About this trial
A single-center, prospective cohort trial aims to provide stronger evidence regarding the impact of degenerative spondylolisthesis on the clinical outcome of unilateral biportal endoscopy for lumbar spinal stenosis
Eligibility criteria
Qualifiers
Age range: 50-80 years
Diagnosis of LSS affecting 1-2 vertebral levels
Predominant manifestation of neurogenic intermittent claudication, with ineffective conservative treatment for at least 3 months
Presence of lumbar DS of less than grade II and absence of spine instability
Disqualifiers
Diagnosis of isthmic lumbar spondylolisthesis or lumbar DS of grade ≥II
Evidence of instability at the affected vertebral level (intervertebral angle change > 15° and/or vertebral translation ≥ 4.5 mm in standing flexion-extension radiographs of the lumbar spine)
History of prior surgery at the affected vertebral level
Presence of scoliosis with a Cobb angle >20º
Trial design
Treatments tested in this trial
- Not listed