The Effectiveness of Ultra-Sound Guided Erector Spinae Block With Betamethasone for Management of Truncal Chronic Post Herpetic Neuralgia.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorCairo University

About this trial

To investigate the effectiveness of ultra-Sound guided Erector spinae block (ESB) with Betamethasone as an adjuvant to standard medical protocol in the management of truncal chronic post herpetic neuralgia.

Eligibility criteria

Qualifiers

Patients age between 18 and 75.

Patients with American Society of Anesthesiologists (ASA) II and III status.

Patients diagnosed with truncal chronic post herpetic neuralgia( neuropathic pain persistent for more than 3 months from the onset of rash appearance )

Disqualifiers

Patients unable to comprehend the informed consent.

Patients on long term opioid regimens.

Patients with impairment in hepatic (Alanine aminotransferase (ALT) >50 U/L, and/or Aspartate aminotransferase (AST): >45 U/L) or renal functions( creatinine level ≥1.5 mg/dL)

Patients on anti-coagulation regimens.

Trial design

Treatments tested in this trial

  • Medical management regimen
  • Erector spinae plane (ESP) block

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators