spinal anaesthesia
ProcedureSpinal anaesthesia according to local practice, including optional sedation with sedative-hypnotic pharmacological agents
NCT Number: NCT07834242
Beneficial and harmful effects of spinal versus general anaesthesia in patients undergoing hip and knee arthroplasty.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Effective and safe anaesthesia is fundamental to perioperative care. Hip and knee arthroplasty are among the most frequently performed surgical procedures worldwide and are typically performed under either spinal or general anaesthesia. However, high-quality comparative evidence regarding the benefits and harms of these anaesthetic techniques remains limited and inconclusive.
Both techniques are associated with short- and long-term risks, including postoperative nausea and vomiting, hypotension, nerve injury, acute kidney injury, and respiratory and cardiovascular complications. In addition, they may differentially modulate the surgical stress response, potentially influencing postoperative recovery and risk of complications.
Objective:
To compare the benefits and harms of spinal versus general anaesthesia in patients undergoing hip or knee replacement. We hypothesise that spinal anaesthesia results in better postoperative outcomes than general anaesthesia.
Intervention:
Patients undergoing elective primary hip or knee arthroplasty will be randomised to receive either spinal or general anaesthesia, with randomisation stratified by participating centre.
Design:
The SPIGA trial is an investigator-initiated, multicentre, randomised, superiority clinical trial. Participants will be randomly allocated at a 1:1 ratio using a central, computer-generated randomisation sequence. A total sample size of 3000 participants was determined using simulation-based methods to provide at least 90% power to detect a prespecified minimally clinically important difference, corresponding to an increase of one hospital-free day in at least 10% of participants at a two-sided significance level of 0.05.
Planned sub-studies
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Spinal anaesthesia according to local practice, including optional sedation with sedative-hypnotic pharmacological agents
General anaesthesia according to local practice
Time frame: Postoperative day 0-30
Defined as the number of days within the first 30 days following hip or knee arthroplasty surgery during which a participant is alive and not admitted to a hospital.
Time frame: Postoperative day 0-30
A major complication is defined as a major intra- or postoperative adverse event occurring from the initiation of anaesthesia through 30 days postoperatively.
Time frame: 24 hours postoperatively
Quality of Recovery-15 questionnaire (QoR-15)
Time frame: 24 hours postoperatively
Assessed 24 hours postoperatively by asking patients to rate their satisfaction on a numeric rating scale (NRS) from 0-10, where 0 indicates not satisfied at all/completely dissatisfied and 10 indicates extremely satisfied/fully satisfied.
Time frame: Postoperative day 30
Evaluation of health-related quality of life using the EuroQol EQ5D5L- VAS questionnaire.
Time frame: Postoperative day 0-30
Defined as the number of any unplanned contact with the emergency department, outpatient clinic, or other hospital department.
Time frame: 24 hours postoperatively
Assessed at 24 hours postoperatively by asking participants whether they would choose the same type of anaesthesia again in case of future surgery.
Time frame: Postoperative day 0
Number of patients assessed as eligible for day-case surgery being discharged on the day of surgery.
Zealand University Hospital
Other
Spinal Versus General Anaesthesia for Hip and Knee Arthroplasty. The Randomised, Clinical, Multicentre SPIGA Trial
Acronym: SPIGA
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