| Registry | NCT06212661 |
|---|---|
| Status | Enrolling by invitation |
| Study type | Observational |
| Enrollment | 200 (Estimated) |
| Sponsor | The Cleveland Clinic (Other) |
| Conditions | Overactive Bladder, Bladder Pain Syndrome, Migraine Disorders, Overactive Bladder Syndrome, Overactive Detrusor, Migraine, Interstitial Cystitis |
| Interventions | Ubrogepant, Rimegepant, Atogepant, Eptinezumab, Fremanezumab, Galcanezumab, Erenumab, Botulinum toxin A (Drug) |
| Dates | start 2024-04-05, primary completion 2027-06-01 (estimated), completion 2027-12-01 (estimated), first posted 2024-01-19, last updated 2026-10-19 |
| Locations | 1 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
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.
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.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| CGRP inhibitor | Drug: 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 injections | Drug: Botulinum toxin A | Botolinum toxin A (Botox) Injection into extracranial muscles to treat migraine. Dosage and duration according to provider's clinical decision |
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.| Facility | City | Country | Status |
|---|---|---|---|
| Cleveland Clinic, Main Campus | Cleveland, Ohio | United States |