Multisystem Shortness of Breath Evaluation Study

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03276507

Acronym

MUSE

Enrollment

Registered

2017-09-08

Start date

2016-11-01

Completion date

2018-06-01

Last updated

2017-11-09

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

Conditions

Dyspnea

Brief summary

The MUSE study is a prospective observational cohort study of patients referred to pulmonary and/or cardiology specialty clinic for evaluation of shortness of breath or dyspnea. Patients will undergo all pertinent testing and will be required to fill out a number of epidemiologic and quality of life related questionnaires. Follow up will continue for at least one year.

Interventions

DIAGNOSTIC_TESTPulmonary function studies

DIAGNOSTIC_TESTEchocardiogram

DIAGNOSTIC_TESTElectrocardiogram

DIAGNOSTIC_TESTChest radiography

DIAGNOSTIC_TESTBlood test

BEHAVIORALQuality of life questionnaire

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 90 Years

Healthy volunteers

Inclusion criteria

* Patients referred to Pulmonary and/or Cardiology clinic for the evaluation of unexplained dyspnea.

Exclusion criteria

* Patients with a known cause of dyspnea such as established cardiopulmonary disease

Design outcomes

Primary

Measure	Time frame	Description
Dyspnea etiology	3 months	All patients will undergo cardiopulmonary testing and will be offered quiestionnaires including the M3 online questionnaire

Secondary

Measure	Time frame	Description
Quality of Life	6 months	Several questionnaires will be used including the M3 questionnaire

Countries

Spain

Contacts

Primary ContactLuis M Seijo, MD

luis.seijo@fjd.es91 550 4800

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026