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NCT04325269

Continuous Ambulatory ECG Monitoring for Detection of Postoperative Atrial Fibrillation Following Thoracic Surgery

Status unknown Last updated 3 April 2020
What this trial tests

trial in Lung Cancer in 100 participants. Status unknown.

Timeline
1 April 2020
Primary endpoint
1 February 2021
1 June 2021

Quick facts

Lead sponsorUniversity of Manitoba
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment100
Start date1 April 2020
Primary completion1 February 2021
Estimated completion1 June 2021
Sites1 location across Canada

Conditions studied

Sponsor

University of Manitoba

Who can join

55 and older, any sex, with Lung Cancer or Atrial Fibrillation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Atrial fibrillation (AF) is a common and serious complication after lung resection. The incidence is likely underestimated, and risk may persist after leaving hospital. Recent development of simple wearable patch ECG devices may provide sensitive detection of AF in the extended postoperative period. Specific biomarkers may allow us to predict which patients are at risk of developing postoperative AF.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Lung Cancer

Currently open trials in the same condition.

Other University of Manitoba trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT04325269.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing