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Solifenacin, Levofloxacin or Lornoxicam, Which Is Ideal for Management of Intravesical Instillation BCG Side Effects?

Primary Purpose

Non-Muscle-invasive Bladder Cancer (NMIBC), Bacillus Calmette-Guerin (BCG) Cystitis, Intra-vesical Instillation

Status
Unknown status
Phase
Phase 4
Locations
Egypt
Study Type
Interventional
Intervention
sofenacin
Tavanic
Xefo
Sponsored by
Mansoura University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Non-Muscle-invasive Bladder Cancer (NMIBC) focused on measuring BCG Cystitis, Bladder Cancer, Levofloxacin, Solifenacin, Lornoxicam

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Urology and Nephrology Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

solifenacin

levofloxacin

lornoxicam

Arm Description

(Sofenacin ''solifenacin 10 m'') [Marcyrl Pharmaceutical Industries - Egypt]

(Tavanic ''levofloxacin 500 mg'') [Sanofi-Aventis - Egypt]

(Xefo ''lornoxicam 8 mg'') [Multi-Apex - Egypt, under license of: NYCOMED, Austria]

Outcomes

Primary Outcome Measures

Comparing the drugs efficacy on decreasing systemic and local side effects of BCG
__ Outcome Measure by Four-class classification grid of BCG adverse events

Secondary Outcome Measures

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
Prostatic specific antigen (PSA) change
__ Outcome Measure by PSA measure 1 and 3 months post instillation
recurrence free survival
__ Outcome Measure by Number of patients surviving for one year without tumor recurrence will be counted and compared

Full Information

First Posted
January 15, 2017
Last Updated
May 19, 2017
Sponsor
Mansoura University
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1. Study Identification

Unique Protocol Identification Number
NCT03038321
Brief Title
Solifenacin, Levofloxacin or Lornoxicam, Which Is Ideal for Management of Intravesical Instillation BCG Side Effects?
Official Title
Solifenacin vs Levofloxacin vs Lornoxicam for Management of Intravesical Instillation of Bacillus Calmette-Guerin (BCG) Side Effects A Single Blinded Randomised Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Unknown status
Study Start Date
February 1, 2017 (Actual)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mansoura University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief 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)
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-Muscle-invasive Bladder Cancer (NMIBC), Bacillus Calmette-Guerin (BCG) Cystitis, Intra-vesical Instillation
Keywords
BCG Cystitis, Bladder Cancer, Levofloxacin, Solifenacin, Lornoxicam

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
150 (Actual)

8. Arms, Groups, and Interventions

Arm Title
solifenacin
Arm Type
Active Comparator
Arm Description
(Sofenacin ''solifenacin 10 m'') [Marcyrl Pharmaceutical Industries - Egypt]
Arm Title
levofloxacin
Arm Type
Active Comparator
Arm Description
(Tavanic ''levofloxacin 500 mg'') [Sanofi-Aventis - Egypt]
Arm Title
lornoxicam
Arm Type
Active Comparator
Arm Description
(Xefo ''lornoxicam 8 mg'') [Multi-Apex - Egypt, under license of: NYCOMED, Austria]
Intervention Type
Drug
Intervention Name(s)
sofenacin
Other Intervention Name(s)
Solfenacin 10 mg
Intervention Description
solifenacin 10 mg, 6 hours after IVI of BCG and continue for another 2 days post instillation
Intervention Type
Drug
Intervention Name(s)
Tavanic
Other Intervention Name(s)
levofloxacin 500
Intervention Description
levofloxacin 500 mg, 6 hours after IVI of BCG and continue for another 2 days post instillation.
Intervention Type
Drug
Intervention Name(s)
Xefo
Other Intervention Name(s)
lornoxicam
Intervention Description
lornoxicam 8 mg, 6 hours after IVI of BCG and continue for another 2 days post instillation.
Primary Outcome Measure Information:
Title
Comparing the drugs efficacy on decreasing systemic and local side effects of BCG
Description
__ Outcome Measure by Four-class classification grid of BCG adverse events
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Comparing the drugs effect on decreasing voiding and storage urinary symptoms of BCG
Description
__ Outcome Measure by overactive bladder symptoms scores and American Urological Association Symptom Index
Time Frame
6 weeks
Title
Prostatic specific antigen (PSA) change
Description
__ Outcome Measure by PSA measure 1 and 3 months post instillation
Time Frame
1 month and 3 months
Title
recurrence free survival
Description
__ Outcome Measure by Number of patients surviving for one year without tumor recurrence will be counted and compared
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hassan Abol-Enein, MD, Phd
Organizational Affiliation
Urology and Nephrology Center
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ahmed Mosbah, MD
Organizational Affiliation
Urology and Nephrology Center
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ahmed Elhussein, MBBCH
Organizational Affiliation
Urology and Nephrology Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ahmed Elkarta, MBBCH
Organizational Affiliation
Urology and Nephrology Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mohamed Soltan
Organizational Affiliation
Urology and Nephrology Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Urology and Nephrology Center
City
Mansoura
State/Province
Aldakahlia
ZIP/Postal Code
35516
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
meta-analyses by contact the Prof. Hassan Abol-Enein, MD, Phd (Study Chair)

Learn more about this trial

Solifenacin, Levofloxacin or Lornoxicam, Which Is Ideal for Management of Intravesical Instillation BCG Side Effects?

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