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Prospective Study of Persistent Dyspnea in Recovered COVID-19 Patients

Prospective Study of Persistent Dyspnea in Recovered COVID-19 Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04689490
Acronym
DISCOVID19
Enrollment
70
Registered
2020-12-30
Start date
2020-08-01
Completion date
2020-12-31
Last updated
2021-10-25

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

Conditions

Covid19, Dyspnea

Keywords

Dyspnea, Covid19, Cardiopulmonary exercise test

Brief summary

We conducted a national, single center (Hospital Clínico Universitario de Valladolid, Spain, Valladolid), prospective study of patients with prior hospitalization because of COVID-19 who were admitted between March 1st, 2020, and May 15th, 2020. All eligible patients underwent at least at first-time follow-up from the index event. Exclusion criteria were age \< 18 years old, pregnant women, terminally ill patients, active SARS-CoV-2 infections, inability to exercise and previous known severe pulmonary or heart disease. Patients underwent a clinical assessment for symptom burden, questionnaire for quality of life (Kansas City Cardiomyopathy Questionnaire and SF-36), venous blood sampling, 6-minute walking test (6-MWT), tests of lung function (spirometry and diffusing capacity of the lungs for carbon monoxide) and treadmill cardio-pulmonary exercise testing (CPET). 48-hours before the test of lung function and the CPET, all patients yielded a negative result in the reverse transcription-polymerase chain reaction (RT-PCR) for SARS-CoV-2. For definitive analysis patients were assigned to the control group if they did not refer dyspnea at the time of the follow-up, a small asymptomatic out-patient control group without prior hospitalization was also included.

Interventions

DIAGNOSTIC_TESTCardiopulmonary exercise test

Only diagnostic tests

Sponsors

Hospital Clínico Universitario de Valladolid
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Signed Informed Consent * Previous COVID-19 hospitalization with successful discharged * Availability of at least one follow up per clinical protocol

Exclusion criteria

* pregnant women * terminally ill patients * active SARS-CoV-2 infections * inability to exercise * previous known severe pulmonary or heart disease

Design outcomes

Primary

MeasureTime frameDescription
Aerobic capacity6 monthsMeasured as peak oxygen uptake
Total Lung Capacity (TLC)6 monthsPulmonary function test
Force Expiratory Volume in 1 second (FEV1)6 monthsPulmonary function test
Difussing Lung Capacity of CO (DLCO)6 monthsPulmonary function test
Forced Vital Capacity (FVC)6 monthsPulmonary function test
Left Ventricular (LV) Function6 monthsLeft Ventricular (LV) Function (Ecocardiagraphy-measured Cardiac Function)
Right Ventricular (RV) Function6 monthsRight Ventricular (RV) Function (Ecocardiagraphy-measured Cardiac Function)

Secondary

MeasureTime frameDescription
interleukine-66 monthsInflammatory and Cardiac Marker
Short Form 36 Health Survey (SF-36)6 monthsQuality of Life test
C reactive protein (CRP)6 monthsInflammatory and Cardiac Marker
Kansas City Cardiomyopathy Questionnaire (KCCQ)6 MonthsQuality of Life test
6 Minute Walk Test6 monthsWalking capacity
N-terminal pro hormone B-type natriuretic peptide (NT-proBNP)6 monthsInflammatory and Cardiac Marker
Troponin-T6 monthsInflammatory and Cardiac Marker
Ferritin6 monthsInflammatory and Cardiac Marker
D-Dimer6 monthsInflammatory and Cardiac Marker

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026