ConditionShoulder Surgery
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Hospital, Montpellier
About this trial
Despite the implementation of Enhanced Recovery After Surgery (ERAS) protocols incorporating multimodal analgesia and regional anesthesia, postoperative pain following shoulder surgery remains inadequately controlled. Percutaneous peripheral nerve stimulation (PPNS) represents a potential alternative strategy for postoperative pain management. This prospective randomized study aims to assess the efficacy of PPNS for postoperative pain control following shoulder surgery.
Eligibility criteria
Qualifiers
Patients aged over 18 years old
Patients scheduled for shoulder surgery under regional and general anesthesia
Disqualifiers
Outpatient surgery
Patients scheduled for magnetic resonance imaging (MRI)
Patients with an implanted pacemaker
Patients receiving chronic opioid therapy
Trial design
Treatments tested in this trial
- Experimental: Neurostimulation Group
- Control group
Treatment groups
60 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov