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Clinical Trials in Denmark / NCT06459986
Recruiting Observational

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

NCT06459986 · tracked via the Priya Life Science Denmark tracker
Sponsor
Nordsjaellands Hospital
Phase
Observational
Started
2024-06-03
Last updated
2026-01-20

Condition(s) studied

Orthopedic Disorder

Study summary

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

Sex
ALL
Min age
18 Years
Max age
100 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Scheduled for elective orthopaedic surgical procedures performed in spinal anaesthesia * ASA 1-4. Exclusion Criteria: * Age \< 18 years * Anticoagulant medication therapy not paused according ESAIC/ESRA 2022 guidelines * Local infection at the lumbar puncture site * Bleeding disorder * Unable to cooperate with the spinal anaesthesia procedure.

Primary outcome measure(s)

  • Duration of spinal anasthesia 1 — 12 hours
    Time from subarachnoid LA administration to Bromage score \< 3
  • Duration of spinal anaesthesia 2 — 12 hours
    Time from subarachnoid LA administration to Bromage score = 1

Trial sites (2)

FacilityCityRegionStatus
Anæstesiologisk Afd Hillerød Denmark Recruiting
Aleris-Ringsted Ringsted Denmark Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06459986 on ClinicalTrials.gov ↗ ← All trials in Denmark