Thoracic Surgery Clinical Trial
— OFATOfficial title:
Evaluation of an "Opioid Free Anesthesia" Protocol in Thoracoscopic Carcinological Thoracic Surgery
NCT number | NCT05308355 |
Other study ID # | RC22_0112 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | April 4, 2022 |
Est. completion date | April 30, 2023 |
Verified date | September 2023 |
Source | Nantes University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Evaluation of a service OFA (Opioid-free Anesthesia) protocol on post-operative pain of patients operated on by video-thoracoscopic carcinologic surgery by counting them to a group of patients receiving standard general anesthesia with opioid.
Status | Completed |
Enrollment | 90 |
Est. completion date | April 30, 2023 |
Est. primary completion date | April 30, 2023 |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: - Adult patient - Patient operated on pulmonary carcinologic surgery by thoracoscopy of a foreseeable duration greater than 2 hours Exclusion Criteria: - Patient with unstable unstable unstable coronary artery disease, - Patient contraindicated for the use of dexmedetomidine: heart rate<50 / min, High degree atrioventricular block (2 and 3) unless fitted (carrier of a pacemaker), - Patient on beta-blocker, allergy to Dexdor®, - Patient allergic to other drugs used in OFA (Paracetamol and NSAIDs). - Renal insufficiency patient with creatinine clearance<30ml/min will not be excluded but will not receive NSAIDs. - Minor patient, - Adult patient under guardianship or curators. |
Country | Name | City | State |
---|---|---|---|
France | CHU de Nantes | Nantes |
Lead Sponsor | Collaborator |
---|---|
Nantes University Hospital |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Morphine consumption | Total morphine consumption over the first 48 post operative hours in milligrammes | Day 2 | |
Secondary | Preoperatory haemodynamic tolerance | Maximum doses of norepinephrine intraoperatively in µg/kg/min. | Day 0 | |
Secondary | Quality of intraoperative anesthesia | Duration of surgery (time between entering the operating room and leaving the room) in minutes. | Day 0 | |
Secondary | Ileus Postoperative | Presence of postoperative ileus (defined by the presence 2 of the following criteria from the 4th postoperative day: nausea and vomiting, absence of food recovery, no stool or gas in the last 24 hours, abdominal meteorism, radiological arguments) | Day 4 | |
Secondary | Duration of hospitalization | Length of hospitalization (Time between arrival at the hospital and discharge) in days. | Day 10 | |
Secondary | Chronic neuropathic pain | Evaluation of neuropathic pain (assessed by the DN 4 score:diagnosis of neuropathic pain) | Month-3 | |
Secondary | Long-term morphine consumption | Morphine consumption at 3-month (yes/no) | Month-3 | |
Secondary | Physical form recovery | Time between surgery and resumption of physical activity in days. | Month-3 |
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