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CompletedNCT05060302SPECKLETHOUpdated Jun 11, 2026

Prognosis of Right Ventricular Dysfunction Assessed by Speckle Tracking in Postoperative Thoracic Surgery

An interventional study of transthoracic echocardiography (TTE) in Right Ventricle and Thoracic Surgery, sponsored by Centre Hospitalier Universitaire, Amiens. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-06-11.

Sponsored by Centre Hospitalier Universitaire, Amiens · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
191
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

In postoperative thoracic surgery (lobe resection, pneumonectomy or wedge resection), cardiovascular complications are the most frequent (10 to 15%) with a significant morbi-mortality rate. Right ventricular (RV) dysfunction is a complication that can be multifactorial in post thoracic surgery. The RV longitudinal shortening fraction (RV-LSF) is a new 2D-STE parameters able to more accurately detect patients with RV dysfunction compared to conventional echocardiographic parameters.

This project is a single-center, prospective, interventional study of patients hospitalized at the Amiens University Hospital for scheduled thoracic surgery. TTE is performed preoperatively, at day 2 and day 15 following the thoracic surgery. Echocardiographic parameters will be measured by an echocardiographic expert in offline with a dedicated software. MACE criteria will be collected at day 2, day 15 and day-30 following the thoracic surgery.

02

Conditions studied

  • Right Ventricle
  • Thoracic Surgery

Keywords

  • Right ventricle
  • speckle tracking
  • thoracic surgery
03

In context

Lead sponsor

Centre Hospitalier Universitaire, Amiens is the lead sponsor of 576 studies on the registry; 178 are open to participants now.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Adult patient (>18 years)
  • Patient hospitalized at the Amiens University Hospital for scheduled thoracic surgery (lobectomy, pneumonectomy, wedge resection).
  • Surgery by thoracotomy or video-assisted thoracic surgery
  • Information of the patient and collection of his non-opposition

Exclusion criteria

Exclusion Criteria:

  • Patient with poor echogenicity on TTE not allowing evaluation of 2D-STE or conventional parameters of the RV.
  • Patient with a rapid supraventricular rhythm disorder (HR > 100) at the time of TTE
  • Patient under mechanical ventilation
  • Patient under extracorporeal membrane oxygenation
  • Patients under guardianship or legal protection
  • Patients whose clinical condition does not allow for their non-opposition
  • Pregnant women
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
191 participants (actual)

Interventions

  • Othertransthoracic echocardiography (TTE)

    the included patients have a TTE preoperatively in order to evaluate the RV systolic function. TTE will also be done at day 2 and day-15 during the follow-up surgical consultation.

06

What researchers measure

Primary outcomes

  1. occurrence of a major cardiovascular event (MACE)

    MACE is a composite criteria. MACES criteria is defined as the occurrence of at least one of the following events: A cardiovascular death or a documented supraventricular tachycardia (atrial fibrillation and/or flutter) of duration \> 30 seconds or, an acute myocardial infarction or, an hospitalization for a right ventricular failure or, an hospitalization for a left ventricular failure.

    Time frame: day 30

Secondary outcomes

  1. Variation of RV systolic function from baseline in patients with MACE

    Time frame: at day 1

  2. Variation of RV systolic function from baseline in patients without MACE

    Time frame: at day 1

  3. Variation of RV systolic function from baseline in patients with MACE

    Time frame: at day 2

  4. Variation of RV systolic function from baseline in patients without MACE

    Time frame: at day 2

  5. Variation of RV systolic function from baseline in patients with MACE

    Time frame: at day 15

  6. Variation of RV systolic function from baseline in patients without MACE

    Time frame: at day 15

  7. Variation of RV systolic function from baseline in patients with MACE

    Time frame: within day 30

  8. Variation of RV systolic function from baseline in patients without MACE

    Time frame: within day 30

  9. Assessment of RV systolic function preoperatively

    Time frame: at day 30

  10. occurrence of a postoperative complication

    Time frame: at day 30

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Study locations

1 site
  • CHU Amiens Picardie
    Amiens, France
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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 Jun 11, 2026, 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
NCT05060302
Lead sponsor
Centre Hospitalier Universitaire, Amiens
Responsible party
Sponsor
First posted
Sep 29, 2021
Start date
Sep 13, 2021
Primary completion
Nov 8, 2023
Completion
Jan 7, 2025
Last update
Jun 11, 2026

Oversight

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

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This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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