Under construction – not a live service
Sign in
TerminatedNo phase

Surgery Induced Trauma After Total Versus Medial Unicompartmental Knee Arthroplasty (SITA)

Reason given: The study was terminated due to poor participant accrual. Recruitment was limited by competing clinical studies at the participating site, and the resources required to prolong the recruitment period were not available.

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

Trial details

Who runs it
Hvidovre University Hospital
Trial code
NCT05735847
Record updated
22 September 2026
Original description
Osteoarthritis (OA) is the most common type of arthritis, characterized by pain and physical disability. More than 10% of persons > 55 years have symptomatic OA, primarily involving the knees. Knee arthroplasty is considered a successful orthopaedic procedure in progressed knee OA (KOA) with severe pain and disability where non-surgical treatments have been tried.Read full original descriptionShow less

Does Surgery-Induced Trauma Influence Postoperative Safety and Outcome Comparing Total vs. Medial Unicompartmental Knee Arthroplasty (SITA): A Prospective Cohort Study

Osteoarthritis (OA) is the most common type of arthritis, characterized by pain and physical disability. More than 10% of persons > 55 years have symptomatic OA, primarily involving the knees. Knee arthroplasty is considered a successful orthopaedic procedure in progressed knee OA (KOA) with severe pain and disability where non-surgical treatments have been tried.

It has long been recognized that injury to the body, either from trauma or surgery causes an inflammatory response. As TKA is considered a more invasive procedure compared with UKA, TKA and UKA may not trigger inflammatory reactions of the same magnitude. Differences in inflammatory response between TKA and UKA could help explain why differences in outcome are present, despite both procedures being technically successful.

Even though knee arthroplasty is a very common and successful procedure, there are no existing studies comparing the invasiveness of TKA and UKA. As morbidity and mortality rates differ between the groups, the aim of this prospective cohort study is to investigate whether the post-operative inflammatory responses differ between TKA and UKA, and secondarily whether this difference can explain the difference in outcome between the two procedures.

The investigators hypothesize that TKA generates a larger postoperative systemic inflammatory response compared with UKA due to more extensive periarticular soft tissue and bone trauma.

The study's primary outcome is C-reactive Protein (CRP) measured in blood 24 hours after surgery (22-26 hours after surgery ~ day 1).

Participants which are candidates for either a TKA or a UKA will through serial blood test measurement have their postoperative systemic inflammatory response measured. This further will be correlated to the clinical and functional outcomes over a 2-years postoperative follow-up period.

Inclusion: Age 18 or more; A clinical and radiological diagnosis of knee OA; Candidate for spinal anaesthesia; signed informed consent.

Exclusion: Planned surgery within the observation period other than KA; Any contraindications to the use of torniquet during surgery; Any contraindication to the administration of pre-operative dexamethasone; Previous infection of the target knee joint; Injection of medication or substances in the target knee within 3 months prior to participation; Current systemic treatment with glucocorticoids equivalent to > 7.5 mg prednisolone/day; Surgery requiring spinal/general anaesthesia within the last 3 months prior to inclusion; Infection requiring medical/surgical treatment within the last 4 weeks prior to surgery for KA; Known autoimmune and/or inflammatory disease e.g. colitis ulcerosa; Active cancer diagnosis with ongoing treatment; Any other condition or impairment that, in the opinion of the investigator (or his/her delegate), makes a potential participant unsuitable for participation or which obstruct participation; KA indication due to sequelae of e.g. fracture(s); Immuno-inflammatory arthritis as cause of knee OA; Neurological dysfunction compromising mobility; Inability to understand or read Danish incl. instructions and questionnaires.

ClinicalTrials.gov NCT05735847