Trials / Recruiting
RecruitingNCT07487649
Treatment Response in Patients With Medication-Overuse Headache
Factors Affecting Treatment Response in Patients With Medication-Overuse Headache Undergoing Greater Occipital Nerve Blockade
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 70 (estimated)
- Sponsor
- Sultan 1. Murat State Hospital · Other Government
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- —
Summary
The aim of this study to evaluate pre-injection patient-related factors that may influence treatment response in patients with medication-overuse headache who underwent ultrasound-guided greater occipital nerve block.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Treatment outcome | Before the injection, patients will be evaluated for the number of headache days, headache severity, the number of days of analgesic use for headache, headache-related disability, pressure pain threshold over the bilateral greater occipital nerve, anxiety and depression scores, and sleep quality. At 1 and 2 months after the injection, they will be reassessed for the number of headache days, headache severity, and the number of days of analgesic use for headache. In addition, at 1 hour after the injection, the pain experienced during the injection procedure will be assessed. |
Timeline
- Start date
- 2026-03-17
- Primary completion
- 2026-05-30
- Completion
- 2026-05-30
- First posted
- 2026-03-23
- Last updated
- 2026-03-23
Locations
1 site across 1 country: Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT07487649. Inclusion in this directory is not an endorsement.