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Clinical Trials in France / NCT06486168
Recruiting Not applicable

Incidence of Diaphragmatic Dysfunction After Non-Intubated Video-Assisted Thoracoscopic Surgery

NCT06486168 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2024-12-10
Last updated
2026-01-14

Condition(s) studied

Diaphragmatic Dysfunction

Investigational drug(s) / intervention(s)

NIVATS

NIVATS: Non-Intubated Video-Assisted Thoracic Surgery (NIVATS) is the least invasive approach available. It is part of an optimal Enhanced Recovery After Surgery (ERAS) pathway and allows for expanding surgical indications in patients with poor cardio-pulmonary function.

Study summary

The objective of this this single-center prospective longitudinal study is to evaluate the incidence of diaphragmatic dysfunction after non-intubated video-assisted thoracoscopic surgery (NIVATS).

Participant will be evaluated during surgery, 2 hours and 24 hours after surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient aged 18 years or older * Patient who has read and signed the informed consent form for participation in the study * Patient undergoing surgery with video-assisted thoracoscopic surgery without intubation Exclusion Criteria: * Known or detected diaphragmatic dysfunction before the intervention * Patient not affiliated with the French social security system * Patient under legal protection, guardianship, or curatorship * Patient already enrolled in another therapeutic study protocol (involving medications or non-drug therapies) * Patient in an exclusion period from a previous clinical study * Mental deficiency or any other reason that may hinder understanding or strict adherence to the protocol

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hôpital Privé Claude Galien Quincy-sous-Sénart France Recruiting

More GCS Ramsay Santé pour l'Enseignement et la Recherche trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06486168 on ClinicalTrials.gov ↗ ← All trials in France