Skip to content

A prospective, randomised controlled multi-centre trial comparing in-hospital treatment and early assisted discharge for exacerbations of Chronic Obstructive Pulmonary Disease (COPD).

A prospective, randomised controlled multi-centre trial comparing in-hospital treatment and early assisted discharge for exacerbations of Chronic Obstructive Pulmonary Disease (COPD).

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON23731
Enrollment
235
Registered
2007-11-12
Start date
2007-11-26
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Chronic Obstructive Pulmonary Disease (COPD), exacerbation treatment, early assisted discharge, cost-effectiveness. patient preference.

Interventions

Intervention group will be early assisted discharged home on the fourth day of hospitalisation. They will receive the same medical treatment as the control group, but in their own environment. The i

Sponsors

University Maastricht (UM), CAPHRI institute iMTA, Erasmus MC Rotterdam
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age 40 and older; 2. Competent; 3. COPD defined as minimally GOLD I and 10 PY; 4. Moderate to severe exacerbation.

Exclusion criteria

Exclusion criteria: 1. Major uncontrolled co-morbidity; 2. Mental disability; 3. Active alcoholism and/or drug abuse; 4. Inability to understand the program; 5. Living outside the region of care of the home care organisation; 6. Indication for ICU admission or NIPPV; 7. Insufficient direct caregiver.

Design outcomes

Secondary

MeasureTime frame
Secondary outcomes are: 1. Number of treatment failures; 2. Health care consumption/health care costs; 3. 3-month clinical control (CCQ EQ-5D); 4. 3-month re-admission rate; 5. 3 month mortality rate; 6. Patient and direct caregiver's satisfaction also a DCE will be performed to study which treatment characteristics influence patients' and cargivers' preferences for home or hospital treatment.

Primary

MeasureTime frame
Primary outcome is the CCQ score measured on day 7, representing changes in health condition.

Contacts

Public ContactCecile Utens

Catharina-ziekenhuis Eindhoven postbus 1350

cecile.utens@hag.unimaas.nl0031 (0)40-239 8779

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)