Association Between Qmax/eGFR Ratio and LUTS Severity in Men Over 40
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Lower Urinary Tract Symptom, Voiding Dysfunction, Male Urological Health, Renal Function. Basic parameters: from 40 years · Male.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
The Role of Qmax/eGFR Ratio in Assessing Symptom Severity and QoL in Men Over 40 With LUTS
Overview
This study will look at how well a measure called the Qmax/eGFR ratio is related to the severity of urination problems in men over the age of 40. Qmax is a test that shows how fast a person can urinate, and eGFR is a number that reflects kidney function. Men who have urinary symptoms will be asked to do a urine flow test, a blood test, and fill out a questionnaire about their symptoms and quality of life. We will study if there is a link between the Qmax/eGFR ratio and how severe their symptoms are. The results may help doctors better understand how kidney and urinary function are related in men with these problems.
Detailed description
This prospective observational study aims to explore the clinical relevance of the Qmax/eGFR ratio in men over 40 years of age presenting with lower urinary tract symptoms (LUTS). Qmax, derived from uroflowmetry, reflects bladder emptying function, while eGFR represents renal filtration capacity. While both parameters are routinely measured in clinical practice, their combined predictive or associative value in LUTS severity has not been well defined.
Participants will undergo standard non-invasive assessments including uroflowmetry, serum creatinine testing (for eGFR calculation), and will complete the International Prostate Symptom Score (IPSS) questionnaire. The IPSS includes both total symptom score and quality of life (QoL) component. The primary objective is to evaluate the correlation between the Qmax/eGFR ratio and IPSS total score. Secondary objectives include the relationship between Qmax/eGFR and QoL scores, as well as analysis based on prostate volume categories.
This study seeks to identify whether the Qmax/eGFR ratio may serve as a composite marker reflecting both voiding efficiency and renal function in the clinical assessment of LUTS, potentially supporting more individualized decision-making in urological practice.
Primary outcome measures
- Correlation Between Qmax/eGFR Ratio and Total IPSS Score [Time frame: At baseline]
- Correlation Between Qmax/eGFR Ratio and IPSS Quality of Life Subscore [Time frame: At baseline]
Secondary outcome measures (2)
- Factors Associated With Qmax/eGFR Ratio [Time frame: At baseline]
- Association of Clinical Variables With Qmax/eGFR Ratio [Time frame: At baseline]
Eligibility criteria
Inclusion criteria
- Male patients aged 40 years or older presenting with lower urinary tract symptoms (LUTS)
- Able to provide informed consent
- Willing and able to undergo uroflowmetry and blood testing
- Able to complete the IPSS questionnaire, including the QoL item
- Estimated glomerular filtration rate (eGFR) ≥ 30 mL/min/1.73m²
Exclusion criteria
- History of urological surgery (e.g., prostatectomy, bladder surgery)
- Diagnosed or suspected prostate cancer
- Active urinary tract infection (based on clinical symptoms or urinalysis)
- Neurological conditions affecting bladder function (e.g., Parkinson's disease, spinal cord injury)
- Presence of an indwelling urinary catheter at enrollment
- eGFR < 30 mL/min/1.73m²
- Inability to perform uroflowmetry or complete clinical evaluations
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07055425 · MAR.UAD.0024