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Completed

NCT Number: NCT07576309

Repetitive GON Blockade for Menstrual Migraine

: The primary objective of this prospective, randomized, double-blind, placebo-controlled clinical trial is to evaluate whether repetitive bilateral greater occipital nerve (GON) blockade administered with a local anesthetic (0.5% bupivacaine) significantly reduces headache severity, attack duration, and the number of pain days in female patients with menstrual migraine compared to a placebo group (normal saline). Patients will receive injections twice a month for three months (seven days before the expected onset of menstruation and on the first day of menstruation).

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Key information

Age range

18 year–50 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Saglik Bilimleri Universitesi

Istanbul, 34668, Turkey (Türkiye)

About this study

Menstrual migraine (MM) is a highly prevalent and challenging migraine subtype triggered by fluctuations in estrogen and progesterone levels, particularly estrogen withdrawal during the perimenstrual period

  • This hormonal withdrawal sensitizes the trigeminovascular system and promotes the release of neuropeptides such as calcitonin gene-related peptide (CGRP)
  • Currently, there are no licensed prophylactic medications specifically developed for MM, making alternative and non-systemic treatments necessary

This study investigates the efficacy of a targeted peripheral neuromodulation approach using bilateral greater occipital nerve (GON) blockade. The underlying clinical rationale is that GON blockade timed to the perimenstrual period can modulate nociceptive transmission at the trigeminocervical complex (TCC) and decrease peripheral nerve excitability, thereby limiting the impact of cyclic hormonal fluctuations on the trigeminovascular system

. In this trial, a Latin square experimental design is utilized to ensure balanced randomization between the active treatment and placebo groups

  • Unlike single-injection protocols, the intervention is specifically synchronized with the patients' menstrual cycles, involving injections twice a month over a three-month period (seven days before menstruation and on the first day of menstruation)
  • By evaluating this specific timing and repetitive protocol, the study aims to establish whether perimenstrual-targeted GON blockade can serve as an effective, non-systemic, short-term prophylactic strategy for patients suffering from this refractory migraine subtype.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosed with pure menstrual migraine or menstrually related migraine according to the International Classification of Headache Disorders, 3rd edition (ICHD-3) diagnostic criteria.
  • A documented history of migraine attacks during the perimenstrual period (between days -2 and +3 relative to the onset of menstruation) in at least two of the last three menstrual cycles.

Exclusion criteria

  • Diagnosis of chronic migraine.
  • Presence of an additional primary or secondary headache disorder.
  • Pregnant or lactating.
  • Known hypersensitivity to local anesthetics.
  • Received an occipital nerve blockade within the last three months.
  • Presence of a significant neurological or systemic disease that could affect the outcome evaluation.

Treatment and study plan

0.5% bupivacaine

Drug

Bilateral greater occipital nerve (GON) blockade using a local anesthetic.

Normal Saline

Other

Bilateral greater occipital nerve (GON) blockade using placebo (normal saline).

Primary outcomes

  1. Change in headache severity evaluated using the Visual Analog Scale (VAS)

    Time frame: Baseline, Month 3, and Month 6

    Headache severity measured by VAS.

Secondary outcomes

  1. Change in monthly migraine attack frequency

    Time frame: Baseline, Month 3, and Month 6

  2. Change in number of headache days per month

    Time frame: Baseline, Month 3, and Month 6

  3. Change in mean attack duration in hours

    Time frame: Baseline, Month 3, and Month 6

  4. Change in monthly analgesic consumption

    Time frame: Baseline, Month 3, and Month 6

  5. Change in Migraine Disability Assessment (MIDAS) scores

    Time frame: Baseline, Month 3, and Month 6

Sponsors and collaborators

Lead sponsor

Saglik Bilimleri Universitesi

Other

Registry information

Official study title

Perimenstrual Repetitive Greater Occipital Nerve Blockade for Menstrual Migraine: A Randomized, Double-Blind, Placebo-Controlled Trial

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
May 8, 2026
Registry last updated
May 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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