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Clinical Trials in France / NCT05912764
Recruiting Not applicable

Evaluation of Early Home Return in Patients With Enucleation of Prostate Adenoma

NCT05912764 · tracked via the Priya Life Science France tracker
Sponsor
GCS Ramsay Santé pour l'Enseignement et la Recherche
Phase
Not applicable
Started
2024-01-26
Last updated
2025-11-24

Condition(s) studied

Adenoma

Investigational drug(s) / intervention(s)

Patient support

Patient support: Patients will be supported by nurses before and after intervention and hospital leave

Study summary

Prostate adenoma management includes, if necessary, surgical treatments: resection or vaporization by endoscopy or by open surgery in case of a very large prostate. Laser technology is a curative treatment for prostate adenoma. The minimum duration of hospitalization, in the context of enucleation prostatic endoscopy by laser, is estimated at 48 hours.

The Union Clinique has developed an improved rehabilitation care pathway reducing hospitalization duration to 24 hours (one night hospitalization). This care pathway involves patient as an actor in its care but also health professionals, in particular nurses.

This study is based on the hypothesis that the model developed by the Union Clinique can be translated to other healthcare establishments and that home return supervized by nurses allows reducing hospital stay length without increasing the risk of serious complications for patients

Eligibility

Sex
MALE
Min age
45 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient planned for endoscopic enucleation of prostate adenoma with laser * Patient with symptomatic benign prostatic hyperplasia and refractory to medical reatment and/or * Patient with benign prostatic hyperplasia complicated by chronic retention of urine and/or * Patient with benign prostatic hyperplasia complicated by prostatitis and/or * Patient with symptomatic benign prostatic hyperplasia Exclusion Criteria: * Patient living beyond the scope of care by the nurses coordination * Bedridden patient or WHO clinical condition \>2 * Patient requiring curative anticoagulation which cannot be interrupted or relayed at home by heparin * Patient with double anti-platelet aggregation who cannot be interrupted

Primary outcome measure(s)

  • Re-hospitalizations and/or hospitalization extensions rate — 2 weeks
    the percentage of re-hospitalizations and/or hospitalization extensions

Trial sites (1)

FacilityCityRegionStatus
Clinique de l'Union Saint-Jean France Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05912764 on ClinicalTrials.gov ↗ ← All trials in France