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NCT02622412: BreathEase
Evaluation of a Multi-professional Breathlessness Service for Patients With Breathlessness Due to Any Advanced Disease
NA trial testing Multi-professional breathlessness service (MBS) in Breathlessness in 183 participants. Completed in 30 April 2019.
1 February 2019
Quick facts
| Lead sponsor | Ludwig-Maximilians - University of Munich |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 183 |
| Start date | 2 March 2015 |
| Primary completion | 1 February 2019 |
| Estimated completion | 30 April 2019 |
| Sites | 1 location across Germany |
Drugs / interventions tested
- Multi-professional breathlessness service (MBS)
- Delayed MBS Intervention
Conditions studied
- Breathlessness — all drugs for Breathlessness →
- COPD — all drugs for COPD →
- Cancer — all drugs for Cancer →
- Chronic Heart Failure — all drugs for Chronic Heart Failure →
Sponsor
Ludwig-Maximilians - University of Munich
Who can join
18 and older, any sex, with Breathlessness or COPD. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Breathlessness is a common and distressing symptom in patients with advanced diseases like cancer, chronic obstructive pulmonary disease (COPD), chronic heart failure (CHF) or lung fibrosis, which broadly impacts on patients' quality of life and may result in high burden for carers. This single-blinded randomized controlled fast track trial evaluates the effectiveness of a multi-professional breathlessness service in patients with advanced and chronic diseases. The intervention group will get immediate access to the breathlessness service whereas the control group will receive standard care and get access to the service after a waiting time of eight weeks. Primary endpoints are mastery of breathlessness and quality of life, measured with the CRQ (Chronic Respiratory Questionnaire) as well as the reduction of symptom burden of patients and burden of carers. The evaluation of the cost effectiveness of the breathlessness service from the perspective of the German health system is a further study aim.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
BreathEase: rationale, design and recruitment of a randomised trial and embedded mixed-methods study of a multiprofessional breathlessness service in early palliative care.
Schunk M, Berger U, Le L, Rehfuess E, et al · · 2021 · cited 2× · PMID 34671668 · DOI 10.1183/23120541.00228-2020
Verify or expand the search:
- PubMed search for NCT02622412
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02622412 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Ludwig-Maximilians - University of Munich
- Last refreshed: 9 August 2019
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02622412.
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