Last updated: March 15, 2024
Sponsor: Assistance Publique Hopitaux De Marseille
Overall Status: Active - Recruiting
Phase
2
Condition
Peyronie's Disease
Enuresis
Urethral Strictures
Treatment
lipoaspiration
autologous ADSVF administration
urethrotomy
Clinical Study ID
NCT05857371
RCAPHM18_0020_1
2022-002175-11
Ages 18-85 Male
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Signed informed consent
- Male, aged from 18 to 85 years
- Bulbar urethral stenosis ≤ 3 cm.
- At least one urethral dilatation or urethrotomy for the bulbar stenosis in the past 24months before diagnosis of stenosis
- Ability to avoid corticoids or immunosuppressive drugs one month after treatment. Forany patients with either corticoid or immunosuppressive treatment the physician incharge of this treatment will be contacted and asked to give a written approval forone month cessation of the therapy
- Good general health status according to clinical history and a physical examination
- BMI > 18 to insure adequate access to abdominal or other subcutaneous adipose tissuefor adipose tissue harvesting
Exclusion
Exclusion Criteria:
- Urethral stenosis of other location than bulbar
- Urethral stenosis length > 3 cm
- Urethral stenosis on reconstructed penis (transgender, post amputation)
- Prior perineal or pelvic radiotherapy
- Concurrent urinary tract infection without treatment
- Concurrent perineal infection
- Penile cancer < 5 years
- Current or recent history of abnormal, severe, progressive, uncontrolled infectious,hepatic, haematological, gastrointestinal (except CD), endocrine, pulmonary, cardiac,neurological, psychiatric, or cerebral disease
- Congenital or acquired immunodeficiencies
- Contraindication to the anaesthetic or surgical procedure
- Corticoids or immunosuppressive drugs > 3 months
- Any active viral infection among the following: HIV, HTLV I and II, VHB, VHC andsyphillis
- Administrative restricted rights
- Presence of signs of obstructive voiding symptoms not directly attributable to thestricture at the discretion of the physician
- Diagnosis of untreated and unresolved BPH benign prostatic hyperplasia or BNC bladderneck contracture
- Diagnosis of carcinoma of the urethra, bladder or prostate within the last two (2)years
Study Design
Total Participants: 20
Treatment Group(s): 3
Primary Treatment: lipoaspiration
Phase: 2
Study Start date:
March 13, 2024
Estimated Completion Date:
April 30, 2028
Study Description
Connect with a study center
Assistance Publique Hopitaux de Marseille
Marseille,
FranceActive - Recruiting
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