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Wireless Assessment of Respiratory and Circulatory Distress in Chronic Obstructive Pulmonary Disease

Wireless Assessment of Respiratory and Circulatory Distress in Chronic Obstructive Pulmonary Disease - A Pilot Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03467815
Acronym
WARD-COPD
Enrollment
30
Registered
2018-03-16
Start date
2018-03-15
Completion date
2018-06-07
Last updated
2018-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease, Dyspnea

Keywords

Wireless monitoring, Continuous monitoring, Vital parameters, Clinical deterioration

Brief summary

For patients admitted to the medical ward, it is usually difficult to predict if their clinical condition will deteriorate, however subtle changes in vital signs are usually present 8 to 24 hours before a life-threatening event such as respiratory failure leading to ICU admission, or unanticipated cardiac arrest. Such adverse trends in clinical observations can be missed, misinterpreted or not appreciated as urgent. New continuous and wearable 24/7 clinical vital parameter monitoring systems offer a unique possibility to identify clinical deterioration before patients progress beyond the point-of-no-return, where adverse events are inevitable. The WARD-COPD project aims to determine the number and duration of cardiopulmonary micro events during the first 4 days after hospital admission with Acute Exacerbation of COPD. We will also test the server installation, develop a database of core data and assess the frequency of artefacts and failure to capture the continuous monitoring signal.

Interventions

None listed

Sponsors

Technical University of Denmark
CollaboratorOTHER
Rigshospitalet, Denmark
CollaboratorOTHER
Bispebjerg Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

Adult patients admitted to hospital for Acute Exacerbation of COPD (AECOPD). Investigators will review the electronic patient chart for a primary diagnosis of AECOPD.

Exclusion criteria

* Patient expected not to cooperate. * Patient allergic to plaster, plastic or silicone. * Active therapy withdrawn

Design outcomes

Primary

MeasureTime frameDescription
Blood oxygen saturation resulting in a single parameter score of 3 according to EWS algorithmThe patients are monitored for 4 daysHypoxemia: arterial oxygen saturation \< 92 %
Heart rate resulting in a single parameter score of 3 according to EWS algorithmThe patients are monitored for 4 daysAll data from the monitoring will be analyzed using the thresholds from the EWS algorithm and will be sorted into relevant categories. The following thresholds are used: Bradycardia: pulse \< 41 bpm Tachycardia: pulse \> 130 bpm
Respiratory rate resulting in a single parameter score of 3 according to EWS algorithmThe patients are monitored for 4 daysBradypnea: \< 9 breaths/min Tachypnea: \> 24 breaths/min
Blood pressure resulting in a single parameter score of 3 according to EWS algorithmThe patients are monitored for 4 daysHypotension: Systolic blood pressure \< 91 mmHg Hypertension: Systolic blood pressure \> 219 mmHg

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026