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Outpatient Hospitalization of Unaccompanied Patients at Home for Endovascular Treatment of Peripheral Arterial Disease. (ABALONE)

Primary Purpose

Peripheral Arterial Disease

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
24 months of inclusion of unaccompanied patients
18 months of inclusion of unaccompanied patients
12 months of inclusion of unaccompanied patients
6 months of inclusion of unaccompanied patients
Sponsored by
Fondation Hôpital Saint-Joseph
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Peripheral Arterial Disease focused on measuring ambulatory, accompanied patient, unaccompanied patient

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: 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) Exclusion Criteria: - Disorders of hemostasis Acute ischemia of the lower limbs Patient already included in ABALONE (2nd inclusion impossible) Patient already included in a type 1 interventional research protocol Patient under guardianship or curatorship Patient deprived of liberty Patient under legal protection

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Experimental

    Experimental

    Experimental

    Experimental

    Arm Label

    Experimental: Group1

    Experimental: Group2

    Experimental: Group3

    Experimental: Group4

    Arm Description

    In group 1: 5 centers will be randomized for the inclusion of unaccompanied patients for 24 months

    In group 2: 5 other centers will be randomized for the inclusion of unaccompanied patients for 18 months

    In group 3: 5 other centers will be randomized for the inclusion of unaccompanied patients for 12 months

    In group 4: 5 other centers will be randomized for the inclusion of unaccompanied patients for 6 months

    Outcomes

    Primary Outcome Measures

    Outpatient Hospitalization Rate for Endovascular Treatment of PAD at the End of the Procedure Period

    Secondary Outcome Measures

    Number of postoperative complications requiring re-hospitalization
    Functional improvement at 1 month as assessed by the Rutherford classification
    Assessment of patient anxiety using the HAS anxiety questionnaire
    Assessment of patient anxiety using the HAS anxiety questionnaire
    Assessment of patient anxiety using the HAS anxiety questionnaire

    Full Information

    First Posted
    January 20, 2023
    Last Updated
    March 3, 2023
    Sponsor
    Fondation Hôpital Saint-Joseph
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05756491
    Brief Title
    Outpatient Hospitalization of Unaccompanied Patients at Home for Endovascular Treatment of Peripheral Arterial Disease.
    Acronym
    ABALONE
    Official Title
    Outpatient Hospitalization of Unaccompanied Patients at Home for Endovascular Treatment of Peripheral Arterial Disease: a Cluster Randomized Trial.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    April 1, 2023 (Anticipated)
    Primary Completion Date
    April 1, 2026 (Anticipated)
    Study Completion Date
    April 1, 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Fondation Hôpital Saint-Joseph

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief 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.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Peripheral Arterial Disease
    Keywords
    ambulatory, accompanied patient, unaccompanied patient

    7. Study Design

    Primary Purpose
    Health Services Research
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    standard care: accompanied patients Remote surveillance: unaccompanied patients
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    2000 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Experimental: Group1
    Arm Type
    Experimental
    Arm Description
    In group 1: 5 centers will be randomized for the inclusion of unaccompanied patients for 24 months
    Arm Title
    Experimental: Group2
    Arm Type
    Experimental
    Arm Description
    In group 2: 5 other centers will be randomized for the inclusion of unaccompanied patients for 18 months
    Arm Title
    Experimental: Group3
    Arm Type
    Experimental
    Arm Description
    In group 3: 5 other centers will be randomized for the inclusion of unaccompanied patients for 12 months
    Arm Title
    Experimental: Group4
    Arm Type
    Experimental
    Arm Description
    In group 4: 5 other centers will be randomized for the inclusion of unaccompanied patients for 6 months
    Intervention Type
    Other
    Intervention Name(s)
    24 months of inclusion of unaccompanied patients
    Intervention Description
    inclusion for 6 months of accompanied patients in conventional outpatient care (observational period) and then inclusion for 24 months of unaccompanied with remonte surveillance patients and accompanied patients (interventional period)
    Intervention Type
    Other
    Intervention Name(s)
    18 months of inclusion of unaccompanied patients
    Intervention Description
    inclusion for 12 months of accompanied patients in conventional outpatient care (observational period) and then inclusion for 18 months of unaccompanied with remonte surveillance patients and accompanied patients (interventional period)
    Intervention Type
    Other
    Intervention Name(s)
    12 months of inclusion of unaccompanied patients
    Intervention Description
    inclusion for 18 months of accompanied patients in conventional outpatient care (observational period) and then inclusion for 12 months of unaccompanied with remonte surveillance patients and accompanied patients (interventional period)
    Intervention Type
    Other
    Intervention Name(s)
    6 months of inclusion of unaccompanied patients
    Intervention Description
    inclusion for 24 months of accompanied patients in conventional outpatient care (observational period) and then inclusion for 6 months of unaccompanied with remonte surveillance patients and accompanied patients (interventional period)
    Primary Outcome Measure Information:
    Title
    Outpatient Hospitalization Rate for Endovascular Treatment of PAD at the End of the Procedure Period
    Time Frame
    30 month
    Secondary Outcome Measure Information:
    Title
    Number of postoperative complications requiring re-hospitalization
    Time Frame
    1 month
    Title
    Functional improvement at 1 month as assessed by the Rutherford classification
    Time Frame
    1 month
    Title
    Assessment of patient anxiety using the HAS anxiety questionnaire
    Time Frame
    pre-procedure
    Title
    Assessment of patient anxiety using the HAS anxiety questionnaire
    Time Frame
    immediately after procedure
    Title
    Assessment of patient anxiety using the HAS anxiety questionnaire
    Time Frame
    Day 7

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: 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) Exclusion Criteria: - Disorders of hemostasis Acute ischemia of the lower limbs Patient already included in ABALONE (2nd inclusion impossible) Patient already included in a type 1 interventional research protocol Patient under guardianship or curatorship Patient deprived of liberty Patient under legal protection
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Yann GOUEFFIC
    Phone
    +33 (0)1 44 12 75 91
    Email
    ygoueffic@ghpsj.fr
    First Name & Middle Initial & Last Name or Official Title & Degree
    Florence LECERF
    Phone
    +33 (0) 1 40 94 25 17
    Email
    f.lecerf@ghpsj.fr

    12. IPD Sharing Statement

    Learn more about this trial

    Outpatient Hospitalization of Unaccompanied Patients at Home for Endovascular Treatment of Peripheral Arterial Disease.

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