Actively Recruiting

Age: 18Years - 75Years
All Genders
NCT07372430

Proximal Versus Distal Superior Cluneal Nerve Block in Entrapment Neuropathy

Led by Gaziosmanpasa Research and Education Hospital · Updated on 2026-01-28

54

Participants Needed

1

Research Sites

28 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Superior cluneal nerve (SCN) entrapment is an underdiagnosed cause of chronic low back and gluteal pain. Although diagnostic nerve block is considered the gold standard for confirming SCN entrapment, there is no consensus regarding the optimal injection approach. This prospective observational study aims to compare the clinical effectiveness of proximal and distal ultrasound-guided SCN block techniques in patients diagnosed with SCN entrapment. Pain intensity and functional outcomes will be evaluated over the follow-up period to assess differences between the two approaches.

CONDITIONS

Official Title

Proximal Versus Distal Superior Cluneal Nerve Block in Entrapment Neuropathy

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 75 years
  • Chronic low back and/or gluteal pain lasting longer than 3 months
  • Localized point tenderness and/or paresthesia on palpation over the unilateral posterior iliac crest
  • Clinical suspicion of superior cluneal nerve entrapment based on physical examination
  • Failure to respond to conservative treatment
  • Ability and willingness to provide written informed consent
Not Eligible

You will not qualify if you...

  • Active local or systemic infection
  • Cognitive impairment or psychiatric disorders interfering with study participation
  • History of malignancy or cancer-related pain
  • Uncontrolled diabetes mellitus or severe comorbid conditions adversely affecting general health
  • Pregnancy
  • Known allergy to the medications used in the injection
  • Prominent radicular pain associated with neurological deficit
  • History of interventional procedures applied to the lumbar region within the last 6 months
  • Initiation of another lumbar interventional or medical treatment during the follow-up period
  • Suspected bilateral superior cluneal nerve entrapment
  • Sphincter dysfunction related to neurological disease
  • Bleeding diathesis or coagulation disorders

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Health Sciences University Gaziosmanpaşa Physical Medicine and Rehabilitation Training and Research Hospita

Istanbul, Turkey (Türkiye), 34255

Actively Recruiting

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Research Team

T

Tugce Yavuz Mollavelioglu, M.D

CONTACT

T

tugba bayraktar celebioglu, M.D

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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