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Not yet recruiting NCT07513363

The Role of Urinary RhoA, NGF, and BDNF Levels in Overactive Bladder and Vitamin D Deficiency

No phase Interventional Overactive Bladder Vitamin D Deficiency

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
The protocol lists: Urotherapy.
Who it may be relevant to
Registry conditions: Overactive Bladder, Vitamin D Deficiency. Basic parameters: up to 18 years · All.
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
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Role of Urinary RhoA, NGF, and BDNF Levels in Diagnosis and Follow-up in Children With Overactive Bladder and Vitamin D Deficiency.

Overview

The primary aim of this study is to evaluate the role of three specific urinary proteins-RhoA, Nerve Growth Factor (NGF), and Brain-Derived Neurotrophic Factor (BDNF)-as potential biomarkers for the diagnosis and follow-up of children aged 4-18 diagnosed with Overactive Bladder (OAB) and Vitamin D deficiency.

Interventions

  • Behavioral Urotherapy
    Diagnosis and first-line treatment (urotherapy) will be conducted per European Association of Urology (EAU) guidelines.

Primary outcome measures

  • Changes in Urinary Biomarker Levels: * Quantitative measurement of urinary RhoA, NGF (Nerve Growth Factor), and BDNF (Brain-Derived Neurotrophic Factor) levels using the ELISA method. [Time frame: One year]
Secondary outcome measures (1)
  • Clinical Symptom Improvement: * Reduction in LUTS (Lower Urinary Tract Symptoms) based on standardized voiding dysfunction symptom scores. [Time frame: One year]

Eligibility criteria

Inclusion criteria

  • Children aged 4-18 years presenting with active OAB symptoms (frequency, urgency)

Exclusion criteria

  • Neurological diseases
  • Malignancy
  • Active urinary tract infections
  • Anatomical bladder anomalies
  • History of prior OAB treatment/urological surgery.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Diagnostic

Study locations

Turkey (Türkiye) · 1 center
  • Marmara University School of Medicine Urology Department — Pendik

Identifiers

NCT: NCT07513363 · MAR.UAD.0031

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗