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Comparison Study of Narrow Band Imaging Versus White Light Resection in Patients With Bladder Tumors/Cancer

Primary Purpose

Bladder Cancer

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
White Light
Narrow Band Imaging
Sponsored by
Clinical Research Office of the Endourological Society
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bladder Cancer focused on measuring Bladder Cancer, Urothelial carcinoma, Stage pTa or pT1, NMIBC Ta/T1, Narrow Band Imaging, White Light Cystoscopy, Transurethral resection, Superficial bladder tumor, Positive urine cytology

Eligibility Criteria

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

Inclusion Criteria:

  • Patients scheduled for treatment of primary or recurrent non-muscle invasive bladder cancer
  • Patients greater than 18 years of age
  • No tumors in the upper tract (kidneys or ureters)
  • No previous pelvic radiation

Exclusion Criteria:

  • Gross hematuria at the time of resection making visualization with NBI not possible
  • Participation in other clinical studies with investigations drugs concurrently or within 30 days.
  • Pregnancy
  • Conditions associated with a risk of poor compliance or unwilling to follow up

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Other

    Other

    Arm Label

    Narrow Band Imaging

    White Light Trans Urethral Resection

    Arm Description

    Narrow Band Imaging (NBI)

    White Light Trans Urethral Resection

    Outcomes

    Primary Outcome Measures

    Number of Participants With Recurrence and Recurrence Rate at 1 Year Following Narrow Band Imaging and TURB (Arm A) Versus White Light Trans Urethral Resection of Bladder Cancer (TURB) (Arm B) in Patients With Non Muscle Invasive (pTa/T1) Bladder Cancer.
    The primary outcome measure was recurrence rate at 1 year. A recurrence was defined as the new occurrence of a bladder cancer at the same site as or at a different site from the index cancer.

    Secondary Outcome Measures

    Number of Participants With Persistence/Recurrence of Tumors at First 3 Month Follow up After NBI Versus WL Cystoscopy and Tumor Resection
    Peri-operative Morbidity (30 Days) of TURB Between NBI and WL Resection Using the Clavien System.
    Grade I Any deviation from the normal postoperative course without the need for pharmacological treatment or surgical, endoscopic and radiological interventions. Grade II Requiring pharmacological treatment with drugs other than those allowed for grade I complications. Blood transfusions and total parenteral nutrition are also included. Grade III Requiring surgical, endoscopic or radiological intervention Grade III-a Intervention not under general anaesthesia Grade III-b Intervention under general anaesthesia Grade IV Life-threatening complication (including CNS complications: brain haemorrhage, ischaemic stroke, subarachnoid bleeding, but excluding transient ischaemic attacks) requiring IC/ICU management Grade IV-a Single organ dysfunction (including dialysis) Grade IV-b Multi-organ dysfunction Grade V Death of a patient
    Risk Factors for the Development of Peri-operative Morbidity After Instrumental Treatment.
    We looked at different perioperative complications in order to discover peri-operative morbidity after instrumental treatment. The following variables were analyzed: Bleeding, Fever, UTI, Bladder cramps, DVT, CVA/TIA, Lung embolism, Sepsis, Acute Abdomen, and Other perioperative complications.
    Recurrence Rate Related to Additional Treatment Following TURB.

    Full Information

    First Posted
    August 10, 2010
    Last Updated
    March 27, 2018
    Sponsor
    Clinical Research Office of the Endourological Society
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01180478
    Brief Title
    Comparison Study of Narrow Band Imaging Versus White Light Resection in Patients With Bladder Tumors/Cancer
    Official Title
    A Multi-center, International Study to Compare Use of Narrow Band Imaging (NBI) Versus White Light(WL) During Transurethral Resection of Bladder Tumors (TURB) to Asses Recurrence of Bladder Cancer in Terms of Safety and Efficacy
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    August 2010 (undefined)
    Primary Completion Date
    November 2013 (Actual)
    Study Completion Date
    November 2013 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Clinical Research Office of the Endourological Society

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of this study is to compare the recurrence rate at 1 year following Narrow Band Imaging and trans-urethral resection of bladder tumor with White Light and TURB in patients with non-muscle invasive bladder cancer.
    Detailed Description
    Currently bladder tumors are diagnosed visually with standard cystoscopy that uses white light, or light that is generated encompassing the entire visual spectrum. Some tumors such as carcinoma in situ may not be visible using white light and require patients to undergo random bladder biopsies in order to find the cancer. Recently the development of photodynamic agents have been shown to enhance these procedures to accomplish better resection and identify over-looked tumors. However, these methods often require the instillation of dyes into the bladder as well as specialized cystoscopes. Narrow band imaging (NBI) is now available which uses a special filter to limit the light to only certain wavelengths which allows the identification of areas of increased vascularity or abnormalities without the need for dyes. NBI has been investigated in gastro-intestinal disease and found to be beneficial. Early reports in urology suggest that this technology may reduce the number of tumors that are missed which could impact the recurrence rate of bladder tumors, but this is not known at this time.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Bladder Cancer
    Keywords
    Bladder Cancer, Urothelial carcinoma, Stage pTa or pT1, NMIBC Ta/T1, Narrow Band Imaging, White Light Cystoscopy, Transurethral resection, Superficial bladder tumor, Positive urine cytology

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    965 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Narrow Band Imaging
    Arm Type
    Other
    Arm Description
    Narrow Band Imaging (NBI)
    Arm Title
    White Light Trans Urethral Resection
    Arm Type
    Other
    Arm Description
    White Light Trans Urethral Resection
    Intervention Type
    Device
    Intervention Name(s)
    White Light
    Intervention Description
    White Light Cystoscopy
    Intervention Type
    Device
    Intervention Name(s)
    Narrow Band Imaging
    Intervention Description
    Narrow Band Imaging
    Primary Outcome Measure Information:
    Title
    Number of Participants With Recurrence and Recurrence Rate at 1 Year Following Narrow Band Imaging and TURB (Arm A) Versus White Light Trans Urethral Resection of Bladder Cancer (TURB) (Arm B) in Patients With Non Muscle Invasive (pTa/T1) Bladder Cancer.
    Description
    The primary outcome measure was recurrence rate at 1 year. A recurrence was defined as the new occurrence of a bladder cancer at the same site as or at a different site from the index cancer.
    Time Frame
    1 year after treatment
    Secondary Outcome Measure Information:
    Title
    Number of Participants With Persistence/Recurrence of Tumors at First 3 Month Follow up After NBI Versus WL Cystoscopy and Tumor Resection
    Time Frame
    3 months after treatment
    Title
    Peri-operative Morbidity (30 Days) of TURB Between NBI and WL Resection Using the Clavien System.
    Description
    Grade I Any deviation from the normal postoperative course without the need for pharmacological treatment or surgical, endoscopic and radiological interventions. Grade II Requiring pharmacological treatment with drugs other than those allowed for grade I complications. Blood transfusions and total parenteral nutrition are also included. Grade III Requiring surgical, endoscopic or radiological intervention Grade III-a Intervention not under general anaesthesia Grade III-b Intervention under general anaesthesia Grade IV Life-threatening complication (including CNS complications: brain haemorrhage, ischaemic stroke, subarachnoid bleeding, but excluding transient ischaemic attacks) requiring IC/ICU management Grade IV-a Single organ dysfunction (including dialysis) Grade IV-b Multi-organ dysfunction Grade V Death of a patient
    Time Frame
    30 days
    Title
    Risk Factors for the Development of Peri-operative Morbidity After Instrumental Treatment.
    Description
    We looked at different perioperative complications in order to discover peri-operative morbidity after instrumental treatment. The following variables were analyzed: Bleeding, Fever, UTI, Bladder cramps, DVT, CVA/TIA, Lung embolism, Sepsis, Acute Abdomen, and Other perioperative complications.
    Time Frame
    peri-operative
    Title
    Recurrence Rate Related to Additional Treatment Following TURB.
    Time Frame
    Until 135 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients scheduled for treatment of primary or recurrent non-muscle invasive bladder cancer Patients greater than 18 years of age No tumors in the upper tract (kidneys or ureters) No previous pelvic radiation Exclusion Criteria: Gross hematuria at the time of resection making visualization with NBI not possible Participation in other clinical studies with investigations drugs concurrently or within 30 days. Pregnancy Conditions associated with a risk of poor compliance or unwilling to follow up
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jean de la Rosette, MD
    Organizational Affiliation
    AMC University Hospital
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Learn more about this trial

    Comparison Study of Narrow Band Imaging Versus White Light Resection in Patients With Bladder Tumors/Cancer

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