Trials / Enrolling By Invitation
Enrolling By InvitationNCT07053176
Impact of Local Lidocaine Paravertebral Cervical Injection on Cervicogenic Dizziness Symptoms
Usefullnes of Local Lidocaine Paravertebral Cervical Injection on Cervicogenic Dizziness Symptoms Management: a Randomzied Clinical Trial
- Status
- Enrolling By Invitation
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 42 (estimated)
- Sponsor
- Uniter Onlus · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
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.
Detailed description
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. subjective testing will include dizziness handicap inventory, Neck Disability Index, Neck Pain Intensity, Tampa Scale for Kinesiophobia, Hospital Anxiety and Depression Scale. Objective testing will include cervical range of motion, joint position error and static posturography testing.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| 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 |
Timeline
- Start date
- 2025-08-01
- Primary completion
- 2025-09-15
- Completion
- 2025-09-15
- First posted
- 2025-07-08
- Last updated
- 2025-07-08
Locations
1 site across 1 country: Italy
Source: ClinicalTrials.gov record NCT07053176. Inclusion in this directory is not an endorsement.