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CompletedNCT04749212Updated Mar 13, 2025

Perioperative Troponin I and NT Pro-BNP in Lung Resection

An observational study in Cardiac Ischemia, Thoracic Cancer and Complication,Postoperative, sponsored by Hospital Universitari Vall d'Hebron Research Institute. Completed at 1 site in Spain. Open to participants aged 45 Years and older. Per ClinicalTrials.gov, last updated 2025-03-13.

Sponsored by Hospital Universitari Vall d'Hebron Research Institute · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
475
Ages
45 Years and older
Sex
All
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Study summary

After lung resection, troponin elevation may be regulated by mechanisms other than myocardial ischemia. Perioperative natriuretic peptides measurement may help identify changes in ventricular function during thoracic surgery. Integrating both cardiac biomarkers may improve the predictive value for cardiovascular complications after lung resection.

Read the detailed description

Objectives: To evaluate the incidence and magnitude of perioperative N-terminal pro brain natriuretic peptide (NT-proBNP) and high-sensitivity troponin I (Tn I) elevation in patients undergoing pulmonary resection and its predictive value for cardiovascular complications. Methodology: Prospective, multicenter, observational cohort study in patients >45 years undergoing elective thoracic surgery for lung resection. Cardiac biomarkers Tn I and NT-proBNP will be measured preoperatively and at postoperative days 1 and 2. Risk score for major cardiovascular postoperative complications will be calculated depending of both biomarkers perioperative changes.

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Conditions studied

  • Cardiac Ischemia
  • Thoracic Cancer
  • Complication,Postoperative
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In context

Coronary Artery Disease

5,598 studies on the registry are indexed under Coronary Artery Disease; 955 are open to participants now.

This study's enrollment of 475 is above the median of 336 across 1,946 observational studies indexed under Coronary Artery Disease.

Browse Coronary Artery Disease studies →

Lead sponsor

Hospital Universitari Vall d'Hebron Research Institute is the lead sponsor of 268 studies on the registry; 61 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
45 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adulty patients undergoing elective thoracic and lung resection surgery: neumonectomy, lobectomy, bilobectomy or segmentectomy

Inclusion criteria

  • Age ≥45 years old
  • Patients undergoing elective surgery for lung resection

Exclusion criteria

Exclusion Criteria:

  • Patients undergoing urgent, emergent, or nonthoracic surgery
  • Patients or family did not consent to participate
  • Presence of symptoms related with infection or sepsis
  • Patients with a documented history of severe heart failure and/or ejection fraction lower than 30%
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
475 participants (actual)
Patient registry
No

Interventions

  • Diagnostic testserum high-sensitivity Troponin I (TnI) and NT-Pro-Brain Natriuretic Peptide (NT-proBNP)

    Both biomarkers will be determined in each patient preoperatively and at postoperative day 1 and day 2.Measurements will not necessarily be taken independently of other measurements, meaning that the addition of the biomarker could be included in routine pre or postoperative day-1 and day 2 blood tests.

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What researchers measure

Primary outcomes

  1. NT-proBNP perioperative changes

    Perioperative change in NT-Pro-Brain Natriuretic Peptide (NT-proBNP) levels in patients undergoing pulmonary resection. Cutt-of values will be NT-proBNP ≥ 300 pg/ml pg/ml

    Time frame: Change from baseline NT-proBNP at two-days after surgery

  2. TnI perioperative changes

    Perioperative changes in high-sensitivity troponin I (TnI) levels in patients undergoing pulmonary resection. Cutt-of values will be TnI ≥45 ng/L

    Time frame: Change from baseline TnI at two-days after surgery

  3. Major cardiovascular complications

    Postoperative non-fatal cardiac arrest, acute myocardial infarction, angina, congestive heart failure, new clinically relevant cardiac arrhythmia, cardiovascular death

    Time frame: 30-days after surgery

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Study locations

1 site
  • Hospital Universitari Vall d'Hebron
    Barcelona, Spain
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 13, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04749212
Lead sponsor
Hospital Universitari Vall d'Hebron Research Institute
Responsible party
Sponsor
First posted
Feb 11, 2021
Start date
May 19, 2021
Primary completion
Nov 30, 2023
Completion
Jan 31, 2025
Last update
Mar 13, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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