Greater Occipital Nerve Blockade in Veterans With Post-concussion Headache: Sub-study 2

NCT07796074 · Status: RECRUITING · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2026-08-31

No results posted yet for this study

Summary

Anesthetic greater occipital nerve (GON) blockade is a simple, inexpensive, and safe procedure that has demonstrable headache pain suppressing effects. In this study, Veterans with post-traumatic headache will be randomized to receive 0.0%, 0.05%, or 0.5% bupivacaine in bilateral GON blocks and the lasting (i.e., transitional) effects on headache frequency measured in a headache diary.

Conditions

  • Post-Traumatic Headache

Interventions

OTHER

Bupivacaine bilateral greater occipital nerve block

Three subcutaneous injections of 1 mL each will be injected on both sides of the occipital region around the greater occipital nerve.

Sponsors & Collaborators

  • VA Connecticut Healthcare System

    collaborator FED
  • National Headache Foundation

    collaborator UNKNOWN
  • Yale University

    lead OTHER

Principal Investigators

  • Emmanuelle Schindler, MD, PhD · VA Connecticut Healthcare System

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-09-01
Primary Completion
2027-09-30
Completion
2027-12-31
FDA Drug
Yes

Countries

  • United States

Study Locations

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07796074 on ClinicalTrials.gov