Actively Recruiting
Incidence of Diaphragmatic Dysfunction After Non-Intubated Video-Assisted Thoracoscopic Surgery
Led by GCS Ramsay Santé pour l'Enseignement et la Recherche · Updated on 2026-01-14
120
Participants Needed
1
Research Sites
111 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Incidence of Diaphragmatic Dysfunction After Non-Intubated Video-Assisted Thoracoscopic Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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 will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hôpital Privé Claude Galien
Quincy-sous-Sénart, France, 91480
Actively Recruiting
Research Team
N
Nabil ZANOUN, MD
CONTACT
K
Karim GUESSOUS, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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