Actively Recruiting

Phase 4
Age: 18Years - 64Years
All Genders
NCT05605639

Phrenic Nerve Infiltration in Neck Pain

Led by University of Seville · Updated on 2024-12-11

60

Participants Needed

2

Research Sites

136 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Neck pain frequently present comorbidities in peridiaphragmatic organs. The innervation of these organs include the phrenic nerve. It is known that peridiaphragmatic organs trigger referred pain in the neck area. As well, previous studies have shown that visceral disorders increase sensitization in somatic tissues. This study aims to analyze the ability of phrenic nerve infiltration to diminish sensitization and improve neck symptoms in the absence of neurological, traumatic or infectious pathology that justifies the pain, by means of a randomized controlled trial.

CONDITIONS

Official Title

Phrenic Nerve Infiltration in Neck Pain

Who Can Participate

Age: 18Years - 64Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Over 18 and under 64 years old
  • Patients attending a physician or physical therapist with a main complaint of neck pain
  • Presence of any peridiaphragmatic visceral disorder
  • Agreement to participate by signing informed consent
Not Eligible

You will not qualify if you...

  • Neurological, traumatic, oncological, infectious, or rheumatic illness (including fibromyalgia, ankylosing spondylitis)
  • Uncooperative subject
  • Severe psychiatric illness
  • Loss of cognitive ability
  • Contraindication to phrenic nerve infiltration
  • History of head, spinal, or upper limb surgery
  • Neck pain infiltration in the previous 3 months
  • Physical therapy for neck pain in the previous 30 days

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Nacho Navarro Fisioterapia

Dos Hermanas, Seville, Spain, 41089

Actively Recruiting

2

Crux Roxa

Seville, Spain, 41008

Actively Recruiting

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Research Team

A

Angel Oliva Pascual-Vaca, Dr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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