NCT07068451

Brief Summary

This study looked at two types of nerve block injections used to treat people with cervicogenic headache (CEH) and occipital neuralgia (ON)-two painful conditions that often cause pain at the back of the head and neck. The injections target nerves in the upper neck that may be causing the pain. The researchers compared: One nerve injection (greater occipital nerve block, or GONB), versus Two nerve injections (GONB plus lesser occipital nerve block, or LONB).

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
160

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jan 2020

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2020

Completed
3.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2023

Completed
2.2 years until next milestone

First Submitted

Initial submission to the registry

June 26, 2025

Completed
20 days until next milestone

First Posted

Study publicly available on registry

July 16, 2025

Completed
Last Updated

July 16, 2025

Status Verified

July 1, 2025

Enrollment Period

3.2 years

First QC Date

June 26, 2025

Last Update Submit

July 6, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Change in pain intensity measured by the Visual Analog Scale (VAS)

    ain intensity was assessed using a 10-point Visual Analog Scale (VAS), with 0 indicating no pain and 10 indicating the worst pain imaginable. VAS scores were recorded at baseline and follow-up visits.

    Baseline, 24 hours, 3 weeks, and 3 months post-intervention

Study Arms (2)

GONB Alone

EXPERIMENTAL

Patients received a single injection of 1 mL of 2% lidocaine at the greater occipital nerve using a landmark-guided technique.

Procedure: Greater Occipital Nerve Block (GONB)

GONB + LONB (Dual Block)

EXPERIMENTAL

Patients receive two injections of 1 mL of 2% lidocaine each at the greater and lesser occipital nerves using a landmark-guided technique.

Procedure: Combined Greater and Lesser Occipital Nerve Block (GONB + LONB)

Interventions

A landmark-guided injection of 1 mL of 2% lidocaine administered at the anatomical location of the greater occipital nerve (GON) to treat cervicogenic headache and occipital neuralgia. Performed without corticosteroids or imaging guidance.

Also known as: Drug: Lidocaine 2%
GONB Alone

Two landmark-guided injections of 1 mL of 2% lidocaine each at the anatomical locations of the greater and lesser occipital nerves. Performed without corticosteroids or imaging, targeting broader nerve involvement in cervicogenic headache and occipital neuralgia.

Also known as: Drug: Lidocaine 2%
GONB + LONB (Dual Block)

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may not qualify if:

  • Previous nerve block or other interventional procedures for headache
  • Use of systemic corticosteroids within the past 3 months
  • Known allergy to lidocaine or other amide-type local anesthetics
  • Evidence of secondary causes of headache on imaging (e.g., tumor, infection)
  • Pregnancy or breastfeeding
  • Active infection at the injection site
  • Coagulopathy or use of anticoagulant therapy
  • Significant psychiatric or neurological comorbidities interfering with study participation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Latakia

Latakia, Syria

Location

Related Links

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr

Study Record Dates

First Submitted

June 26, 2025

First Posted

July 16, 2025

Study Start

January 1, 2020

Primary Completion

April 1, 2023

Study Completion

April 1, 2023

Last Updated

July 16, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations