Migraine Medication Effects on Urinary Symptoms

NCT06212661 — Enrolling by invitation, 200 participants, The Cleveland Clinic

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RegistryNCT06212661
StatusEnrolling by invitation
Study typeObservational
Enrollment200 (Estimated)
SponsorThe Cleveland Clinic (Other)
ConditionsOveractive Bladder, Bladder Pain Syndrome, Migraine Disorders, Overactive Bladder Syndrome, Overactive Detrusor, Migraine, Interstitial Cystitis
InterventionsUbrogepant, Rimegepant, Atogepant, Eptinezumab, Fremanezumab, Galcanezumab, Erenumab, Botulinum toxin A (Drug)
Datesstart 2024-04-05, primary completion 2027-06-01 (estimated), completion 2027-12-01 (estimated), first posted 2024-01-19, last updated 2026-10-19
Locations1 site in United States

Related Papers Related Patents Related Grants Related Experts
All trials for Overactive Bladder All trials for Bladder Pain Syndrome All trials of Ubrogepant All trials of Rimegepant

-Summary

A prospective observational cohort trial to study the effects of CGRP inhibitors (CGRPi) on lower urinary tract symptoms (LUTS) and bladder/pelvic pain. Candidates for either CGRPi or an alternative therapy for refractory migraines (OnabotulinumtoxinA (BoNTA) extracranial muscle injections) with baseline LUTS will be recruited. The investigators will assess LUTS and pelvic pain using validated symptom and quality-of-life questionnaires, pretreatment and at 3 months post-treatment follow-up, comparing change in symptoms based on treatment received.

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+Detailed description

Common urinary urgency syndromes may be related to over-activation of bladder afferent pathways involving CGRP signaling. CGRP (calcitonin gene related protein) is a neurotransmitter in afferent pathways also involved in central nociception and hypersensitization. CGRP-targeted therapies, approved for migraine treatment, have the potential to alleviate lower urinary tract symptoms, but these possible effects have not been studied in humans.

This is a prospective observational cohort trial to study the effects of CGRP inhibitors (CGRPi) on lower urinary tract symptoms (LUTS) and bladder/pelvic pain. Candidates for either CGRPi or an alternative therapy for refractory migraines (OnabotulinumtoxinA (BoNTA) extracranial muscle injections) with baseline LUTS will be recruited. The investigators will assess LUTS and pelvic pain using validated symptom and quality-of-life questionnaires, pretreatment and at 3 months post-treatment follow-up, comparing change in symptoms based on treatment received.

+Arms and interventions

ArmTypeInterventionsDescription
CGRP inhibitorDrug: Ubrogepant; Drug: Rimegepant; Drug: Atogepant; Drug: Eptinezumab; Drug: Fremanezumab; Drug: Galcanezumab; Drug: Erenumab* Ubrogepant (Ubrelvy™) * Rimegepant (Nurtec®) * Atogepant (Qulipta™) * Eptinezumab (Vyepti®) * Fremanezumab (Ajovy®) * Galcanezumab (Emgality®) * Erenumab (Aimovig®) dosage and duration according to provider's clinical decision.
BoNTA extracranial muscle injectionsDrug: Botulinum toxin ABotolinum toxin A (Botox) Injection into extracranial muscles to treat migraine. Dosage and duration according to provider's clinical decision
  • Ubrogepant (Drug), also known as Ubrelvy: Ubrogepant (Ubrelvy™), oral, dosage at discretion of clinical provider, for treatment of migraine headaches.
  • Rimegepant (Drug), also known as Nurtec: Rimegepant (Nurtec®), oral, dosage at discretion of clinical provider, for treatment of migraine headaches.
  • Atogepant (Drug), also known as Qulipta: Atogepant (Qulipta™), oral, dosage at discretion of clinical provider, for treatment of migraine headaches.
  • Eptinezumab (Drug), also known as Vyepti: Eptinezumab (Vyepti®) injection, dosage at discretion of clinical provider, for treatment of migraine headaches.
  • Fremanezumab (Drug), also known as Ajovy: Fremanezumab (Ajovy®) injection, dosage at discretion of clinical provider, for treatment of migraine headaches.
  • Galcanezumab (Drug), also known as Emgality: Galcanezumab (Emgality®) injection, dosage at discretion of clinical provider, for treatment of migraine headaches.
  • Erenumab (Drug), also known as Aimovig: Erenumab (Aimovig®) injection, dosage at discretion of clinical provider, for treatment of migraine headaches.
  • Botulinum toxin A (Drug), also known as Botox: Botolinum toxin A (Botox) injections into extracranial muscles, dosage at discretion of clinical provider, for treatment of migraines.

+Outcome measures

Primary outcomes

  • changes in OAB symptoms [3 months]: To prospectively compare changes in OAB symptoms after beginning CGRP inhibitor treatment for migraine, with changes after beginning local BoNTA injections for migraine as controls. OAB symptom change will be measured using the International Consultation on Incontinence Questionnaire (ICIQ) - Female Lower Urinary Tract Symptoms (FLUTS). ICIQ-FLUTS questionnaire composite OAB score, including urgency, frequency, nocturia and urge incontinence domains (range: 0-16, higher scores indicate worse symptoms). Differences of 2-4 points with a standard deviation of 3-4 points were reported as significant in the literature.

Secondary outcomes

  • changes in bladder pain symptoms [3 months]: To prospectively compare changes in bladder pain symptoms after beginning CGRP inhibitor treatment for migraine, with changes after beginning local BoNTA injections for migraine as controls. Bladder / pelvic pain symptom change will be measured using the Female Genitourinary Pain Index (GUPI). The score ranges from 0 to 39, quality of life question score from 0 to 6, and higher scores indicate worse symptoms.
  • rates of LUTS and LUTS-related quality of life (QoL) in patients with chronic refractory migraine. [3 months]: To assess rates of LUTS (Lower Urinary Tract Symptoms) and LUTS-related quality of life (QoL) in patients with chronic refractory migraine. LUTS will be assessed using the International Consultation on Incontinence Questionnaire (ICIQ) - Female Lower Urinary Tract Symptoms (FLUTS). This questionnaire has 12 symptoms questions scored 0 to 4, overall questionnaire score is 0 to 48 points, and higher scores indicate worse symptoms. Bladder / pelvic pain symptoms will be measured using the Female Genitourinary Pain Index (GUPI). The score ranges from 0 to 39, higher scores indicate worse symptoms. LUTS-related quality of life question, adopted from the international prostate symptom score (IPSS) or American Urological Association symptom index (AUASI), is scored 0 to 6 and a higher score indicated worse quality of life.

+Eligibility

Sex: Female, ages: 18 Years to any

Inclusion Criteria:

* Female Patients > 18 years
* Refractory migraine, planned treatment with either:
* CGRP inhibitors, including:

  * CGRP small molecule receptor antagonists ("gepants"): Ubrogepant, Rimegepant, Atogepant.
  * CGRP monoclonal antibodies: Eptinezumab, Fremanezumab, Galcanezumab.
  * CGRP receptor monoclonal antibodies: Erenumab.
* BoNTA extracranial muscle injections
* Any of the following symptoms during the last month:

  * Urinating too often (frequency).
  * Having a sudden urge to urinate that's difficult to hold back (urgency).
  * Having a sudden urge to urinate and urine leaking before you make it to the toilet (urge incontinence).

Exclusion Criteria:

* Age < 18 years
* CGRP treatment within the last 12 months or BoNTA (head / bladder) last 6 months.
* Patient (or medical decision-maker) unable to provide informed consent or unable to answer questionnaire.
* Unable to urinate, eg: post cystectomy, indwelling catheter, on intermittent self catheterization, ESRD w/ anuria.
* Prior bladder BoNTA in last 12 months.

+Locations (1)

FacilityCityCountryStatus
Cleveland Clinic, Main CampusCleveland, OhioUnited States

+Investigators