A Registry-Based Cohort Study on the Clinical Outcomes of Spinal Cord Glioma Resection Via the Dorsolateral Sulcus Approach

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age3-75
SponsorBeijing Tiantan Hospital

About this trial

Spinal cord gliomas are the most common type of primary intramedullary malignant tumors, with a low incidence and a peak onset age of approximately 35 years. They are slightly more prevalent in males than females. Clinical manifestations vary depending on tumor characteristics and location, typically presenting with axial pain and displaying a tendency for unilateral, infiltrative growth. Prognosis is generally poor, and effective treatment options are limited aside from surgical resection. Common surgical approaches for intramedullary tumor removal include the posterior median sulcus approach, the dorsolateral sulcus approach, and surface entry techniques.

Preliminary clinical observations suggest that the dorsolateral sulcus approach may offer superior preservation of neurological function and quality of life. However, due to limited research evaluating the safety and efficacy of different surgical routes, the traditional posterior median sulcus approach remains widely used.

This single-center, registry-based cohort study aims to compare the outcomes of spinal cord glioma resection via the dorsolateral sulcus approach versus the posterior median sulcus approach. Patients with laterally located tumors undergoing surgical treatment, classified according to the 2021 WHO criteria, will be included. Neurological function scores and quality-of-life assessments will be used to evaluate prognosis and survival, in order to determine the optimal surgical approach for spinal cord glioma resection.

Eligibility criteria

Qualifiers

Age between 3 and 75 years

Undergoing surgical resection of spinal cord tumor

Histopathological diagnosis of spinal cord glioma based on routine pathological examination

Availability of complete clinical data and willingness to participate in follow-up

Disqualifiers

Age under 3 years or over 75 years

Receipt of radiotherapy, chemotherapy, or anti-tumor biological therapy within 1 month prior to enrollment

Receipt of immunotherapy within 3 months prior to enrollment

Participation in other clinical trials within 3 months prior to enrollment

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

100 Participants
are grouped into 2 trial groups

Sponsors and collaborators