Intravenous Dexamethasone Administration in Patients Undergoing Total Shoulder Arthroplasty

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age58-85
SponsorChristian Candrian

About this trial

The aim of the study is to evaluate if intravenous steroid supplementation can provide advantages over routine analgesia protocols in terms of post-operative symptoms (pain and nausea), length of hospital stay, shoulder range of motion, function and patient satisfaction

Eligibility criteria

Qualifiers

Patients undergoing unilateral primary total anatomical or reverse shoulder arthroplasty (Total Shoulder Arthroplasty)

Patients with a BMI >18.5 and <35

Patients able to provide informed consent and follow all the study procedures as indicated by the protocol

Informed Consent as documented by signature

Disqualifiers

Contraindications to steroids

Revision and post-traumatic TSA

Active steroid or immunosuppressive therapy in the last 30 days before the operation

Pregnant or breast-feeding women

Trial design

Treatments tested in this trial

  • dexamethasone

Treatment groups

74 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Christian Candrian

Lead sponsor

Ente Ospedaliero Cantonale, Bellinzona

Sponsor institution