Patient-Related Factors Influencing Greater Occipital Nerve Blockade Response in Medication-Overuse Headache
This observational study aims to identify patient-related factors that influence the response to greater occipital nerve blockade in medication-overuse headache, by examining the number of days you use analgesics for headache in the past month.
Data Collection
Collected at a single point in time - Cross-sectionalBrain Diseases+7
+ Central Nervous System Diseases
+ Headache
Case-Control
Comparing exposures between individuals with and without disease in order to identify potential risk factors.Summary
Study start date: March 17, 2026
Actual date on which the first participant was enrolled.This study focuses on understanding the factors that may affect the response to treatment in individuals with medication-overuse headache. This condition occurs when a person uses pain-relieving medication too often, causing the medicine to lose effectiveness and the headaches to become more frequent. The study specifically looks at patients who undergo a procedure called ultrasound-guided greater occipital nerve block, a treatment that involves injecting medication around the occipital nerves located at the back of the head to block pain signals. The goal is to identify pre-treatment patient characteristics that could influence the success of this procedure. During the study, participants will be asked about their use of pain-relieving medication for headaches over the past month. The primary outcome measured is the total number of days on which they used these analgesics. This information helps the researchers evaluate the effectiveness of the greater occipital nerve block in reducing the need for pain medication and potentially improving the quality of life for individuals with medication-overuse headache.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.70 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Case-Control
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 65 Years
Range of ages for which participants are eligible to join.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Sultan 1. Murat State Hospital
Edirne, Turkey (Türkiye)Open Sultan 1. Murat State Hospital in Google Maps