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Influence of Hyaluronic Acid on Bacillus Calmette-Guérin Local Side Effects

Primary Purpose

Poisoning by BCG Vaccine

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Hyaluronic Acid
BCG (Immucist®)
Sponsored by
University of Rome Tor Vergata
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Poisoning by BCG Vaccine focused on measuring BCG, hyaluronic acid, non-muscle invasive bladder cancer, non bacterial cystitis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Histologically proven non-muscle invasive bladder cancer;
  • Indication to intravesical instillation of BCG according to EAU guidelines;
  • Age > 18 years;
  • Willingness, to participate to the study;
  • Written informed consent.

Exclusion Criteria:

  • Previous or ongoing BCG or different intravesical instillations;
  • Urinary tract infections (UTI) or other known pathologies of the lower urinary tract;
  • Indication for a radical cystectomy;
  • Severe systemic disorders, including neurological pathologies, kidney, liver or heart failure;
  • Contraindications to BCG use.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    BCG alone (Immucist®)

    Hyaluronic acid

    Arm Description

    Group A receive BCG (Immucist® 81 mg, Sanofi-Aventis Group) alone

    Group B receive BCG and HA 40 mg (Cystistat, Mylan, Pittsburgh, PA, U.S.A.).

    Outcomes

    Primary Outcome Measures

    Visual Analogue Scale for Pain
    1 to 10 scale (1 minimum pain perceivable; 10 unbearable pain, as perceived by the patient)

    Secondary Outcome Measures

    Full Information

    First Posted
    July 31, 2014
    Last Updated
    May 26, 2015
    Sponsor
    University of Rome Tor Vergata
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02207608
    Brief Title
    Influence of Hyaluronic Acid on Bacillus Calmette-Guérin Local Side Effects
    Official Title
    Pilot Study of Influence of Hyaluronic Acid (HA) on Bacillus Calmette-Guérin (BCG) Local Side Effects
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2015
    Overall Recruitment Status
    Completed
    Study Start Date
    September 2011 (undefined)
    Primary Completion Date
    August 2012 (Actual)
    Study Completion Date
    August 2012 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Rome Tor Vergata

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of this study is to evaluate a possible role of intravesical Hyaluronic Acid in reducing local toxicity of Bacillus Calmette Guerin (BCG) used to treat bladder urothelial cell carcinoma.
    Detailed Description
    Bacillus Calmette-Guérin (BCG) is considered the most effective treatment to increase disease-free interval and reduce progression of non-muscle invasive bladder cancer (NMIBC) [1]. Although considered safe, BCG can produce both local and systemic side effects leading to treatment discontinuation or interruption. The most common local side-effects of BCG intravesical instillations include cystitis, characterized by irritative voiding symptoms and hematuria, which occur in approximately 75% of all patients. More rarely, serious local adverse events as a result of BCG infection, such as symptomatic granulomatous prostatitis and epididymo-orchitis, might occur and require permanent discontinuation of BCG treatment. Systemic side-effects include flu-like symptoms, such as general malaise and fever, occuring in approximately 40% of patients. A high persistent fever might be related to BCG infection or sepsis. Local and systemic side-effects might lead to discontinue intravesical BCG treatment in approximately 20% of patients [2]. Up to 54% of the patients undergoing intravesical therapy with chemotherapeutic agents to treat superficial bladder tumours can be affected by nonbacterial cystitis [3]. Several solutions have been proposed to reduce the occurrence of side effects from BCG with the aim to limit BCG discontinuation and the concomitant discomfort during endovesical treatment. Some Authors have proposed to avoid BCG administration in case of TUR within previous 2 weeks, traumatic catheterization, macroscopic hematuria, urethral stenosis, active tuberculosis, prior Bacillus Calmette-Guérin sepsis, immuno-suppression or urinary tract infection [4]. Other procedures include the prophylactic administration of isoniazid [5] or ofloxacin [6,7] or usually involve BCG dose reductions [8]. In common practice antimicrobials, anticholinergics, anaesthetics and analgesics are often used to relieve patients' symptoms. Glycosaminoglycan (GAG) substitution therapy is an emerging treatment of Bladder Pain Syndrome/Interstitial Cystitis (BPS/IC) and response rates between 30% and 80% have been described with intravesical administration of various GAGs (hyaluronic acid, pentosan polysulfate, heparin, chondroitin sulfate, and dimethyl sulfoxide) [9,10]. Few papers report the results of GAG substitution therapy in the treatment of radiation and chemical cystitis [9,10]. To our knowledge, to date, only two papers have described GAG use in the treatment of BCG local side effects; this papers show very good results, with significant reduction of lower urinary tract symptoms after intravesical administration of HA [11,12]. Aim of the present randomized pilot study was to evaluate if the sequential administration of HA and BCG could be safe in prevention of early recurrence and progression of bladder tumor, and safe in reduction of local side-effects in patients with high risk NMIBC.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Poisoning by BCG Vaccine
    Keywords
    BCG, hyaluronic acid, non-muscle invasive bladder cancer, non bacterial cystitis

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    30 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    BCG alone (Immucist®)
    Arm Type
    Active Comparator
    Arm Description
    Group A receive BCG (Immucist® 81 mg, Sanofi-Aventis Group) alone
    Arm Title
    Hyaluronic acid
    Arm Type
    Experimental
    Arm Description
    Group B receive BCG and HA 40 mg (Cystistat, Mylan, Pittsburgh, PA, U.S.A.).
    Intervention Type
    Drug
    Intervention Name(s)
    Hyaluronic Acid
    Other Intervention Name(s)
    Cystistat (Mylan, Pittsburgh, PA, U.S.A.)
    Intervention Description
    Add hyaluronic acid to BCG Treatment
    Intervention Type
    Drug
    Intervention Name(s)
    BCG (Immucist®)
    Other Intervention Name(s)
    BCG
    Intervention Description
    Usual BCG treatment
    Primary Outcome Measure Information:
    Title
    Visual Analogue Scale for Pain
    Description
    1 to 10 scale (1 minimum pain perceivable; 10 unbearable pain, as perceived by the patient)
    Time Frame
    Before and after six weeks of treatment (end of induction course)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Histologically proven non-muscle invasive bladder cancer; Indication to intravesical instillation of BCG according to EAU guidelines; Age > 18 years; Willingness, to participate to the study; Written informed consent. Exclusion Criteria: Previous or ongoing BCG or different intravesical instillations; Urinary tract infections (UTI) or other known pathologies of the lower urinary tract; Indication for a radical cystectomy; Severe systemic disorders, including neurological pathologies, kidney, liver or heart failure; Contraindications to BCG use.

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    25123116
    Citation
    Topazio L, Miano R, Maurelli V, Gaziev G, Gacci M, Iacovelli V, Finazzi-Agro E. Could hyaluronic acid (HA) reduce Bacillus Calmette-Guerin (BCG) local side effects? Results of a pilot study. BMC Urol. 2014 Aug 13;14:64. doi: 10.1186/1471-2490-14-64.
    Results Reference
    derived

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    Influence of Hyaluronic Acid on Bacillus Calmette-Guérin Local Side Effects

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