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Feasibility of Suprapubic Transvesical Endoscopic Prostatectomy

B

Beni-Suef University

Status

Active, not recruiting

Conditions

Prostate

Treatments

Other: Suprapubic transvesical endoscopic prostatectomy

Study type

Interventional

Funder types

Other

Identifiers

NCT07327424
FMBSUREC/01072025/Mohamed

Details and patient eligibility

About

In patients with penile prosthesis, any transurethral procedure could place the implant at risk. The use of long or extra-long resectoscope can be of some assistance; however, these are not available in many institutions. So suprapubic transvesical endoscopic prostatectomy is newly developed to bypass the anterior urethra. Thus, the aim of this study is to determine safety and efficacy of Suprapubic Transvesical endoscopic prostatectomy.

Enrollment

80 estimated patients

Sex

Male

Ages

55+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male patients with moderate to severe lower urinary tract symptoms ( IPSS score ≥ 8 ) indicated for surgical intervention with prostate size less than 120 cc.

Exclusion criteria

  • History of previous pelvic surgery, urothelial cancer, kidney transplantation, uncontrolled coagulopathy, and significant central fat accumulation that could potentially increase the risk during transvesical access(body mass index not exceeding 27 kg/m2)

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

80 participants in 1 patient group

Suprapubic Transvesical endoscopic prostatectomy
Experimental group
Treatment:
Other: Suprapubic transvesical endoscopic prostatectomy

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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