The Duration of Spinal Anaesthesia - a Prospective, Observational Cohort Study

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorNordsjaellands Hospital

About this trial

Today, surgery in an ambulatory setting is preferred for many reasons. Total hip and knee arthroplasty (THA and TKA) are now procedures where patients can be sent home on the same day of the surgical procedure. However, this requires substantial knowledge of factors affecting the length of hospital stay. In this prospective, observational cohort study, we will investigate factors that affect the duration of spinal anaesthesia which is often used in THA and TKA. The aim is to gather enough data to be able to determine how local anaesthetic volume and dose affect the duration of spinal anaesthesia. This will enable us to decide whether spinal anaesthesia is a good option when performing TKA and THA in an ambulatory setting.

Eligibility criteria

Qualifiers

Scheduled for elective orthopaedic surgical procedures performed in spinal anaesthesia

ASA 1-4.

Disqualifiers

Age < 18 years

Anticoagulant medication therapy not paused according ESAIC/ESRA 2022 guidelines

Local infection at the lumbar puncture site

Bleeding disorder

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

2,000 Participants
are grouped into 1 trial group

Sponsors and collaborators

Nordsjaellands Hospital

Lead sponsor

Aleris Hospital

Collaborator