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Clinical Trials in Turkey / NCT07400055
Starting soon Observational

MRI Evaluation of Spinal Cord Edema After CT-Guided Percutaneous Cordotomy in Cancer Pain Patients

NCT07400055 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-03-01
Last updated
2026-02-10

Condition(s) studied

Cancer PainIntractable PainSpinal Cord EdemaNeuropathic Pain

Investigational drug(s) / intervention(s)

CT-guided Percutaneous Cervical Cordotomy

CT-guided Percutaneous Cervical Cordotomy: Routine clinical percutaneous cervical cordotomy performed under CT guidance using radiofrequency ablation at the C1-C2 level for the treatment of intractable cancer pain.

Study summary

This observational study aims to evaluate changes in the spinal cord following CT-guided percutaneous cervical cordotomy performed for the treatment of intractable cancer-related pain. Cordotomy is a routine clinical procedure used to relieve severe pain in selected cancer patients. After the procedure, some patients may develop temporary neurological symptoms that are thought to be related to spinal cord edema.

In this study, magnetic resonance imaging (MRI) will be performed as part of routine clinical follow-up on postoperative day 1 and at 1 month to assess the presence and extent of spinal cord edema. Clinical outcomes, including pain intensity and possible postprocedural symptoms, will be recorded and compared with MRI findings.

The goal of this research is to better understand the relationship between imaging changes in the spinal cord and clinical outcomes after cordotomy, which may help improve patient care and postoperative management in the future.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Adults aged 18 years and older Patients with cancer-related pain refractory to medical treatment Patients scheduled to undergo CT-guided percutaneous cervical cordotomy as part of routine clinical care Ability to provide informed consent Availability for postoperative MRI follow-up on day 1 and at 1 month Exclusion Criteria: Patients younger than 18 years Patients without an indication for percutaneous cervical cordotomy Inability to undergo MRI (e.g., incompatible implants, severe claustrophobia) Patients who decline participation or withdraw consent Incomplete clinical or imaging follow-up data

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Mersin University Faculty of Medicine, Department of Algology Mersin Yenişehir

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07400055 on ClinicalTrials.gov ↗ ← All trials in Turkey