplantation, En bloc harvesting, urinary function, sexual function, self-image

Brief summary

Penile transplantation (PT) has recently emerged as an option for penile reconstruction and has shown encouraging outcomes at the international level with two ongoing PT program (US, South Africa). Emergence of such option has been possible thanks to the development of vascularized composite allotransplantation and because of the important limitations of autologous reconstruction (phalloplasty). Feasibility has already been proven, but the surgical management remains in its infancy and has never been tested at a European level. Furthermore, the balance between functional improvement and immunosuppressive risk still needs to be enlightened.

Interventions

PROCEDUREPenile transplantation

The penile transplantation will take place at the Edouard Herriot hospital, part of the Hospices Civils de Lyon. It will be carried out on the same day or the day after the harvesting depending on the timing of the harvesting.

Sponsors

French Association of Urology
CollaboratorUNKNOWN
Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Prospective, multicentric, non-randomized, pilot study

Eligibility

Sex/Gender
MALE
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Patient ≥ 18 years and ≤ 60 years * Patient with traumatic penile severe defects (amputation), or congenital penile defects (micropenis) * ASA ≤ 2 * NYHA ≤ 1 * Creatinine clearance \> 60 mL/min (CKD-EPI) * Patients are willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up * Informed consent signed to participate to the study

Exclusion criteria

* Gender incongruence * Congenital penile defects resulting from exstrophy/epispadias * Penile malformation due to selh-half/self-amputation * Amputation for penile cancer * Other types of malignancy in remission for less than 5 years * Progressive malignant tumor * Presenting hepatitis B, hepatitis C, or HIV infection not controlled by appropriate anti-viral therapy * Uncontrolled arterial hypertension * Moderate renal failure : glomerular filtration rate of less than 60 mL/min per 1.73 m2 * EBV sero-negative recipient with EBV sero-positive graft, due to the risk of lymphoma * Non controlled chronic infection * Malignancy, Connective tissue disease * Amyloidosis * Unbalanced diabetes * Patient with a contraindication to performing an MRI examination * Contra-indication of Thymoglobuline: Hypersensitivity to rabbit proteins or to any of the excipients of Thymoglobuline, acute or chronic infections that contraindicate any additional immunosuppression, * Contra-inducation of tacrolimus: Hypersensitivity to tacrolimus or others macrolides, or any of the excipients of PROGRAF, * Contra-indication of Mycophenolate mofetil: in patients with hypersensitivity to mycophenolate mofetil, mycophenolic acid or any of the excipients, Hypersensitivity reactions to mycophenolate mofetil; * History of major psychiatric disorders \< 3 years (psychotic disorders, severe substance abuse, severe personality disorders) or persons under psychiatric care ; * Person deprived of their liberty by a judicial or administrative decision ; * Person admitted to a health or social institution for purposes other than research * Adult subjects to a legal protection measure (guardianship, curatorship) * Person not affiliated to a social security scheme of beneficiaries of a similar scheme

Design outcomes

Primary

MeasureTime frameDescription
Complete functional evaluation24 monthsComplete functional evaluation after penile transplantation, including the different function of the phallus : Urinary function (uroflowmetry, post-voiding residual voluma and Urinary Symptom Profile (USP®) );

Secondary

MeasureTime frameDescription
Complete functional evaluationPreoperatively, 6 months and 12 monthsComplete functional evaluation after penile transplantation, including the different function of the phallus : Urinary function (uroflowmetry, post-voiding residual voluma and Urinary Symptom Profile (USP®) );
Postoperative complicationsup to 60 monthsAny surgical complications which occur in the first three months post transplantation will be collected , they will be assessed according to their cause and level of severity (Clavien-Dindo Classification). Infectious and metabolic complications, side effects of immunosuppression including renal function, New Onset Diabetes After Transplantation (NODAT), infection, incidence of post-transplant malignancy will be collected throughout the study from blood tests and ECBU. Acute organ rejection evaluation will be evaluated by allograft biopsy (lymphocytic infiltrate, apoptosis, artery endothelialitis)
Qualitive evaluationPreoperatively, 6 months, 12 months and 24 monthsSemi-structured patient interviews will be performed. The preoperative interview will investigate the functional aspects of urination and sexuality when suffering from penile defect. A specific interest will be given to the expectations of the patient and foreseen benefit of PT. The appropriation and the experience of allotransplantation will be explored along with the different functionnal domains.
Health-economic evaluation24 monthsThe cost per penile transplantation procedure including transplant preparation will be estimated from the hospital perspective. Moreover the quantity of resources consumed and the total penile transplantation cost per patient including post-transplantation cost follow-up cost will be assessed from the health care system perspective.

Countries

France

Contacts

Primary ContactPaul Neuville, Doctor
paul.neuville@chu-lyon.fr+33 4 72 67 88 37
Backup ContactLionel Badet, Professor
lionel.badet@chu-lyon.fr+33 4 72 11 11 40

Outcome results

None listed

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