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

Recruiting now · Not applicable

Conditions studied: Diaphragmatic Dysfunction

In brief

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.

Key facts

Study ID

NCT06486168

Run by

GCS Ramsay Santé pour l'Enseignement et la Recherche

People needed

120

Starts

2024-12-10

Expected to finish

2027-02-01

Last updated by the study team

2026-01-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• Hôpital Privé Claude Galien — Quincy-sous-Sénart, France (enrolling)

Full record on ClinicalTrials.gov

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