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Clinical Trials in Turkey / NCT07596823
Recruiting Observational

Hematological Indices and Sympathetic Block Response in Neuropathic Pain

NCT07596823 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-06-01
Last updated
2026-06-29

Condition(s) studied

Neuropathic PainNeuropathic Pain Diagnostic Questionnaire (DN4) ≥ 4

Study summary

This prospective observational study aims to evaluate the relationship between hematological inflammatory indices and clinical treatment response in patients with neuropathic pain undergoing sympathetic nerve block procedures as part of routine clinical care. Hematological parameters including neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), monocyte-to-lymphocyte ratio (MLR), systemic immune-inflammation index (SII), systemic inflammation response index (SIRI), aggregate index of systemic inflammation (AISI), and red cell distribution width (RDW) will be evaluated before and after treatment. The association between changes in these indices and pain outcomes will be analyzed.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥18 years * Diagnosis of neuropathic pain based on clinical evaluation * DN4 and/or LANSS scores compatible with neuropathic pain * Undergoing sympathetic nerve block as part of routine clinical treatment * Availability of pre-treatment and follow-up hemogram parameters * Ability to provide written informed consent Exclusion Criteria: * Age \<18 years * Active infection or acute inflammatory disease * Active malignancy * History of hematological disease * Immunosuppressive therapy or systemic corticosteroid use * Major surgery or severe trauma within the last month * Pregnancy or breastfeeding * Autoimmune or rheumatologic inflammatory disease * Missing follow-up data

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ankara Bilkent City Hospital Ankara Cankaya Recruiting

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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 NCT07596823 on ClinicalTrials.gov ↗ ← All trials in Turkey