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NCT07633730Recruiting

Efficacy of the Erector Spinae Plane Block for Persistent Back Pain in Patients With Ankylosing Spondylitis

Source: ClinicalTrials.gov · Last updated 8 Jun 2026

Brief summary (registry, in English)

Despite adequate control of disease activity with standard medical therapies, there remains an ongoing need for complementary and interventional approaches for the management of persistent back pain in patients with ankylosing spondylitis. Although the erector spinae plane block has been described in the literature as a safe and effective analgesic intervention for chronic back pain in various patient populations, to the best of our knowledge, no clinical study has specifically evaluated its use for persistent back pain in patients with ankylosing spondylitis receiving medical treatment. Therefore, the present study aims to evaluate the effects of erector spinae plane block on pain severity and clinical outcomes in patients with ankylosing spondylitis whose disease activity is controlled under treatment but who continue to experience persistent back pain.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
15 (estimated)
First submitted
2 Jun 2026
Start date
Jun 2026
Primary completion date
May 2027
Lead sponsor
Marmara University
NCT number
NCT07633730

What you commit to

  • Study type: Interventional
  • Planned participants: 15
  • From Jun 2026 to the primary completion date, May 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of thoracic surgery
  • Presence of major psychiatric comorbidity
  • History of bleeding diathesis
  • Presence of active local and/or systemic infection
  • Known allergy to the medications to be injected
  • Active phase of the disease (elevated acute phase reactants, active arthritis findings, etc.)

Other

  • Body mass index (BMI) greater than 35 kg/m²
  • Intellectual disability or mental retardation
  • Congenital spinal anomaly
  • Pregnancy
  • Hemodynamic instability

Who the study is looking for

  • Age between 18 and 65 years
  • Diagnosis of ankylosing spondylitis according to the Modified New York Criteria
  • Patients receiving ongoing treatment with controlled disease activity but persistent back pain
  • Willingness to participate in the study

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Marmara University Faculty of Medicine Pendik Training and Research Hospital
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Recruiting

This page is information, not medical advice. Discuss any trial with your doctor.