Perioperative Dexamethasone Reduces Postoperative Pain and Nausea After Periacetabular Osteotomy
Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-99
SponsorBalgrist University Hospital
About this trial
The purpose of this study is to assess the effect of Dexamethasone on postoperative pain and nausea after periacetabular osteotomy.
Eligibility criteria
Qualifiers
Age ≥ 18 years
General anasthesia
Elective periacetabular osteotomy for any reason
Written informed consent as documented by signature (Appendix Informed Consent Form)
Disqualifiers
Chronic pain patient, chronic lower back pain
Steroid or immunosuppressive drugs used within 6 months of surgery
Renal failure, hepatic failure
Relevant allergies
Trial design
Treatments tested in this trial
- Dexamethasone 4 Mg/mL Injectable Solution
- NaCl 0.9%
Treatment groups
60 Participants
are divided into 2 treatment groupsLocations
1Uniklinik Balgrist8008, Zurich Switzerland
Sponsors and collaborators
Balgrist University Hospital
Lead sponsor
Source ClinicalTrials.gov