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RecruitingNCT07773532Updated Nov 3, 2026

Predictive Value of Inflammatory Biomarkers for Mirabegron Response in Women With Overactive Bladder

An observational study in Overactive Bladder (OAB), sponsored by Bagcilar Training and Research Hospital. Recruiting at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-03.

Sponsored by Bagcilar Training and Research Hospital · Observational

Updated Nov 3, 2026Now RecruitingSite recruiting status changed+4 moreGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
115
Ages
18 Years and older
Sex
Female
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Study summary

Overactive bladder (OAB) is associated with systemic chronic inflammation. Indices derived from complete blood count (such as neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and systemic immune-inflammation index (SII)) have shown associations with OAB presence. However, whether baseline inflammatory status predicts response to beta-3 adrenergic agonist therapy remains untested. This prospective observational cohort study evaluates the predictive ability of baseline NLR, PLR, and SII for 3-month treatment response to mirabegron 50 mg in women with OAB.

Read the detailed description

BACKGROUND AND RATIONALE: Overactive bladder (OAB) is a chronic lower urinary tract condition characterized by urinary urgency, usually accompanied by frequency and nocturia, with or without urgency incontinence. Beta-3 adrenoceptor agonists such as mirabegron are an established first-line pharmacological option, yet the individual treatment response varies considerably. Emerging evidence links systemic low-grade inflammation to OAB pathophysiology. Baseline hematological indices derived from the routine complete blood count, such as the neutrophil-to-lymphocyte ratio (NLR), the platelet-to-lymphocyte ratio (PLR), and the systemic immune-inflammation index (SII), may therefore carry predictive information at no additional cost.

STUDY OBJECTIVES: This prospective observational cohort study evaluates whether baseline NLR predicts the clinical response to standard mirabegron therapy (50 mg/day) at 3 months in treatment-naive women with OAB. The discriminative ability of baseline PLR and SII and the adjusted association of NLR with response are evaluated as secondary objectives.

METHODS: Consecutive eligible treatment-naive women in whom mirabegron 50 mg is initiated within routine clinical care are enrolled. Baseline evaluation includes clinical assessment, a 3-day voiding diary, a validated symptom questionnaire, routine urodynamic parameters, and a standardized complete blood count. Inflammatory indices are calculated with standard formulas. Response is assessed at 3 months. Data are collected on standardized case report forms and verified against electronic medical records.

STATISTICAL CONSIDERATIONS: The enrollment target is 115 patients to reach 80 evaluable patients. The discriminative ability of baseline inflammatory indices will be evaluated with ROC curve analysis; multivariable modeling will be used to assess adjusted associations. Details are prespecified in the study protocol.

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Conditions studied

  • Overactive Bladder (OAB)

Keywords

  • Overactive Bladder
  • Adrenergic beta 3 Receptor Agonists
  • Inflammation
  • Biomarkers
  • Blood Cell Counts
  • Neutrophil-to-Lymphocyte Ratio
  • Platelet-to-Lymphocyte Ratio
  • Systemic Immune-Inflammation Index
  • NLR
  • PLR
  • SII
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In context

Urinary Bladder, Overactive

858 studies on the registry are indexed under Urinary Bladder, Overactive; 127 are open to participants now.

This study's planned enrollment of 115 is close to the median of 120 across 169 observational studies indexed under Urinary Bladder, Overactive.

Browse Urinary Bladder, Overactive studies →

Lead sponsor

Bagcilar Training and Research Hospital is the lead sponsor of 55 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Treatment-naive adult women with overactive bladder attending the urogynecology outpatient clinic of a tertiary referral hospital in Istanbul, Turkey, in whom mirabegron 50 mg is initiated within routine clinical care. Consecutive eligible patients are enrolled.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Female patients aged 18 years or older
  • Overactive bladder symptoms for at least 3 months
  • Mirabegron 50 mg planned by physician decision within routine care
  • Ability to provide written

Exclusion criteria

Exclusion Criteria:

  • Any previous OAB-specific treatment other than behavioral therapy (oral antimuscarinic or beta-3 agonist, intravesical botulinum toxin, sacral neuromodulation, or posterior tibial nerve stimulation)
  • Acute infection within the last 4 weeks, including culture-confirmed urinary tract infection
  • Chronic inflammatory disease (rheumatologic or disease, or inflammatory bowel disease)
  • Active or cancer treatment within the last 5 years
  • Use of systemic within the last 4 weeks, or chronic NSAID or use
  • Conditions affecting lower urinary tract function other than OAB (neurogenic bladder, urinary tract stones, history of pelvic radiotherapy or bladder surgery, pelvic organ prolapse stage 3 or higher, or stress-predominant mixed urinary incontinence)
  • Known diagnosis of hematologic disease, anemia (\<9), or disorder (PLT\<100.000 or >600.000)
  • Significant renal or hepatic impairment ( below 30 mL/min/1.73 m2, or class B or C)
  • Uncontrolled hypertension (180/110 mmHg or higher) or any other to mirabegron
  • Pregnancy or lactation
  • Major surgery or trauma within the last 3 months
  • Cognitive or functional inability to complete the voiding diary
Terms in these criteria, in plain language(10)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

Child-Pugh class

A score of how well the liver works in people with liver disease such as cirrhosis: class A is mild, B moderate and C severe.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
115 participants (estimated)
Patient registry
No

Groups and cohorts

  • Treatment-naive OAB cohort

    Treatment-naive adult women with overactive bladder in whom mirabegron 50 mg once daily is initiated by physician decision within routine clinical care. Baseline assessment includes a 3-day voiding diary, the ICIQ-UI SF questionnaire, routine urodynamic evaluation, and a standardized complete blood count; treatment response and global improvement are assessed at 3 months using the ICIQ-UI SF and PGI-I scales.

    Drug: Mirabegron (beta3-adrenoceptor agonist)

Interventions

  • Mirabegron 50 mg orally once daily, initiated and managed by the treating physician as part of routine clinical care. The drug is not assigned by the study protocol; the study observes patients in whom this treatment has been started within standard practice.

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What researchers measure

Primary outcomes

  1. Discriminative ability of baseline neutrophil-to-lymphocyte ratio for mirabegron treatment response

    Treatment response is defined as achieving a minimally clinically important difference (MCID) of a reduction of at least 3 points from baseline in the total International Consultation on Incontinence Questionnaire Urinary Incontinence Short Form (ICIQ-UI SF) score at 3 months, cross-validated by patient-reported improvement on the Patient Global Impression of Improvement (PGI-I) scale (ratings of "very much improved" or "much improved"). The total ICIQ-UI SF score ranges from 0 to 21, with higher scores indicating greater symptom severity and impact on quality of life; a decrease represents clinical improvement. The area under the ROC curve (AUC) of baseline neutrophil-to-lymphocyte ratio for discriminating responders from non-responders is reported with its 95 percent confidence interval.

    Time frame: 3 months

Secondary outcomes

  1. Discriminative ability of baseline platelet-to-lymphocyte ratio for mirabegron treatment response

    The area under the ROC curve of baseline PLR for discriminating responders from non-responders (composite response definition) is reported with its 95 percent confidence interval.

    Time frame: 3 months

  2. Discriminative ability of baseline systemic immune-inflammation index for mirabegron treatment response

    The area under the ROC curve of baseline SII for discriminating responders from non-responders (composite response definition) is reported with its 95 percent confidence interval.

    Time frame: 3 months

  3. Association of baseline NLR with mirabegron treatment response adjusted for clinical covariates

    The adjusted odds ratio and 95 percent confidence interval for baseline NLR are estimated with composite treatment response as the dependent variable.

    Time frame: 3 months

07

Study locations

1 of 1 sites recruiting
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References and documents

Publications

  • Kwon J, Kim DY, Cho KJ, Hashimoto M, Matsuoka K, Kamijo T, Wang Z, Karnup S, Robertson AM, Tyagi P, Yoshimura N. Pathophysiology of Overactive Bladder and Pharmacologic Treatments Including beta3-Adrenoceptor Agonists -Basic Research Perspectives. Int Neurourol J. 2024 Feb;28(Suppl 1):12-33. doi: 10.5213/inj.2448002.001. Epub 2024 Feb 29. PubMed 38461853 ↗
  • Matta R, Saskin R, Neu S, Locke JA, Kowalczyk A, Steup A, Herschorn S. Predicting Mirabegron Treatment Response in Patients with Overactive Bladder: A Post Hoc Analysis of Data from Clinical Trials. Eur Urol Focus. 2023 Nov;9(6):957-965. doi: 10.1016/j.euf.2023.04.001. Epub 2023 Apr 27. PubMed 37120417 ↗
  • Zheng P, Wang X, Ni J. Relationship between the systemic immune-inflammatory index and overactive bladder risk: A cross-sectional assessment involving United States Adults. PLoS One. 2025 May 7;20(5):e0323052. doi: 10.1371/journal.pone.0323052. eCollection 2025. PubMed 40333820 ↗
  • Kim S, Park JH, Oh YH, Kim HJ, Kong MH, Moon J. Correlation between neutrophil to lymphocyte ratio and overactive bladder in South Korean women: a community-based, cross-sectional study. BMJ Open. 2021 Oct 28;11(10):e048309. doi: 10.1136/bmjopen-2020-048309. PubMed 34711592 ↗

Individual participant data

Plan to share: No — Individual participant data will not be shared in order to protect participant privacy and maintain compliance with institutional data protection regulations. De-identified aggregate data that support the findings of this study will be available upon reasonable request from the corresponding author.

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Timeline

2 registry updates since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it movedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Nov 2026 (actual). Primary completion is estimated for Nov 2027, 12 months after the start.

Of 46 non-industry observational studies under Urinary Bladder, Overactive, half reached primary completion within 35 months of starting (the median), counting those still running; a quarter within 17 and three quarters within 50. This study's planned 12 months is below that.

Counting every sponsor, half of 59 studies reached it within 32 months; a quarter within 17 and three quarters within 45.

Start moved twice since we started tracking on Sep 25, 2026: Oct 2026 → Nov 2026, last on Nov 3, 2026.

Primary completion moved twice since we started tracking on Sep 25, 2026: Oct 2027 → Nov 2027, last on Nov 3, 2026.

Earlier changes are on the record history on ClinicalTrials.gov ↗

How these figures are worked out, and which studies are left out of them.

Registered
Aug 15, 2026
First posted
Aug 19, 2026
StartActual
Nov 2, 2026was Oct 2026
Primary completionEst.
Nov 2, 2027was Oct 2027
CompletionEst.
Nov 2, 2027
Last update
Nov 3, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Status
Not yet recruiting→Recruiting
changed Nov 3, 2026
Sites
Bagcilar Training and Research Hospital is now Recruiting
Nov 3, 2026
Start date
Oct 1, 2026→Nov 2, 2026 (actual)
moved 2 times, Oct 5, 2026 – Nov 3, 2026
Primary completion
Oct 1, 2027→Nov 2, 2027
moved 2 times, Oct 5, 2026 – Nov 3, 2026
Study completion
Nov 1, 2027→Nov 2, 2027
Nov 3, 2026
Primary outcomes
1 description edited
What changed in the outcomes
  • DescriptionDiscriminative ability of baseline neutrophil-to-lymphocyte ratio for mirabegron treatment response: how it is measured was reworded
Oct 5, 2026
Show all 2 updates
  1. Nov 3, 2026
    Not yet recruiting→Recruiting
    Bagcilar Training and Research Hospital is now Recruiting
    Start date Nov 1, 2026→Nov 2, 2026 (now actual)
    Primary completion Nov 1, 2027→Nov 2, 2027
    Study completion Nov 1, 2027→Nov 2, 2027
    + 1 other change: verification date
  2. Oct 5, 2026
    Start date Oct 1, 2026→Nov 1, 2026
    Primary completion Oct 1, 2027→Nov 1, 2027
    Primary outcomes 1 description edited
    What changed in the outcomes
    • DescriptionDiscriminative ability of baseline neutrophil-to-lymphocyte ratio for mirabegron treatment response: how it is measured was reworded
    + 2 other changes: verification date and arm descriptions

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

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Registry details

Key details

Study ID
NCT07773532
Lead sponsor
Bagcilar Training and Research Hospital
Responsible party
özgür aslan (Specialist Physician, Bagcilar Training and Research Hospital) — Principal investigator
First posted
Aug 19, 2026
Start date
Nov 2, 2026
Primary completion
Nov 2, 2027 (estimated)
Completion
Nov 2, 2027 (estimated)
Last update
Nov 3, 2026

Study contacts

Özgür Aslan, MD
Contact
ozgraslan92@gmail.com
+90 5384243325
Özgür Aslan, MD
principal investigator · Bagcilar Training and Research Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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