NCT07367152

Brief Summary

This retrospective cohort study will review medical records of patients treated with intercostal nerve radiofrequency for intercostal neuralgia. The goal is to identify patient and clinical factors that are associated with treatment success after the procedure. Outcomes will be assessed using pain measures documented during routine follow-up visits, along with any recorded adverse events. No additional visits, tests, or interventions are required because this study uses previously collected clinical data.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jan 2018

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2018

Completed
7.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 30, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 30, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

January 16, 2026

Completed
10 days until next milestone

First Posted

Study publicly available on registry

January 26, 2026

Completed
Last Updated

January 26, 2026

Status Verified

January 1, 2026

Enrollment Period

7.9 years

First QC Date

January 16, 2026

Last Update Submit

January 16, 2026

Conditions

Keywords

Intercostal nervePulsed radiofrequencyConventional radiofrequencyUltrasound-guided

Outcome Measures

Primary Outcomes (1)

  • Treatment response at 6 months (IMMPACT-defined responder rate)

    Responder defined as ≥50% reduction or ≥4-point decrease in NRS-11 compared with baseline.

    6 months

Secondary Outcomes (1)

  • Change in NRS-11 pain score from baseline

    Baseline, 3 months, and 6 months

Study Arms (1)

Intercostal Nerve Radiofrequency Cohort

Adults with intercostal neuralgia who underwent ultrasound-guided intercostal nerve radiofrequency treatment (conventional or pulsed) as part of routine clinical care.

Procedure: Intercostal Nerve Conventional Radiofrequency Ablation (CRF)Procedure: Intercostal Nerve Pulsed Radiofrequency (PRF)

Interventions

Ultrasound-guided intercostal pulsed radiofrequency delivered at 42°C for 240 seconds.

Intercostal Nerve Radiofrequency Cohort

Ultrasound-guided intercostal nerve lesioning at 80°C for 90 seconds following sensory stimulation.

Intercostal Nerve Radiofrequency Cohort

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adults (≥18 years) with intercostal neuralgia who underwent ultrasound-guided intercostal nerve radiofrequency treatment (conventional or pulsed) in routine clinical care and had documented baseline and at least 6-month follow-up NRS-11 pain scores.

You may qualify if:

  • Age ≥ 18 years.
  • Diagnosis of intercostal neuralgia (post-traumatic, postherpetic, or idiopathic) with thoracic neuropathic pain for at least 1 month
  • Underwent ultrasound-guided intercostal nerve radiofrequency treatment (conventional radiofrequency ablation \[CRF\] or pulsed radiofrequency \[PRF\]) as part of routine clinical care
  • Documented baseline NRS-11 pain score prior to the procedure and follow-up NRS-11 data available through at least 6 months after treatment.

You may not qualify if:

  • Thoracic pain attributable to malignancy-related causes (e.g., active malignant invasion, spinal metastasis) or an intrathoracic mass
  • History of thoracic surgery at the corresponding thoracic dermatome level (e.g., thoracotomy or VATS)
  • Prior radiofrequency treatment at the same intercostal nerve site
  • Receipt of other interventional treatments targeting the intercostal nerve during the study period (e.g., cryoablation or chemical neurolysis)
  • Insufficient follow-up data (less than 6 months of follow-up NRS-11 documentation).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Mersin University Faculty of Medicine, Department of Algology

Mersin, Mersin, 33110, Turkey (Türkiye)

Location

Related Publications (2)

  • Huang X, Ma Y, Wang W, Guo Y, Xu B, Ma K. Efficacy and safety of pulsed radiofrequency modulation of thoracic dorsal root ganglion or intercostal nerve on postherpetic neuralgia in aged patients: a retrospective study. BMC Neurol. 2021 Jun 24;21(1):233. doi: 10.1186/s12883-021-02286-6.

  • Engel AJ. Utility of intercostal nerve conventional thermal radiofrequency ablations in the injured worker after blunt trauma. Pain Physician. 2012 Sep-Oct;15(5):E711-8.

MeSH Terms

Conditions

Neuralgia, Postherpetic

Condition Hierarchy (Ancestors)

NeuralgiaPeripheral Nervous System DiseasesNeuromuscular DiseasesNervous System DiseasesPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

January 16, 2026

First Posted

January 26, 2026

Study Start

January 1, 2018

Primary Completion

November 30, 2025

Study Completion

November 30, 2025

Last Updated

January 26, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

This is a retrospective study based on de-identified patient records. No individual participant data (IPD) will be shared. Only aggregated results may be published in scientific journals.

Locations