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Study identifier: NCT06523140 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: RecruitingAUSTRAAL

Management of COPD Patients With BoraCare® Remote Monitoring Solution Including BVS3 Early Detection Score for COPD Exacerbations

Condition: COPD  ·  Sponsor: Biosency

PhaseNA
Planned participants380
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where10 locations

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The goal of this clinical trial is to demonstrate the superiority of remote monitoring with the Bora Care solution in patients with COPD and frequent exacerbations (experimental group) compared to conventional follow-up alone (control group) on the total number of hospital days per patient for respiratory deterioration over 12 months of follow-up. The main question it aims to answer is: Does remote monitoring of COPD patients reduce the average annual length of hospitalization for exacerbations of COPD patients? All participants will benefit a conventional clinical follow-up. Participants in experimental group will also benefit from the Bora care remote monitoring system.

This description comes directly from the study's public registry record.

Talk to the study team

Alexis TOULLEC  ·  02 21 65 70 01  ·  clinical@biosency.com

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Patient over 18 years of age with COPD defined according to the recommendations of the SPLF, whose level of respiratory function in a stable state is known (measured less than 12 months), recruited in pulmonology * Patient who has been hospitalized for COPD exacerbation in the previous 12 months * Informed patient who has signed consent, * Patient enrolled in a social security scheme (Art L1121-11 of the CSP) Exclusion Criteria: * Presence of a comorbidity considered unstable or very severe by the investigator. * Patient with psychological frailties, * Patient already included in another interventional trial, * Patient who does not speak French and is unable to use the Bora Band tool and without access to a caregiver, * Patient protected under guardianship or unable to give free and informed consent. * Pregnant or nursing woman

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (10)

CHU de BrestBrest, Brittany Region, FranceRecruiting
Centre Hospitalier Bretagne AtlantiqueVannes, Brittany Region, FranceRecruiting
Centre Hospitalier de ChartresLe Coudray, Centre-Val de Loire, FranceNot Yet Recruiting
Centre Hospitalier VerdunVerdun, Grand Est, FranceNot Yet Recruiting
Groupement des Hôpitaux de l'Institut Catholique de Lille (GHICL)Lille, Hauts-de-France, FranceNot Yet Recruiting
Clinique du MillénaireMontpellier, Occitanie, FranceNot Yet Recruiting
Centre Hospitalier Universitaire de ToulouseToulouse, Occitanie, FranceNot Yet Recruiting
Hôpital Européen MarseilleMarseille, Provence-Alpes-Côte d'Azur Region, FranceNot Yet Recruiting
Hôpital de la Pitié Salpêtrière - AP-HPParis, Île-de-France Region, FranceNot Yet Recruiting
Hôpital Cochin - AP-HPParis, Île-de-France Region, FranceRecruiting

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

BrestVannesLe CoudrayVerdun

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