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Durotomy in minimally invasive transforaminal lumbar interbody fusion (MIS TLIF) - frequency and management

Durotomy in minimally invasive transforaminal lumbar interbody fusion (MIS TLIF) - frequency and management

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00006135
Enrollment
400
Registered
2014-05-16
Start date
2014-07-21
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

M53.2 M43.1

Interventions

Group 1: Patients with minimally invasive transforaminal lumbar interbody fusion (MIS TLIF) procedure to describe the incidence of unintended durotomies as well as their characterization and managemen

Sponsors

Universitätsklinikum Freiburg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with minimally invasive transforaminal lumbar interbody fusion (MIS TLIF) procedure performed from 01/2006 - 03/2014.

Exclusion criteria

Exclusion criteria: Age of patient < 18 years.

Design outcomes

Primary

MeasureTime frame
Unintended intraoperative durotomy.

Secondary

MeasureTime frame
Body mass index of patients who are affected by unintended durotomy. Postoperative complications.

Countries

Germany

Contacts

Public ContactJan-Helge Klingler

Neurochirurgische Universitätsklinik Freiburg

jan-helge.klingler@uniklinik-freiburg.de+49 761 270 50010

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 5, 2026