Effect of Degenerative Spondylolisthesis on the Clinical Outcome of Unilateral Biportal Endoscopy for Lumbar Spinal Stenosis: Study Protocol

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age50-80
SponsorBeijing Friendship Hospital

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

Trial groups

150 Participants
are grouped into 2 trial groups

Sponsors and collaborators