Medico-economical Evaluation of Patient-hotel in Urology
NCT ID: NCT02890017
Last Updated: 2019-12-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
10 participants
INTERVENTIONAL
2017-07-28
2019-01-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The aim is to show that those two strategies are not different in term of adverse effects or rehospitalization, and that the patient-hotel provide a better quality of life at a reduced cost, in order to generate savings for the paying agent: the Healthcare insurance.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Hotel-Ambu
Outpatient surgery with a patient-hotel night
postoperative hotel
Outpatient surgery First night stay in a defined patient-hotel Patient come for consultation the next morning of surgery to remove the catheter and/or the compressive bandage. The absence of adverse events is checked, the discharge is confirmed and the evaluation questionnaire is given to the patient.
Postoperative consultation at 1 and 3 months.
conventional hospitalization
conventional hospitalization
conventional hospitalization
Hospitalization for surgery and first postoperative night stay. Postoperative consultation at 1 and 3 months
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
postoperative hotel
Outpatient surgery First night stay in a defined patient-hotel Patient come for consultation the next morning of surgery to remove the catheter and/or the compressive bandage. The absence of adverse events is checked, the discharge is confirmed and the evaluation questionnaire is given to the patient.
Postoperative consultation at 1 and 3 months.
conventional hospitalization
Hospitalization for surgery and first postoperative night stay. Postoperative consultation at 1 and 3 months
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Healthcare insurance affiliation
* Surgeries : sacral nerve neurostimulation, urinary artificial sphincter, or prosthetic penile implant
* ASA (American Society of Anesthesiology) score between I and III
* Patients that can be accompanied by a person with a car
* Prior Informed Consent procedure form signed
* Hospitalisation in Lyon Sud Hospital
Exclusion Criteria
* Inability to understand the procedure
* History of cognitive or psychiatric disorders
* Non eligibility to out patient
* Pregnant or breastfeeding patients
* No affiliation to Healthcare insurance
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Hospices Civils de Lyon
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Service d'Urologie du Centre Hospitalier Lyon Sud, Hospices Civils de Lyon
Pierre-Bénite, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
69HCl15_ 0513
Identifier Type: -
Identifier Source: org_study_id