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Spinal or hemi-spinal anesthesia in fast-track total hip arthroplasty and total knee arthroplasty (THA and TKA), a prospective randomized controlled study in the Martini Hospital

Spinal or hemi-spinal anesthesia in fast-track total hip arthroplasty and total knee arthroplasty (THA and TKA), a prospective randomized controlled study in the Martini Hospital - Rapid Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON40716
Enrollment
600
Registered
2014-09-29
Start date
2014-12-02
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

anesthesie technieken bij orthopedische patienten spinal anesthesia versus hemi-spinal anesthesia

Interventions

None listed

Sponsors

Martini Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: primary TKA or THA patients older than 18 year

Exclusion criteria

Exclusion criteria: not a primary THA or TKA patients with a strong preferance for one or the two anesthesia methods patient who want general anesthesia patient with a contra-indication for spinal anesthesia

Design outcomes

Primary

MeasureTime frame
The main endpoint is conversion to general anesthesia which is a measure for effectiveness of (hemi-)spinal anesthesia.

Secondary

MeasureTime frame
Secondary outcomes are length of stay in the post anesthesia care unit (PACU), need for urinary catheterization, intra operative blood loss, motoric dysfunction, postoperative pain and opioid consumption, orthostatic intolerance and dizziness, postoperative nausea and vomiting, reduction in length of stay (LOS)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)