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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03038321
Other study ID # R/17.01.02
Secondary ID
Status Active, not recruiting
Phase Phase 4
First received January 15, 2017
Last updated May 19, 2017
Start date February 1, 2017
Est. completion date December 2019

Study information

Verified date March 2017
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Compare the different supposed clinical treatment of side effects associated with intravesical BCG by levofloxacin (quinolones) vs solifenacin (selective anti-muscarinic) vs lornoxicam (NSAID)


Description:

For urothelial carcinoma (UC), which accounts for over 90% of bladder cancers, more than 70% of bladder cancer patients present with non‐muscle‐invasive disease. Approximately 40-80% of these tumors will recur within the first year, of which 10-25% will progress to muscle‐invasive disease.

Intravesical treatments with cytotoxic chemotherapy and immunotherapy have become the mainstay following transurethral resection (TUR). Increasing knowledge of BCG use allows for effective management of these once debilitating side effects. The majority of patients will still experience cystitis‐like symptoms to some degree, including urinary frequency (71%), cystitis (67%), fever (25%), and hematuria (23%).

Oxybutynin increases in fever, flu-like symptoms, dry mouth and constipation. However, in this study oxybutynin started the night before treatment causing an element of incomplete bladder emptying and allowing an increased BCG dwell time. We think that these effect can be reversed by use anticholinergic 6 hours post BCG instillation Anti-inflammatory drugs significantly reduced BCG-induced granulocyte activation and did not impair BCG-induced lymphocyte cytotoxicity against bladder tumor cells in mice. The committee of International Bladder Cancer Group (IBCG) recommend use of anti-inflammatory agents (NSAIDs) for treatment of non-bacterial or chemical cystitis and other systemic BCG side effect.

Fluoroquinolone with tuberculostatic properties, has been shown to significantly prolong survival in mice with BCG systemic infection and did not affect the antitumor efficacy of BCG. ofloxacin significantly decreased by 18.5% the incidence of class II or higher moderate and severe adverse events of BCG.

Because of sparse published studies on BCG side effect management, the 2016 European Association of Urology (EAU) guidelines management options for side effects associated with intravesical BCG modify the IBCG committee clinical practice without any degree of recommendation. So, in this study the investigators will try to fill the gap in the literature.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 150
Est. completion date December 2019
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

• Patients classified as intermediate or high risk of the bladder tumour

Exclusion Criteria:

- Patient over 80 years (natural decline in immune system function)

- Refuse to complete study requirements

- Contraindication to BCG therapy

- High post-void residual (PVR) above 85 ml

- American Urological Association (AUA) Symptoms score above 20

- Sensitivity to previously mentioned 3 drugs

- High serum creatinine

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
sofenacin
solifenacin 10 mg, 6 hours after IVI of BCG and continue for another 2 days post instillation
Tavanic
levofloxacin 500 mg, 6 hours after IVI of BCG and continue for another 2 days post instillation.
Xefo
lornoxicam 8 mg, 6 hours after IVI of BCG and continue for another 2 days post instillation.

Locations

Country Name City State
Egypt Urology and Nephrology Center Mansoura Aldakahlia

Sponsors (1)

Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparing the drugs efficacy on decreasing systemic and local side effects of BCG __ Outcome Measure by Four-class classification grid of BCG adverse events 6 weeks
Secondary Comparing the drugs effect on decreasing voiding and storage urinary symptoms of BCG __ Outcome Measure by overactive bladder symptoms scores and American Urological Association Symptom Index 6 weeks
Secondary Prostatic specific antigen (PSA) change __ Outcome Measure by PSA measure 1 and 3 months post instillation 1 month and 3 months
Secondary recurrence free survival __ Outcome Measure by Number of patients surviving for one year without tumor recurrence will be counted and compared 1 year
See also
  Status Clinical Trial Phase
Recruiting NCT06186414 - A Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of SIM0237 Alone or in Combination With BCG in NMIBC Phase 1
Recruiting NCT06351904 - A Study of RAG-01 in Patients With Non-muscle-invasive Bladder Cancer (NMIBC) Who Have Failed Bacillus Calmette Guérin (BCG) Therapy Phase 1