Status:
RECRUITING
Preoperative Education for Less Outpatient Pain After Surgery (PELOPS)
Lead Sponsor:
Hospices Civils de Lyon
Conditions:
Outpatient Orthopedic Surgery
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
In 2015, more than 50% of surgical procedures were performed in outpatient settings. Successful pain management after outpatient surgery is crucial, and requires a perfect cooperation between caregive...
Eligibility Criteria
Inclusion
- Adults (age ≥ 18 years);
- Patients scheduled for outpatient orthopedic surgery
- ASA (American Society of Anesthesiology) I to III;
- Patients admitted for an outpatient intervention resulting in moderate to severe pain: eg: arthroscopy of the knee or shoulder, cruciate ligaments, shoulder block, medial patellofemoral ligament plasty (not exhaustive)
Exclusion
- Pregnant or lactating women
- Patients with contraindications to paracetamol and/or second-level analgesic and/or NSAIDs (hepatocellular insufficiency, respiratory insufficiency, substituted or unsubstituted drug addicts, allergy to one of the drugs, history of bleeding or digestive perforation during previous NSAID treatment, history of gastroduodenal ulcer, renal failure with clearance \<50mL / min, severe heart failure)
- Patients with preoperative chronic pain (outside operative site, known or detected by DN4)
- Patients admitted for an outpatient arthroplasty (excluded because they are subjected of a specific preoperative preparation)
- Persons deprived of their liberty by a judicial or administrative decision, persons under psychiatric care, persons admitted to a health or social establishment for other purposes than research
- Patient with a poor understanding of French
- Patient refusing to participate to the study
- Patient not affiliated to a social security regimen
- Patient participating in other interventional research except a routine care research (former regulation) and/or research with no interference with the primary endpoint analysis as determined by the investigator.
Key Trial Info
Start Date :
January 22 2019
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
March 22 2027
Estimated Enrollment :
414 Patients enrolled
Trial Details
Trial ID
NCT03754699
Start Date
January 22 2019
End Date
March 22 2027
Last Update
March 3 2025
Active Locations (1)
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1
Hospices Civils de Lyon - Hopital de la Croix Rousse - Anaesthesia Reanimation unit
Lyon, France, 69004