Actively Recruiting

Phase Not Applicable
Age: 40Years +
MALE
NCT05574244

Comparison of Functional Outcomes of Ejaculation-preserving Partial Trans Urethral Resection of the Prostate With Complete Trans Urethral Resection of the Prostate for Benign Prostatic Obstruction

Led by University Hospital, Bordeaux · Updated on 2026-04-09

336

Participants Needed

17

Research Sites

339 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

It has been demonstrated that sexual activity was common in the majority of men over 50 years old and was an important component of overall quality of life (QoL). Ejaculatory dysfunction (EjD) is the most common side effect of surgical treatment of benign prostatic obstruction (BPO). It has been considered for decades to be an inevitable consequence of restoring micturition comfort. EjD can have a substantial deleterious effect on the QoL of men with previously maintained regular sexual activity, inducing decreased orgasmic intensity and increased levels of anxiety and depression. A better understanding of the physiology of ejaculation has enabled the emergence of modified surgical techniques that aim to preserve antegrade ejaculation. Our hypothesis is that conservation of ejaculation can be achieved by modified surgical procedures without compromising functional outcomes.

CONDITIONS

Official Title

Comparison of Functional Outcomes of Ejaculation-preserving Partial Trans Urethral Resection of the Prostate With Complete Trans Urethral Resection of the Prostate for Benign Prostatic Obstruction

Who Can Participate

Age: 40Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Man over 40 years old
  • Indication for surgical treatment of benign prostatic hyperplasia
  • Prostate volume between 30 cc and 150 cc as assessed by ultrasound or MRI
  • International Prostatic Symptom Score (IPSS) of 12 or higher
  • Maximum urinary flow rate (Qmax) of 15 ml/s or less
  • Affiliated with the French national social security system
  • Willing and able to comply with scheduled visits
  • Able to provide informed consent
  • Signed informed consent form
Not Eligible

You will not qualify if you...

  • Unwilling to accept the treatment
  • No pre-operative ejaculation or sexual activity
  • Neurological disorders causing urinary problems
  • History of prostate surgery
  • Symptomatic urethral stricture
  • History of prostate cancer
  • History of radiotherapy or pelvic surgery
  • Refusal of partial surgery
  • Life expectancy less than 3 years
  • Unable to understand or voluntarily consent to the study or complete study tasks
  • Participation in another clinical trial involving investigational products within 1 month before study entry

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 17 locations

1

CH Pays d'Aix

Aix-en-Provence, France

Actively Recruiting

2

CHU Angers

Angers, France

Actively Recruiting

3

Centre Hospitalier Universitaire de Bordeaux

Bordeaux, France, 33000

Actively Recruiting

4

CHU Mondor

Créteil, France

Withdrawn

5

Hôpital Claude Huriez

Lille, France

Withdrawn

6

CHU de Limoges

Limoges, France

Actively Recruiting

7

Hôpital Nord Marseille

Marseille, France

Actively Recruiting

8

Polyclinique Saint George

Nice, France

Actively Recruiting

9

Hôpital cochin

Paris, France

Actively Recruiting

10

Hôpital Prive Francheville

Périgueux, France

Actively Recruiting

11

Hôpital Lyon Sud HCl Bât.3C Centre Hospitalier Lyon Sud

Pierre-Bénite, France

Actively Recruiting

12

Hôpital Privé des Côtes D'Armor

Plérin, France

Actively Recruiting

13

CHU de Reims- Hôpital Robert Debré

Rennes, France

Actively Recruiting

14

CHU de Rennes

Rennes, France

Actively Recruiting

15

Clinique Pasteur

Toulouse, France

Withdrawn

16

CHRU Hôpitaux de tours

Tours, France

Withdrawn

17

Hopital Privé de Versailles, Clinique des Franciscaines

Versailles, France

Actively Recruiting

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Research Team

G

Grégoire ROBERT

CONTACT

M

Méric BEN BOUJEMA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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Comparison of Functional Outcomes of Ejaculation-preserving Partial Trans Urethral Resection of the Prostate With Complete Trans Urethral Resection of the Prostate for Benign Prostatic Obstruction | DecenTrialz