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Not yet recruiting NCT07050030

Association of Preoperative Coronary Calcium Score and Postoperative Atrial Arrythmia in Patients Undergoing Robot-assisted Esophagectomy: Prospective Observational Study

— Observational Patients Undergoing Robot-assisted Esophagectomy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Patients Undergoing Robot-assisted Esophagectomy. Basic parameters: from 20 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
South Korea
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

This study aimed to evaluate the relationship between coronary artery calcium score measured before surgery and the incidence of atrial fibrillation after robot-assisted esophagectomy.

Primary outcome measures

  • Incidence of postoperative atrial fibrillation [Time frame: within 30 days postoperatively]

Eligibility criteria

Inclusion criteria

  • Patients aged 20 years or older undergoing robotic esophagectomy
  • Patients who underwent preoperative coronary computed tomography (CT) with a valid coronary artery calcium score

Exclusion criteria

  • emergency surgery
  • patients who cannot read consent forms(e.g., illiterate, foreigner, etc.)
  • patients with cognitive dysfunction
  • pregnant, lactating women
  • history of atrial fibrillation prior to surgery

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

South Korea · 1 center
  • Department of Anesthesiology and Pain Medicine, Anesthesia and Pain Research Institue, Yon — Seoul

Identifiers

NCT: NCT07050030 · 4-2025-0388

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗