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ENROLLING BY INVITATION
NCT07053176
PHASE4

Impact of Local Lidocaine Paravertebral Cervical Injection on Cervicogenic Dizziness Symptoms

Sponsor: Uniter Onlus

View on ClinicalTrials.gov

Summary

at least 42 patients affected by cervicogenic dizziness will be allocated to the experimental group or in the placebo group. in the first group patients will received 2 paravertebral intramuscular injection of lidocaine 0.5% while in the placebo group they will received saline solution with the same injection technique. patients will be evaluated by subjective and objective testing before the treatment, immediatly and 3 months after the treatment.

Official title: Usefullnes of Local Lidocaine Paravertebral Cervical Injection on Cervicogenic Dizziness Symptoms Management: a Randomzied Clinical Trial

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

42

Start Date

2025-08-01

Completion Date

2025-09-15

Last Updated

2025-07-08

Healthy Volunteers

No

Interventions

DRUG

0.5% Lidocaine

0.5% lidocaine injection will be administered in the paravertebral intramuscular region with 12 mm, 30 G needle from C2 to C7 bilaterally

DRUG

Saline Solution (NaCl 0,9%)

saline solution will be administered bilaterally in the paravertebral intamuscular region from C2 to C7 with 12 mm 30 G needle

Locations (1)

Uniter Onlus

Fara in Sabina, Rieti, Italy