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Management of Seroma After Posterior Lumbar Spine Decompression

Management of Seroma After Posterior Lumbar Spine Decompression

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07060781
Enrollment
50
Registered
2025-07-11
Start date
2025-07-19
Completion date
2025-12-30
Last updated
2025-07-22

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

Conditions

Lumbar Spine Decompression, Seroma

Brief summary

The aim of this study is to evaluate the clinical presentation and management strategies of seroma formation following posterior lumbar spine decompression.

Detailed description

Posterior lumbar spine decompression is a widely employed surgical approach to alleviate neural element compression due to degenerative spinal conditions such as spinal stenosis, spondylolisthesis, and disc herniation. While generally effective in reducing symptoms and improving quality of life, this procedure is not without risk. Seroma formation, in particular, may follow posterior decompressive surgery or fusion and is thought to arise from the accumulation of lymphatic or serous fluid in the dead space created by tissue dissection.

Interventions

PROCEDUREPosterior Lumbar Spine Decompression

Patients undergoing elective posterior lumbar spine decompression.

Sponsors

Kafrelsheikh University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years. * Both sexes. * Patients undergoing elective posterior lumbar spine decompression.

Exclusion criteria

* History of previous lumbar spine surgery. * Active spinal infection, trauma, or malignancy. * Severe medical comorbidities that contraindicate surgery or influence wound healing (e.g., uncontrolled diabetes, immunosuppression, severe cardiovascular disease). * Patients unfit for general anesthesia.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of seroma6 months postoperativelyIncidence of seroma formation following posterior lumbar spine decompression will be recorded during hospitalization and at scheduled postoperative follow-up visits at 2 weeks, 6 weeks, 3 months, and 6 months.

Secondary

MeasureTime frameDescription
Number of aspirations required6 months postoperativelyNumber of aspirations required will be recorded.
Seroma recurrence rate6 months postoperativelySeroma recurrence rate will be recorded.
Association with patient risk factor6 months postoperativelyAssociation with patient risk factor will be recorded.

Countries

Egypt

Contacts

Primary ContactAyman M Basha, MD
aymanbasha424@gmail.com00201063037278

Outcome results

None listed

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