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NCT Number: NCT07834242

Anaesthesia for Hip and Knee Arthroplasty (SPIGA)

Beneficial and harmful effects of spinal versus general anaesthesia in patients undergoing hip and knee arthroplasty.

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Key information

About this study

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

  • Short-term perioperative outcomes (0-24h postoperatively)
  • Stratified analysis of anaesthetic regimens
  • Impact of preoperative clinical frailty

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Scheduled for elective primary elective hip or knee arthroplasty, including unicompartmental knee

Exclusion criteria

  • Scheduled for elective primary hip or knee arthroplasty, including unicompartmental knee
  • Age ≥ 18 years
  • Unable to communicate in written and/or spoken Danish Contraindications against either spinal or general anaesthesia

Treatment and study plan

spinal anaesthesia

Procedure

Spinal anaesthesia according to local practice, including optional sedation with sedative-hypnotic pharmacological agents

General anaesthesia

Procedure

General anaesthesia according to local practice

Primary outcomes

  1. Hospital-free days within 30 days

    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.

Secondary outcomes

  1. Major complications

    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.

  2. Quality of Recovery

    Time frame: 24 hours postoperatively

    Quality of Recovery-15 questionnaire (QoR-15)

Other outcomes

  1. Patient satisfaction with anaesthesia

    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.

  2. Health-related quality of life (EQ5D5L-VAS)

    Time frame: Postoperative day 30

    Evaluation of health-related quality of life using the EuroQol EQ5D5L- VAS questionnaire.

  3. Number of unplanned hospital-visits

    Time frame: Postoperative day 0-30

    Defined as the number of any unplanned contact with the emergency department, outpatient clinic, or other hospital department.

  4. Willingness to repeat the type of anaesthesia

    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.

  5. Day-case discharge

    Time frame: Postoperative day 0

    Number of patients assessed as eligible for day-case surgery being discharged on the day of surgery.

Sponsors and collaborators

Lead sponsor

Zealand University Hospital

Other

Registry information

Official study title

Spinal Versus General Anaesthesia for Hip and Knee Arthroplasty. The Randomised, Clinical, Multicentre SPIGA Trial

Acronym: SPIGA

Important dates

Study start
2026
Primary completion
2031
Study completion
2031
First posted
Sep 22, 2026
Registry last updated
Sep 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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