Outpatient Hospitalization of Unaccompanied Patients at Home for Endovascular Treatment of Peripheral Arterial Disease: a Cluster Randomized Trial.

Status: Recruiting
Location: See all (20) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

In Westernized countries, the prevalence of peripheral arterial disease (PAD) is estimated at 15-20% of subjects over 70 years of age and is increasing considerably because of the aging of the population and the increasing prevalence of diabetes and renal insufficiency. In response to this increase in incidence, vascular surgeons must develop innovative treatments that minimize the use of resources in a context of budgetary constraints, in patients who are increasingly well informed, while maintaining the safety and effectiveness of the procedures performed. The endovascular technique has several advantages. First, it is a minimally invasive treatment, most often performed under local anesthesia. Secondly, the duration of the procedure and the length of hospitalization are reduced. In addition, the peri-operative morbidity and mortality is extremely low. In France, for many years, public health policies have encouraged the development of outpatient hospitalization. Endovascular treatment allows the development of outpatient care. The French Society of Vascular and Endovascular Surgery (SCVE) was the first European society to publish recommendations concerning the outpatient management of endovascular treatment of PAD. These recommendations aim to promote the development of outpatient treatment by providing a framework for practitioners wishing to offer this type of management. Concerning the patient and according to the SCVE recommendations, all types of occlusive arterial lesions of the lower limbs can be managed on an outpatient basis and only patients with severe comorbidities are excluded from this type of hospitalization. In addition, various studies have shown the safety of outpatient hospitalization for PAD. The absence of an accompanying person on the night following the procedure is considered an exclusion criterion for outpatient care. The objective of this Stepped-wedge Cluster Randomized Controlled Trial is to increase the use of outpatient hospitalization for endovascular treatment of PAD by proposing a care pathway adapted to people without an accompanying person on the night of the procedure at home.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• For all patients, the inclusion criteria are:

• Patient with symptomatic PAD (Rutherford 1-5) requiring endovascular revascularization that can be performed on an outpatient basis

• Procedure listed in the Common Classification of Medical Procedures

• Patient with a good understanding of the constraints of the study

• Patient with an ASA score of 1 to 3 (stable)

• Patient registered with the social security system

• Patient living less than 1 hour by car from the care facility or from a care facility able to care for this type of patient

• Patient willing to remain hospitalized if necessary

⁃ For accompanied patients only:

⁃ \- Patient does not object to the processing of his or her data

⁃ Only for isolated patients:

• Patient with free, informed and written consent

• Patient agreeing to wear the remote monitoring device at discharge from the outpatient revascularization hospitalization

• Patient agreeing to the processing of his or her personal data with the remote monitoring provider

• Patient not living in an area not served by a cell phone network (white zone)

Locations
Other Locations
France
Chu Jean Minjoz
RECRUITING
Besançon
Centre Hospitalier de Béziers,
RECRUITING
Béziers
Hopital Universitaire Ambroise Paré,
RECRUITING
Boulogne-billancourt
CHRU Cavale Blanche
RECRUITING
Brest
Chu Cote de Nacre
RECRUITING
Caen
Hôpital Universitaire Gabriel Montpied
RECRUITING
Clermont-ferrand
Pôle médical du Grand large,
RECRUITING
Décines-charpieu
Hopital Le Bocage,
RECRUITING
Dijon
Hopital Prive Dijon Bourgogne
RECRUITING
Dijon
Clinique Mutualiste Porte de L'Orient
RECRUITING
Lorient
Chu de Nantes
RECRUITING
Nantes
Hopital Prive Du Confluent
RECRUITING
Nantes
Chu de Nice,
RECRUITING
Nice
Hôpital Saint Joseph
RECRUITING
Paris
Polyclinique Francheville,
RECRUITING
Périgueux
Clinique de L'Europe
RECRUITING
Rouen
Centre Hospitalier Yves Le Foll-
RECRUITING
Saint-brieuc
Centre Hospitalier Privé SAINT GREGOIRE
RECRUITING
Saint-grégoire
Clinique Esquirol-Saint-Hilaire,
RECRUITING
Saint-hilaire
Médipôle Lyon Villeurbanne,
RECRUITING
Villeurbanne
Contact Information
Primary
Yann GOUEFFIC
ygoueffic@ghpsj.fr
+33 (0)1 44 12 75 91
Backup
Florence LECERF
f.lecerf@ghpsj.fr
+33 (0) 1 40 94 25 17
Time Frame
Start Date: 2023-04-11
Estimated Completion Date: 2026-04-11
Participants
Target number of participants: 2000
Treatments
Experimental: Experimental: Group1
In group 1: 5 centers will be randomized for the inclusion of unaccompanied patients for 24 months
Experimental: Experimental: Group2
In group 2: 5 other centers will be randomized for the inclusion of unaccompanied patients for 18 months
Experimental: Experimental: Group3
In group 3: 5 other centers will be randomized for the inclusion of unaccompanied patients for 12 months
Experimental: Experimental: Group4
In group 4: 5 other centers will be randomized for the inclusion of unaccompanied patients for 6 months
Sponsors
Leads: Fondation Hôpital Saint-Joseph

This content was sourced from clinicaltrials.gov