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Recruiting NCT07495072

Early vs Delayed Intravesical Blad-Care During BCG Therapy

No phase Interventional Urinary Bladder Neoplasms BCG-Induced Cystitis

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: Hyaluronic Acid and Chondroitin Sulfate (Blad-Care™).
Who it may be relevant to
Registry conditions: Urinary Bladder Neoplasms, BCG-Induced Cystitis. Basic parameters: from 19 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
South Korea
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

Optimal Timing of Intravesical GAG Restoration Therapy for BCG-Induced Bladder Toxicity in Patients With Non-Muscle-Invasive Bladder Cancer: A Prospective Randomized Study

Overview

Intravesical Bacillus Calmette-Guérin (BCG) therapy is the standard adjuvant treatment for patients with intermediate- and high-risk non-muscle-invasive bladder cancer (NMIBC). However, BCG therapy frequently induces local bladder irritation symptoms including urinary frequency, urgency, dysuria, hematuria, and suprapubic pain, which may reduce quality of life and lead to treatment interruption. Blad-Care™ is an intravesical therapy containing hyaluronic acid and chondroitin sulfate, key components of the urothelial glycosaminoglycan (GAG) layer. Restoration of the GAG layer may protect the bladder mucosa and reduce inflammation-induced bladder irritation symptoms. This prospective randomized study aims to determine whether early administration of intravesical Blad-Care during BCG induction improves BCG-induced bladder toxicity compared with delayed administration after completion of BCG induction therapy.

Detailed description

Non-muscle-invasive bladder cancer (NMIBC) accounts for approximately 70-75% of newly diagnosed bladder cancers. Intravesical BCG therapy after transurethral resection of bladder tumor (TURBT) significantly reduces tumor recurrence and progression in intermediate- and high-risk NMIBC.

Despite its proven oncologic benefit, BCG therapy commonly induces local bladder inflammation resulting in urinary frequency, urgency, dysuria, hematuria, and suprapubic pain. These adverse effects may impair patient quality of life and reduce adherence to BCG therapy.

Experimental evidence suggests that BCG-induced cystitis is associated with damage to the urothelial glycosaminoglycan (GAG) layer, which normally protects the bladder mucosa from urinary irritants. Disruption of this protective barrier may contribute to bladder irritation symptoms.

Blad-Care™ contains hyaluronic acid and chondroitin sulfate, two major components of the GAG layer, and may restore the urothelial protective barrier and reduce bladder inflammation.

Previous studies have suggested that GAG restoration therapy may improve symptoms in patients with chemical cystitis; however, evidence regarding its role during BCG therapy remains limited, and the optimal timing of administration has not been established.

This multicenter prospective randomized study will compare early versus delayed intravesical administration of Blad-Care during BCG induction in patients with NMIBC to determine the optimal timing for reducing BCG-induced bladder toxicity.

Interventions

  • Drug Hyaluronic Acid and Chondroitin Sulfate (Blad-Care™)
    Intravesical instillation of a sterile solution containing sodium hyaluronate and chondroitin sulfate designed to restore the urothelial glycosaminoglycan (GAG) layer.

Primary outcome measures

  • Change from baseline in the combined Interstitial Cystitis Symptom Index (ICSI) and Interstitial Cystitis Problem Index (ICPI) score [Time frame: Baseline (Week 0), after 3rd BCG instillation (Week 3), after 6th BCG instillation (Week 6), and 2 months after completion of BCG therapy (Week 14).]
Secondary outcome measures (6)
  • Change from Baseline in Visual Analogue Scale (VAS) Score for Suprapubic Pain [Time frame: Baseline (Week 0), after 3rd BCG instillation (Week 3), after 6th BCG instillation (Week 6), and 2 months after completion of BCG therapy (Week 14).]
  • Incidence and Severity of Hematuria [Time frame: From the first BCG instillation (Week 1) through 2 months after completion of BCG therapy (Week 14).]
  • Incidence of Treatment-Emergent Adverse Events (TEAEs) [Time frame: From the first BCG instillation (Week 1) through 2 months after completion of BCG therapy (Week 14).]
  • BCG Treatment Completion Rate [Time frame: From the date of the first BCG instillation (Week 1) through the date of the sixth BCG instillation (Week 6).]
  • Incidence of Initiation of Additional Medications for Lower Urinary Tract Symptoms (LUTS) [Time frame: From the first BCG instillation (Week 1) through 2 months after completion of BCG therapy (Week 14).]
  • Recurrence-Free Rate of Non-Muscle Invasive Bladder Cancer (NMIBC) [Time frame: From the date of randomization until the study completion (June 2027, approximately 15 months).]

Eligibility criteria

Inclusion criteria

  • Adults aged ≥19 years
  • Histologically confirmed non-muscle-invasive bladder cancer
  • Candidates for intravesical BCG therapy
  • Negative urine culture prior to BCG therapy
  • Ability to provide written informed consent

Exclusion criteria

  • Hypersensitivity to components of Blad-Care
  • Contraindication to BCG therapy
  • Neurogenic bladder or significant urinary tract abnormalities
  • Severe renal dysfunction
  • Any condition considered unsuitable for study participation by the investigator

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

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Supportive care

Study locations

South Korea · 1 center
  • Kyung Hee University Hospital — Seoul

Identifiers

NCT: NCT07495072 · EMC-KHMC-URO-2025 · KHUH 2025-11-064-002

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗