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Efficacy of Telemetry-assisted Care in Home Home Vented COPD

NCT05287555 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 54

Last updated 2025-12-02

No results posted yet for this study

Summary

This study in patients suffering of Chronic Obstructive Pulmonary disease (COPD) aims to investigate whether telemonitoring of their non invasive ventilation (NIV) device together with targeted, tailored intervention in case of increasing symptoms or ventilation abnormalities improves the therapy adherence and effectiveness and can reduce the need for hospitalizations.

Conditions

Interventions

OTHER

Standard Care

NIV, Supplies as needed, especially masks, tubes, humidifiers, and modems

OTHER

Telemonitoring Care

NIV, Supplies as needed, especially masks, tubes, humidifiers, SpO2 sensor and modems.

Sponsors & Collaborators

  • Heinen und Löwenstein GmbH & Co. KG

    collaborator INDUSTRY

  • Georg Nilius, Prof DR med

    lead INDUSTRY

Principal Investigators

  • Gearg Nilius, MD · KEM | Evang. Kliniken Essen-Mitte gGmbH

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-04-25
Primary Completion
2025-04-15
Completion
2025-11-24

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05287555 on ClinicalTrials.gov