Feasibility Evaluation of the LimiFlex Spinal Stabilization System in the Treatment of Degenerative Spondylolisthesis

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00006034

Enrollment

Registered

2014-04-30

Start date

2012-12-03

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

M48.07 M43.17

Interventions

Group 1: dorsal decompression and spinal stabilisation with LimiFlex

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: diagnosis of advanced stenosis of the lumbar spinal canal with or without additional degenerative spondylolisthesis grade 1-2.

Exclusion criteria

Exclusion criteria: Patients who are allergic or intolerant to titanium and/or polyethylene and patients with tumors, infections, severe osteoporosis or other conditions that make appropriate fixation of the implant impossible, women who are pregnant or planning a pregnancy

Design outcomes

Primary

Measure	Time frame
Painlevel measured by visual analogue scale and function measured by oswestry disability index after 3, 6, 12 and 24 months	—

Countries

Germany

Contacts

Public ContactRobert Pflugmacher

Orthopädie und Unfallchirurgie Univeritätsklinikum Bonn

robert.pflugmacher@gmail.com0228-287-13751

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026