Cardiac complicAtions in Patients With SARS Corona vIrus 2 (COVID-19) regisTrY (CAPACITY-COVID)
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ClinicalTrials.gov Identifier: NCT04325412 |
Recruitment Status :
Recruiting
First Posted : March 27, 2020
Last Update Posted : November 10, 2020
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Condition or disease |
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COVID-19; Cardiovascular Diseases |
The aim of CAPACITY is to collect data regarding the cardiovascular history, diagnostic information and occurrence of cardiovascular complications in COVID-19 patients. By collecting this information in a standardized manner, CAPACITY can aid in providing more insight in (1) the incidence of cardiovascular complications in patients with COVID-19, and (2) the vulnerability and clinical course of COVID-19 in patients with an underlying cardiovascular disease.
The CAPACITY extension to the ISARIC-WHO CRF consists of additional data collection instruments for:
- cardiac history and cardiovascular risk factors
- prior use of cardiac medication or NSAIDs
- electrocardiography (ECG)
- echocardiography
- cardiac MRI
- invasive cardiac procedures
- cardiac complications
- cardiac biomarkers
- cardiac outcome during admission
Study Type : | Observational [Patient Registry] |
Estimated Enrollment : | 1000 participants |
Observational Model: | Cohort |
Time Perspective: | Prospective |
Target Follow-Up Duration: | 30 Days |
Official Title: | Cardiac complicAtions in Patients With SARS Corona vIrus 2 regisTrY |
Actual Study Start Date : | March 23, 2020 |
Estimated Primary Completion Date : | March 23, 2021 |
Estimated Study Completion Date : | June 23, 2021 |

- The incidence of cardiovascular complications in patients with COVID-19 [ Time Frame: 30 days ]

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Probability Sample |
Inclusion Criteria:
- Highly suspected/confirmed infection with SARS-CoV-2
Exclusion Criteria:
- Patients that opt-out

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04325412
Contact: Folkert W. Asselbergs, MD, PhD | +31 (0) 88 755 5555 | f.w.asselbergs@umcutrecht.nl |
Netherlands | |
University Medical Center Utrecht | Recruiting |
Utrecht, Netherlands, 3584 CX | |
Contact: Marijke Linschoten, MD +31 (0)88 755 5555 m.p.m.linschoten@umcutrecht.nl |
Responsible Party: | Prof. Dr. F.W. Asselbergs, UMC Utrecht |
ClinicalTrials.gov Identifier: | NCT04325412 |
Other Study ID Numbers: |
20-161/C |
First Posted: | March 27, 2020 Key Record Dates |
Last Update Posted: | November 10, 2020 |
Last Verified: | November 2020 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Undecided |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Coronavirus Infections Cardiovascular Diseases Coronaviridae Infections |
Nidovirales Infections RNA Virus Infections Virus Diseases |