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Comparison of Surgical Outcomes Between Pre Sympathetic Plexus and Post Sympathetic Plexus Approach

Comparison of Surgical Outcomes Between Pre Sympathetic Plexus and Post Sympathetic Plexus Approach

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04891432
Enrollment
200
Registered
2021-05-18
Start date
2021-04-08
Completion date
2025-12-31
Last updated
2024-04-19

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

Conditions

Fusion of Spine, Sympathetic Nervous System

Brief summary

There would be no difference in the risk of sympathetic plexus damage between the pre sympathetic plexus approach and the post sympathetic plexus approach.

Detailed description

Compare the incidence of sympathetic chain injury between front and back of sympathetic approach in oblique lumbar interbody fusion

Interventions

oblique lumbar interbody fusion or direct lateral interbody fusion

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with lumbar degenerative disease needs a lateral lumbar interbody fusion of 1-2 segments between L2 to S1.

Exclusion criteria

* Patients who had previously had lumbar surgery * Patients with muscle weakness of motor grade III or lower * Patients with neuropsychiatric diseases such as depression * Patients with musculoskeletal disease, inflammatory musculoskeletal disease, or infection * Patients with cancerous disease * Patients who do not want to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
The rate of sympathetic plexus injuryPostoperative day oneThe number of patiensts with sympathetic symptom such as edema of the lower extremity, change of skin temperature, pain, or paresthesia without other medical conditions

Secondary

MeasureTime frameDescription
Other complicationsPostoperative 6 monththe number of patients with any other complication such as Injury of vascular structure, ureter, peritoneum, or bowel.

Countries

South Korea

Contacts

Primary ContactChi Heon Kim, MD
chiheon1@snu.ac.kr+82-2-2072-3398

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026