Urinary CTGF in Benign Prostatic Obstruction

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age40+
SponsorTarik Emre Sener

About this trial

Benign prostatic obstruction (BPO) is one of the most common causes of bladder outlet obstruction (BOO) and may lead to progressive structural and functional alterations in the bladder over time. Prolonged obstruction triggers a bladder remodeling process characterized by detrusor hypertrophy, ischemia-reperfusion injury, smooth muscle loss, and progressive fibrosis. These pathological changes may result in impaired detrusor contractility, increased post-void residual volume, and suboptimal functional recovery following surgical treatment.

Connective tissue growth factor (CTGF) is a matricellular protein that plays a key role in fibrogenesis and is markedly upregulated under hypoxic, ischemia-reperfusion, and inflammatory conditions. Experimental and cellular studies have demonstrated that CTGF promotes fibroblast proliferation, extracellular matrix production, and collagen deposition, thereby contributing to bladder fibrosis. Increased CTGF expression has also been associated with fibrotic differentiation of bladder smooth muscle cells.

The aim of this observational study is to evaluate the relationship between urinary CTGF levels, bladder fibrosis, and functional response to surgical treatment in patients with benign prostatic obstruction. Preoperative urinary CTGF levels will be assessed and correlated with postoperative functional outcomes and clinical improvement. This study aims to determine whether urinary CTGF may serve as a non-invasive biomarker of bladder fibrosis and a potential predictor of surgical treatment response in patients with BPO.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of benign prostatic obstruction (BPO), with or without an indwelling catheter

Patients with an indication for surgical treatment according to EAU guidelines

Disqualifiers

Age < 40 years

Female sex

Prostate-specific antigen (PSA) > 2.5 ng/mL

History of endoscopic urological intervention

Trial population

This study includes male patients older than 40 years with a diagnosis of benign prostatic obstruction (BPO) who have an indication for surgical treatment according to European Association of Urology (EAU) guidelines. Eligible patients may be catheterized or non-catheterized at the time of enrollment. Patients with conditions that may affect bladder function or connective tissue metabolism, including neurological diseases, diabetes mellitus, prior urogenital malignancy or surgery, urethral stricture, or previous pelvic radiotherapy or chemotherapy, are excluded.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • None-placebo

    Other intervention

    No intervention is assigned as part of this observational study. All diagnostic and surgical procedures are performed as part of routine clinical care.

Treatment groups

50 Participants
are divided into 1 treatment group
Group A: Benign Prostatic Obstruction Patients1 intervention

Trial outcomes

Primary outcomes

1

Urinary CTGF Level

Preoperative urinary connective tissue growth factor (CTGF) levels measured to evaluate their association with bladder fibrosis and postoperative functional outcomes.

Time frame
Baseline, measured within 1 week prior to surgical treatment

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Tarik Emre Sener

Lead sponsor

Marmara University

Sponsor institution

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