Status:
UNKNOWN
The Effect of a Developed Perioperative Rehabilitation Pathway Following Lumbar Arthrodesis
Lead Sponsor:
Universitaire Ziekenhuizen KU Leuven
Collaborating Sponsors:
KU Leuven
UHasselt
Conditions:
Physical Disability
Low Back Pain, Recurrent
Eligibility:
All Genders
18-75 years
Phase:
NA
Brief Summary
To compare the current rehabilitation pathway with the implementation of a newly developed rehabilitation pathway for patients with a single and double level lumbar arthrodesis.
Detailed Description
This involves a prospective interventional study with a one year follow-up. The investigators will compare the outcomes of the current rehabilitation pathway with a newly developed (based on systemati...
Eligibility Criteria
Inclusion
- Lumbar single and double level arthrodesis
- Signed informed consent
- Posterior Lumbar interbody fusion (PLIF), Posterolateral lumbar fusion (PLF) and Transforaminal lumbar interbody fusion (TLIF)
Exclusion
- Previous arthrodesis in the lumbar spine
- Musculoskeletal disorders which interfere with functional outcome, f.e. severe lower limb problems not related to the lumbar surgery
- Presence of one of the following pathologies:Parkinson Multiple sclerose (MS), Cerebral vascular accident (CVA), Peripheral neuropathies, Circulatory disorders, Gout, Rheumatoid disorders, Neoplasia, Septic arthritis, Pregnancy, Vestibular disorder, Infectious diseases
- Accident at work or lawsuit
- Low cognition
- Not able to speak Dutch
Key Trial Info
Start Date :
January 3 2018
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2024
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT03427099
Start Date
January 3 2018
End Date
December 31 2024
Last Update
January 3 2024
Active Locations (1)
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1
UZ/KU Leuven
Leuven, Vlaams Brabant, Belgium, 3000