Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT07129811

Stellate Ganglion Block in Complex Regional Pain Syndrome

Led by Ankara City Hospital Bilkent · Updated on 2025-09-05

32

Participants Needed

1

Research Sites

41 weeks

Total Duration

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AI-Summary

What this Trial Is About

The aim was to investigate the effect of Stellate Ganglion Blockade, which will be applied in addition to conventional physical therapy, on pain and functionality in patients with poststroke complex regional pain syndrome.

CONDITIONS

Official Title

Stellate Ganglion Block in Complex Regional Pain Syndrome

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Volunteer male and female patients aged 18-75
  • Diagnosed with Complex Regional Pain Syndrome according to the IASP 2012 Diagnostic Criteria
  • Patient's pain level must be VAS >4
Not Eligible

You will not qualify if you...

  • Presence of existing neurological diseases other than rheumatic diseases and stroke
  • General impairment
  • Conditions that would constitute a contraindication to application, such as an open wound or sensory deficit in the application area
  • Presence of active infection
  • Presence of malignancy
  • Cognitive dysfunction (mini mental test result <23)

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

Ankara Bilkent City Hospital

Ankara, Çankaya, Turkey (Türkiye)

Actively Recruiting

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Research Team

S

Seher KALIÇ MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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