Early home return for patients after prostate adenoma surgery
Official title: Evaluation of Early Home Return Care Pathway in Patients Who Have Undergone Endoscopic Enucleation of Prostate Adenoma by Laser
Run by GCS Ramsay Santé pour l'Enseignement et la Recherche · NCT05912764 · Data updated 2026-11-12
This study is testing a new way to help patients go home sooner after prostate surgery by providing supervised care at home to see if it keeps them safe and helps them recover better.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 45 Years and up |
| Sex | Men only |
| Enrollment | 440 (estimated) |
| Sponsor | GCS Ramsay Santé pour l'Enseignement et la Recherche Academic / other |
| Locations | 1 site (Saint-Jean) |
| Status | Recruiting |
| Started | January 26, 2024 |
| Main results expected | August 15, 2027 |
| Study ends | August 15, 2027 |
| Registry record updated | November 24, 2025 |
| Trial ID | NCT05912764 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include patients scheduled for endoscopic enucleation of prostate adenoma who have symptomatic benign prostatic hyperplasia and are refractory to medical treatment.
✕Probably not a fit
Patients who are bedridden, require continuous anticoagulation, or live outside the care coordination area will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates a new rehabilitation care pathway aimed at reducing the hospitalization duration for patients undergoing endoscopic enucleation of prostate adenoma using laser technology. Traditionally, patients are hospitalized for at least 48 hours, but this approach seeks to allow discharge within 24 hours while ensuring patient safety through supervised home care by nurses. The study hypothesizes that this model can be effectively implemented in other healthcare settings without increasing the risk of complications. The intervention focuses on improving patient involvement in their care and enhancing the overall recovery process.
Why it matters
Potential benefit: If successful, this approach could significantly reduce hospital stays for patients, leading to improved quality of life and reduced healthcare costs.
How similar studies have gone: While this specific approach is novel, similar studies have shown promise in reducing hospitalization times in other surgical contexts.
Who can join: the full rules
Show full inclusion / exclusion criteria
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
Where it's running
-
Clinique de l'Union
Saint-Jean, France Recruiting
Study contacts
- Principal investigator: Philippe ROUVELLAT, MD — Gcs Ramsay Sante
- Study coordinator: Philippe ROUVELLAT, MD
- Email: r.rouvellat.union@gmail.com
- Phone: + 33 5 61 37 82 93
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.