SCN9A Gene Expression and Inflammatory Cytokines
NCT07532200 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 100
Last updated 2026-06-01
Summary
Voltage-gated sodium channels, especially Nav1.7 encoded by the SCN9A gene, are key regulators of nociceptive transmission. Upregulation of SCN9A has been associated with increased neuronal excitability and heightened pain perception. In parallel, inflammatory cytokines such as interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), and interleukin-1 beta (IL-1β) are known to sensitize peripheral nociceptors and reduce the efficacy of local anesthetics by modifying tissue environment and ion channel activity. However, the combined influence of SCN9A expression and inflammatory cytokines on anesthetic success in SIP has not been fully elucidated.
This prospective case-control study aims to evaluate the association between SCN9A gene expression and inflammatory cytokine levels with the clinical success of IANB in patients with SIP affecting mandibular molars. Approximately 90-100 patients will be recruited and categorized into two groups based on anesthetic outcome: successful anesthesia and failed anesthesia. All patients will receive a standardized IANB using 2% lidocaine with 1:100,000 epinephrine. Anesthetic success will be determined based on the absence of pain during access cavity preparation and instrumentation.
Following access and pulp extirpation, pulpal tissue samples will be collected. SCN9A gene expression will be assessed using quantitative real-time polymerase chain reaction (RT-qPCR), with relative expression calculated using the 2\^-ΔΔCt method. Inflammatory cytokine levels (IL-6, TNF-α, IL-1β) will be quantified using enzyme-linked immunosorbent assay (ELISA).
The primary outcome will be the difference in SCN9A expression between failed and successful anesthesia groups. Secondary outcomes will include comparison of cytokine levels and evaluation of correlations between SCN9A expression and inflammatory markers. Statistical analysis will include group comparisons, correlation analysis, logistic regression, and receiver operating characteristic (ROC) curve analysis to assess the predictive value of these biomarkers.
Conditions
- Pulpitis - Irreversible
Interventions
- PROCEDURE
-
Inferior Alveolar Nerve Block
All participants will receive a standardized inferior alveolar nerve block (IANB) administered using 2% lidocaine with 1:80,000 epinephrine. The injection will be performed using a conventional Halsted technique with a 27-gauge long needle under strict aseptic conditions. The needle will be inserted at the pterygomandibular raphe region, advancing until bony contact is achieved near the mandibular foramen. Following negative aspiration, approximately 1.8 mL of anesthetic solution will be deposited slowly over 60-90 seconds. Lip numbness will be assessed after 10-15 minutes to confirm nerve block onset. No additional anesthetic techniques will be used prior to the assessment of primary anesthetic success. Endodontic access cavity preparation will then be initiated, and pain response during access and initial instrumentation will be recorded using a standardized pain scale. Anesthetic success or failure will be determined based on the patient's pain response, as per predefined criteria.
Sponsors & Collaborators
-
Jamia Millia Islamia
lead OTHER
Eligibility
- Min Age
- 18 Years
- Max Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2026-04-10
- Primary Completion
- 2026-09-10
- Completion
- 2026-09-30
Countries
- India
Study Locations
More Related Trials
-
Analysis of Cortical Excitability in Neuropathic Pain
NCT00789347 ·Status: UNKNOWN
-
To Evaluate the Long-term Safety and Efficacy of HSK16149 in Chinese Patients With Peripheral Neuralgia
NCT05890053 ·Status: COMPLETED ·Phase: PHASE3
-
In Vitro Studies on Pharmacological Regulation and Genetic Risk Factors of Peripheral Human Nociceptors
NCT00223366 ·Status: COMPLETED
-
Injection Therapy for Neuropathic Pain
NCT05809700 ·Status: COMPLETED ·Phase: NA
-
An Evaluation of the Effect of a Surface Acoustic Wave Patch Device on the Symptons of Trigeminal Neuralgia
NCT02801630 ·Status: UNKNOWN ·Phase: NA
-
Efficacy Study of Botox to Treat Neuropathic Pain
NCT00527202 ·Status: COMPLETED ·Phase: PHASE4
-
Evaluation of Nicotinamide Riboside in Prevention of Small Fiber Axon Degeneration and Promotion of Nerve Regeneration
NCT03912220 ·Status: COMPLETED ·Phase: PHASE2
-
Treatment of Upper Cluneal Nerve Entrapment Syndrome for Reduction of Low Back Pain
NCT06059612 ·Status: COMPLETED ·Phase: NA
-
Efficacy, Safety, and Tolerability of SR750 in Patients With Trigeminal Neuralgia
NCT06571448 ·Status: COMPLETED ·Phase: PHASE2
-
Ear Acupuncture for Neuropathic Pain
NCT05052645 ·Status: WITHDRAWN ·Phase: NA
-
A Study to Investigate the Tolerability and Effects on Epidermal Nerve Fiber Density of Multiple Low-Concentrations of NGX-1998 in Healthy Volunteers
NCT00912262 ·Status: COMPLETED ·Phase: PHASE1
-
Study of Integrity of Down Inhibitor Bundle at Patients Suffering of Neuropathic Pain
NCT01053845 ·Status: COMPLETED ·Phase: PHASE1
-
Study in Neuropathic Pain Patients With Peripheral Nerve Injury
NCT00969059 ·Status: COMPLETED ·Phase: PHASE2
-
IV Lidocaine Infusion for Neuropathic Pain
NCT05731739 ·Status: WITHDRAWN
-
A Microneurography Study of NaV1.8 Inhibition in Healthy Adults
NCT06420765 ·Status: COMPLETED ·Phase: PHASE1
-
Exploring the Benefit of Neuromodulation in Treating Chemo-induced Peripheral Neuropathy Using Peripheral Neuropathy Markers (Meissner's Corpuscles and Epidermal Nerve Fiber Density) and Sensory Testing (Quantitative Sensory and Gait Testing): A Single Center Feasibility Study
NCT06121232 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Sodium Channel Mutations in Patient With the Anterior Cutaneous Nerve Entrapment Syndrome (ACNES)
NCT05877274 ·Status: UNKNOWN
-
Diagnostic Markers of Neuropathic Odontalgia
NCT04142918 ·Status: UNKNOWN
-
Coeliac Plexus Neurolysis Versus Splanchnic Nerve Neurolysis
NCT05541211 ·Status: RECRUITING ·Phase: NA
-
Efficacy and Safety of SAR292833 Administration for 4 Weeks in Patients With Chronic Peripheral Neuropathic Pain
NCT01463397 ·Status: COMPLETED ·Phase: PHASE2
-
Study to Evaluate the Efficacy of Lithium Carbonate in Spinal Cord Injury Patients With Neuropathic Pain
NCT01855594 ·Status: COMPLETED ·Phase: PHASE2
-
Study of NGX-4010 for the Treatment of Postherpetic Neuralgia
NCT00300222 ·Status: COMPLETED ·Phase: PHASE3
-
Neuropathic Pain Database
NCT00669006 ·Status: COMPLETED
-
Infusion Treatments of Chronic Peripheral Neuropathic Pain
NCT06297915 ·Status: COMPLETED
-
The Use of Zoledronic Acid to Complex Regional Pain Syndrome
NCT01788176 ·Status: UNKNOWN ·Phase: PHASE2