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Determination of Longus Colli Muscle Thickness by Ultrasonography

I

Istanbul University

Status

Completed

Conditions

Complex Regional Pain Syndromes
Hyperhidrosis
Pain Syndrome
Pain, Intractable

Study type

Observational

Funder types

Other

Identifiers

NCT05108103
2021/182

Details and patient eligibility

About

This study aims to assess the longus colli muscle thickness by ultrasonography in order to guide stellate ganglion blocks

Full description

Stellate ganglion block is an interventional pain management procedure that is often performed for diagnostic and therapeutic purposes. It has long been performed with the guidance of fluoroscopy, and despite the increasing use of ultrasonography in recent years, fluoroscopy is still the gold standard method.

In traditional fluoroscopic method, the needle is directed to the transverse process of the C6 vertebra, after touching the anterior tubercle (Chassaignac's tubercule) the needle is slightly withdrawn and following a negative aspiration, injection is performed.

The ideal placement of the needle should be anterolateral to the longus colli muscle and deep to the prevertebral fascia. Further placement may cause intramuscular spread and superficial placement may cause injection in the carotid sheath or vascular structures. These are the most important reasons for clinical ineffectiveness. How far should the needle be withdrawn? Data is inconsistent in the literature.

The primary aim of this study is to determine the distance from transverse process to longus colli muscles anterior border and from transverse process to carotid sheath's posterior border. Secondary aim is to investigate the relationship between longus colli muscle thickness and age, gender, height, weight, BMI and neck circumference.

Enrollment

200 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age between 18 - 65 years,
  • Giving informed consent for examination, ultrasonographic evaluation and study participation

Exclusion criteria

  • Having a chronic neck pain for more than 6 months,
  • Having any neurological or musculoskeletal conditions that may affect the anatomy of cervical region (cervical disc herniation, torticollis, severe scoliosis, vertebral malformation, spinal stenosis, myopathies, etc.)
  • Having a history of surgery or radiation therapy in the cervical region

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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