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Respiratory Variability and Postoperative Complications During Thoracic Lung Resection.

Study acronym: RESPIVARIA
StatusRecruiting
PhaseNot applicable
Started
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Record status
This record was last updated August 20, 2026 (before its estimated September 30, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Trial status: Not Yet Recruiting to Recruiting
    • Primary and study completion dates: Oct 30, 2025 to Sep 30, 2026
    • Start date changed from estimate of Jul 1, 2024 to Oct 28, 2024
    • Study sites: 0 to 1
    v4
  2. Start date: Mar 1, 2024 to Jul 1, 2024
    • Primary and study completion dates: Jun 30, 2025 to Oct 30, 2025
    v3
  3. Start date: Dec 1, 2023 to Mar 1, 2024v2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Postoperative respiratory complications (PRC) represent a major public health issue. Majority of PRCs occur once the patient leaves the post-interventional monitoring room. Identifying patients at risk for PRC is therefore an important step for improving their post-operative care. In this context, any clinical marker making it possible to detect early alteration of the respiratory state in the postoperative phase deserves to be evaluated. This study is based on the hypothesis that measuring indices of respiratory variability which is synonymous with "good respiratory health" can be part of these markers. The measurement of respiratory variability will be done in patients with thoracic lung resection surgery before anesthetic induction and in the postoperative phase after extubation. It will be measured using a belt equipped with an external sensor allowing automatic and continuous analysis of thoracic movement by frequency analysis
Trial Details
NCT Number NCT06133777
Lead Sponsor GCS Ramsay Santé pour l'Enseignement et la Recherche
Conditions
(from sponsor)		 Lung Injury
Related terms Lung Injury
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov