Urinary Bladder NeoplasmsNBINCT05611762
Narrow-band Imaging Diagnostic Classification System for Bladder Tumors
An observational study of Urinary Bladder Neoplasms, run by Qilu Hospital of Shandong University (Qingdao) at 1 site in China.
Trial summary
The goal of this observational study is to learn about the morphological characteristics of different bladder lesions under narrow-band imaging(NBI) techniques in All patients requiring cystoscopy and biopsy. The main questions it aims to answer are: 1. Read more about this study
- Who is it for?
- Ages 18 to 75 yearsHealthy volunteers can take part
- Conditions the study is for
- Urinary Bladder Neoplasms
- How many people
- 1,064 participants
- Where
- 1 siteChina
- Study dates
- 1 Jan 2021to Dec 2024
- How long will I take part?
- 8 Days
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 75 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: The subject population of this study was patients who required cystoscopy for definitive diagnosis due to hematuria or bladder occupancy; or patients who were routinely reviewed by cystoscopy after elective urinary bladder tumor resection (TURBT). They are all patients who come to our hospital for examination or re-examination.
Who may be able to join
- Age between 18 and 75 years old.
- Patients who require cystoscopy for definitive diagnosis due to hematuria or bladder occupancy; or patients who are routinely reviewed by cystoscopy after electrodesiccation of urinary bladder tumor (TURBT).
- Subjects were able to understand the study content and sign the informed consent form, and were able to actively cooperate and follow the study procedures.
Who cannot join
- People with coagulation disorders.
- Combined with acute urinary tract infection or postoperative infusion of BCG vaccine.
- Urethral stricture or bladder volume too small to perform cystoscopy.
- Severe cardiopulmonary dysfunction who cannot tolerate local anesthesia surgery.
- Women who are menstruating or more than 3 months pregnant.
Trial locations and contacts
1 site in 1 country.
China1 site, 1 recruiting
- Recruiting
Qilu Hospital of Shandong University (Qingdao)
Qingdao, Shandong, 266000
Jun Chen, PhD, +8618560084873, chenjunxinxiang@163.com
About this study
Official title: Establishment of Narrow-band Imaging Diagnostic Classification System for Bladder Tumors
The goal of this observational study is to learn about the morphological characteristics of different bladder lesions under narrow-band imaging(NBI) techniques in All patients requiring cystoscopy and biopsy. The main questions it aims to answer are:
- To clarify the characteristics of different bladder lesions under NBI and to establish a diagnostic classification system for bladder tumors under NBI based on pathological findings.
- Verify the accuracy of this classification system. Participants will record the morphological characteristics under ordinary white light and NBI during cystoscopy, analyze the pathological characteristics of different tissues corresponding to the NBI characteristics, establish a diagnostic classification system for bladder tumor under NBI using pathological biopsy as the diagnostic standard, and then verify the accuracy of this classification standard through clinical.
Read the detailed description
- Background: Bladder cancer is the most common malignancy of the urinary system in China, and its incidence is increasing year by year. Non-muscle invasive bladder cancer (NMIBC) can mostly be removed in a minimally invasive manner by transurethral resection of bladder tumor (TURBT), which has less impact on the patient's quality of life. In contrast, if the tumor progresses to muscle-invasive bladder cancer, radical cystectomy with urinary diversion is required, and patients need to carry a stoma bag for life, which significantly affects their quality of life. Early detection and early treatment can significantly improve the prognosis of bladder cancer patients. At present, cystoscopy under ordinary white light (WLC) is the main diagnostic method to check early bladder tumor and the presence of recurrence, and it is widely used in clinical practice, but its accuracy still needs to be improved. Therefore, in order to further improve the sensitivity and accuracy of cystoscopy, we need some optical imaging techniques as an adjunct to WLC to improve the visualization of tumors by contrast enhancement.
- Narrow-band Imaging (NBI): NBI is a diagnostic endoscopic illumination technology developed by Olympus corporation and integrated into the camera of the cystoscope. The NBI device filters out the red spectrum from white light, allowing the blue and green spectra to be absorbed by hemoglobin. The different penetration of the two spectra within the bladder mucosa enhances the contrast between vascular tissue and normal bladder mucosa, improving the visualization of tumor neovascularization. The shorter wavelength blue light (415 nm) band enters the superficial layer of the mucosa, making the superficial capillaries brownish-black, and the longer wavelength green light (540 nm) band enters the deeper layer of the mucosa, making the submucosal vessels green. Thus, papillary tumors exhibit brownish-green lesions due to the enhancement of submucosal capillaries and dark brown lesions due to the enhancement of the dense superficial vascular system.
- NBI classification criteria for different tumors: Currently, NBI classification criteria have been established for both laryngeal tumors and intestinal tumors. Clinical practice has confirmed that the sensitivity and specificity of NBI in the diagnosis of laryngeal mucosal lesions are higher than those of WLC. researchers at the Cancer Hospital of the Chinese Academy of Medical Sciences have classified laryngeal lesions into 5 categories from precancerous to cancerous lesions and confirmed through clinical validation that the classification criteria can help identify precancerous lesions and tumors in the larynx at an early stage. The Japanese NBI expert group also proposed a general NBI classification for colorectal tumors in 2014, which classified colorectal lesions into polyps, low-grade intramucosal neoplasia, high-grade intramucosal neoplasia/ superficial mucosal invasive carcinoma, and deep mucosal invasive carcinoma according to their different morphological characteristics under NBI. Although the NBI technique has been clinically applied for more than 20 years, there is no uniform classification standard for the manifestation of different bladder tumors under the NBI pattern, and the microscopic diagnosis mostly relies on the clinician's experience, with the possibility of misdiagnosis and missed diagnosis.
- Purpose of the study: This study plans to develop the NBI classification criteria for bladder lesions by summarizing and analyzing the morphological characteristics of different bladder lesions in the NBI pattern, using the pathological findings as a diagnostic basis, and assessing their sensitivity and specificity in order to guide clinical work for a more standardized and accurate diagnosis of bladder tumors and early recurrence, thus improving patient prognosis.
- Research content: This is a prospective multicenter study, which includes all patients who need to undergo cystoscopy and take biopsies in our center and collaborating units, records the characteristics of performance under ordinary white light and NBI in different parts of the bladder during cystoscopy, analyzes the characteristics of NBI corresponding to different histopathology as the diagnostic criteria, establishes the diagnostic classification standard of bladder tumor NBI, and then verifies the reliability of this classification standard through clinical validation. There are two key issues to be addressed in this project: (1) to clarify the characteristics of different bladder lesions under NBI and establish a bladder tumor NBI diagnostic classification system based on the pathological results; (2) to clinically validate the accuracy of the classification criteria.
- Cystoscopy method: The patient was placed in a lithotomy position, and the surgical area was disinfected with iodophor and covered with towels, and the urethral mucosal surface was anesthetized with 2% lidocaine gel. The morphological characteristics of the mucosa and blood vessels under the microscope were recorded, and tissue biopsy was performed in the suspected lesion area, and the biopsy tissue was stored in 10% formalin solution for pathological examination. All operations were performed by urologists of equal seniority who had undergone systematic training.
- Sample size and establishment of classification method: Starting from January 1, 2021, cases were enrolled in our center and collaborating institutions simultaneously according to the inclusion and exclusion criteria. Because the different characteristics of mucosa and submucosal vessels of different nature of tumors in the NBI pattern were easier to distinguish, the proposed sample size was included in combination with the sample size included in the existing classification criteria of colorectal tumors and laryngeal tumors (n=139, 104) as follows: 100 cases in the no lesion group, 200 cases in the benign lesion group, and 200 cases in the malignant lesion group, and cystoscopy was performed according to the above method. For patients who did not require surgical treatment, the histopathological results of biopsy were used as the diagnostic criteria; for patients whose biopsy pathology suggested malignant bladder tumors and required TURBT or total cystectomy, the postoperative pathological results were used as the diagnostic criteria. According to the pathological results, all patients were divided into three groups: no lesion group, benign lesion group, and malignant lesion group. All pathological results were reported and reviewed by the hospital pathology center. The International Society of Urological Pathology (ISUP) classification standard was used for pathological classification, the WHO 2004 bladder cancer grading system was used for histological grading, and the Union International Control Cancer (UICC) 2017 TNM staging system was used for bladder cancer staging.
- Blind design: The cystoscopy operation was performed by four urologists at each center who were trained and dedicated to the operation, separate from the primary clinician; neither the subject nor the investigator knew the patient number information before complete subject screening and enrollment, and the cystoscopy operator did not know the primary history information and relied only on the microscopic presentation to give the initial diagnosis; blinded data review was used.
- Establishment of NBI diagnostic classification system for bladder tumors: Using the pathological results as the "gold standard", the patients were divided into no lesion group, benign lesion group and malignant lesion group, and analyzed the morphological characteristics of normal mucosa, benign and malignant lesions, focal mucosa and submucosal vessels, respectively, against the cystoscopic WLC and NBI microscopic manifestations, to summarize and establish the diagnostic classification system of bladder tumor NBI.
- Clinical validation of the accuracy of the NBI diagnostic classification criteria for bladder tumors: Sample size calculation: There is no diagnostic classification standard for bladder tumor NBI, referring to the classification standard for colorectal tumor NBI, the diagnostic sensitivity of its lesionless group, benign lesion group and malignant lesion group are 75%, 91%, 35%, the specificity is 96%, 70%, 100%, also the tolerance error are 0.1, requiring one-sided test, α is 0.025, the certainty is 80%. In this phase, it is proposed to initially include a total of 564 patients in accordance with this sample size, according to the inclusion and exclusion criteria, prospectively, combined with the loss of follow-up rate (20%) in each group, according to which the 3 groups need to include at least 211, 127, and 226 study subjects, respectively. After the completion of the first part of the trial, the sample size can be corrected according to the established diagnostic classification criteria for NBI, after the initial estimation of its sensitivity and specificity.
The patients enrolled in the study were analyzed for cystoscopic NBI manifestations and given a preliminary diagnosis according to the diagnostic classification of bladder tumor NBI, also using tissue biopsy or surgical pathology as the "gold standard", and the accuracy of this classification was calculated.
Main evaluation indexes: Sensitivity, Specificity, Area under the ROC curve. Secondary evaluation metrics: Positive Predictive Value (PPV), Negative Predictive Value (NPV), Positive Likelihood Ratio (PLR), Negative Likelihood Ratio (NLR), Accuracy Likelihood Ratio (NLR), Accuracy, and Jouden Index.
- Conditions
- Urinary Bladder Neoplasms
- Keywords
- Urinary Bladder Neoplasms, Narrow-banding Imaging, Diagnosis, Cystoscopy
- Medical subject headings
- Urinary Bladder Neoplasms, Disease
What is being measured
The primary outcome is the main question the study is designed to answer.
Cystoscopic WLC and NBI microscopic manifestations, observation of normal mucosa, benign and malignant lesions, morphological characteristics of focal mucosa and submucosal vessels.
Using the pathological results as the "gold standard", the patients were divided into no lesion group, benign lesion group and malignant lesion group, and the morphological characteristics of normal mucosa, benign and malignant lesions, focal mucosa and submucosa vessels were analyzed against cystoscopic WLC and NBI, respectively, to summarize and establish the classification system of bladder tumor NBI diagnosis.
Measured: Cystoscopy 0 days
Analysis of the accuracy of categorical diagnostic criteria
Including sensitivity, specificity, area under the ROC curve, positive predictive value, negative predictive value, positive likelihood ratio, negative likelihood ratio, accuracy, Jouden index
Measured: One year
Based on pathological diagnosis results, evaluate the number of patients with normal mucosa, benign lesions, malignant tumors, and NBI image characteristics
Pathology results are not only the "gold standard" for grouping, but also for assessing the characteristics of NBI images.
Measured: Follow-up period - 7 days after cystoscopy
Secondary outcomes (1)
Safety observation, adverse event record, combined drug use
Important safety indicators during follow-up
Measured: Screening period - within 7 days prior to cystoscopy,Cystoscopy 0 days,Follow-up period - 1 days,Follow-up period - 7 days after cystoscopy after cystoscopy
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Nov 2022
- Study start1 Jan 2021
- Primary completionDec 2024 (estimated)
- Study completionDec 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Urinary Bladder NeoplasmsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 1,064 participants (estimated)
- Target duration
- 8 Days
Sponsor and investigators
- Lead sponsor
- Qilu Hospital of Shandong University (Qingdao)
- Sponsor type
- University, hospital or other
- Collaborators
- Qilu Hospital of Shandong University, The Second Hospital of Shandong University, Shandong Provincial Hospital, Yantai Yuhuangding Hospital, Qianfoshan Hospital
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05611762
- Sponsor's protocol ID
- KYLL2021010
- Acronym
- NBI
- Status last verified
- Dec 2022
- First submitted
- 28 Oct 2022
- Last updated
- 19 Dec 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 19 Dec 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Establishment of Narrow-band Imaging Diagnostic Classification System for Bladder Tumors
- ClinicalTrials.gov ID
- NCT05611762
- Acronym / sponsor ID
- NBI / KYLL2021010
- Conditions
- Urinary Bladder Neoplasms
- Keywords
- Urinary Bladder Neoplasms, Narrow-banding Imaging, Diagnosis, Cystoscopy
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 1,064 participants (estimated)
- Lead sponsor
- Qilu Hospital of Shandong University (Qingdao)University, hospital or other
- Collaborators
- Qilu Hospital of Shandong University, The Second Hospital of Shandong University, Shandong Provincial Hospital, Yantai Yuhuangding Hospital, Qianfoshan Hospital
- Study start
- 1 Jan 2021 (actual)
- Primary completion
- Dec 2024 (estimated)
- Study completion
- Dec 2024 (estimated)
- First posted
- 10 Nov 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this observational study is to learn about the morphological characteristics of different bladder lesions under narrow-band imaging(NBI) techniques in All patients requiring cystoscopy and biopsy. The main questions it aims to answer are:
- To clarify the characteristics of different bladder lesions under NBI and to establish a diagnostic classification system for bladder tumors under NBI based on pathological findings.
- Verify the accuracy of this classification system. Participants will record the morphological characteristics under ordinary white light and NBI during cystoscopy, analyze the pathological characteristics of different tissues corresponding to the NBI characteristics, establish a diagnostic classification system for bladder tumor under NBI using pathological biopsy as the diagnostic standard, and then verify the accuracy of this classification standard through clinical.
Detailed description
- Background: Bladder cancer is the most common malignancy of the urinary system in China, and its incidence is increasing year by year. Non-muscle invasive bladder cancer (NMIBC) can mostly be removed in a minimally invasive manner by transurethral resection of bladder tumor (TURBT), which has less impact on the patient's quality of life. In contrast, if the tumor progresses to muscle-invasive bladder cancer, radical cystectomy with urinary diversion is required, and patients need to carry a stoma bag for life, which significantly affects their quality of life. Early detection and early treatment can significantly improve the prognosis of bladder cancer patients. At present, cystoscopy under ordinary white light (WLC) is the main diagnostic method to check early bladder tumor and the presence of recurrence, and it is widely used in clinical practice, but its accuracy still needs to be improved. Therefore, in order to further improve the sensitivity and accuracy of cystoscopy, we need some optical imaging techniques as an adjunct to WLC to improve the visualization of tumors by contrast enhancement.
- Narrow-band Imaging (NBI): NBI is a diagnostic endoscopic illumination technology developed by Olympus corporation and integrated into the camera of the cystoscope. The NBI device filters out the red spectrum from white light, allowing the blue and green spectra to be absorbed by hemoglobin. The different penetration of the two spectra within the bladder mucosa enhances the contrast between vascular tissue and normal bladder mucosa, improving the visualization of tumor neovascularization. The shorter wavelength blue light (415 nm) band enters the superficial layer of the mucosa, making the superficial capillaries brownish-black, and the longer wavelength green light (540 nm) band enters the deeper layer of the mucosa, making the submucosal vessels green. Thus, papillary tumors exhibit brownish-green lesions due to the enhancement of submucosal capillaries and dark brown lesions due to the enhancement of the dense superficial vascular system.
- NBI classification criteria for different tumors: Currently, NBI classification criteria have been established for both laryngeal tumors and intestinal tumors. Clinical practice has confirmed that the sensitivity and specificity of NBI in the diagnosis of laryngeal mucosal lesions are higher than those of WLC. researchers at the Cancer Hospital of the Chinese Academy of Medical Sciences have classified laryngeal lesions into 5 categories from precancerous to cancerous lesions and confirmed through clinical validation that the classification criteria can help identify precancerous lesions and tumors in the larynx at an early stage. The Japanese NBI expert group also proposed a general NBI classification for colorectal tumors in 2014, which classified colorectal lesions into polyps, low-grade intramucosal neoplasia, high-grade intramucosal neoplasia/ superficial mucosal invasive carcinoma, and deep mucosal invasive carcinoma according to their different morphological characteristics under NBI. Although the NBI technique has been clinically applied for more than 20 years, there is no uniform classification standard for the manifestation of different bladder tumors under the NBI pattern, and the microscopic diagnosis mostly relies on the clinician's experience, with the possibility of misdiagnosis and missed diagnosis.
- Purpose of the study: This study plans to develop the NBI classification criteria for bladder lesions by summarizing and analyzing the morphological characteristics of different bladder lesions in the NBI pattern, using the pathological findings as a diagnostic basis, and assessing their sensitivity and specificity in order to guide clinical work for a more standardized and accurate diagnosis of bladder tumors and early recurrence, thus improving patient prognosis.
- Research content: This is a prospective multicenter study, which includes all patients who need to undergo cystoscopy and take biopsies in our center and collaborating units, records the characteristics of performance under ordinary white light and NBI in different parts of the bladder during cystoscopy, analyzes the characteristics of NBI corresponding to different histopathology as the diagnostic criteria, establishes the diagnostic classification standard of bladder tumor NBI, and then verifies the reliability of this classification standard through clinical validation. There are two key issues to be addressed in this project: (1) to clarify the characteristics of different bladder lesions under NBI and establish a bladder tumor NBI diagnostic classification system based on the pathological results; (2) to clinically validate the accuracy of the classification criteria.
- Cystoscopy method: The patient was placed in a lithotomy position, and the surgical area was disinfected with iodophor and covered with towels, and the urethral mucosal surface was anesthetized with 2% lidocaine gel. The morphological characteristics of the mucosa and blood vessels under the microscope were recorded, and tissue biopsy was performed in the suspected lesion area, and the biopsy tissue was stored in 10% formalin solution for pathological examination. All operations were performed by urologists of equal seniority who had undergone systematic training.
- Sample size and establishment of classification method: Starting from January 1, 2021, cases were enrolled in our center and collaborating institutions simultaneously according to the inclusion and exclusion criteria. Because the different characteristics of mucosa and submucosal vessels of different nature of tumors in the NBI pattern were easier to distinguish, the proposed sample size was included in combination with the sample size included in the existing classification criteria of colorectal tumors and laryngeal tumors (n=139, 104) as follows: 100 cases in the no lesion group, 200 cases in the benign lesion group, and 200 cases in the malignant lesion group, and cystoscopy was performed according to the above method. For patients who did not require surgical treatment, the histopathological results of biopsy were used as the diagnostic criteria; for patients whose biopsy pathology suggested malignant bladder tumors and required TURBT or total cystectomy, the postoperative pathological results were used as the diagnostic criteria. According to the pathological results, all patients were divided into three groups: no lesion group, benign lesion group, and malignant lesion group. All pathological results were reported and reviewed by the hospital pathology center. The International Society of Urological Pathology (ISUP) classification standard was used for pathological classification, the WHO 2004 bladder cancer grading system was used for histological grading, and the Union International Control Cancer (UICC) 2017 TNM staging system was used for bladder cancer staging.
- Blind design: The cystoscopy operation was performed by four urologists at each center who were trained and dedicated to the operation, separate from the primary clinician; neither the subject nor the investigator knew the patient number information before complete subject screening and enrollment, and the cystoscopy operator did not know the primary history information and relied only on the microscopic presentation to give the initial diagnosis; blinded data review was used.
- Establishment of NBI diagnostic classification system for bladder tumors: Using the pathological results as the "gold standard", the patients were divided into no lesion group, benign lesion group and malignant lesion group, and analyzed the morphological characteristics of normal mucosa, benign and malignant lesions, focal mucosa and submucosal vessels, respectively, against the cystoscopic WLC and NBI microscopic manifestations, to summarize and establish the diagnostic classification system of bladder tumor NBI.
- Clinical validation of the accuracy of the NBI diagnostic classification criteria for bladder tumors: Sample size calculation: There is no diagnostic classification standard for bladder tumor NBI, referring to the classification standard for colorectal tumor NBI, the diagnostic sensitivity of its lesionless group, benign lesion group and malignant lesion group are 75%, 91%, 35%, the specificity is 96%, 70%, 100%, also the tolerance error are 0.1, requiring one-sided test, α is 0.025, the certainty is 80%. In this phase, it is proposed to initially include a total of 564 patients in accordance with this sample size, according to the inclusion and exclusion criteria, prospectively, combined with the loss of follow-up rate (20%) in each group, according to which the 3 groups need to include at least 211, 127, and 226 study subjects, respectively. After the completion of the first part of the trial, the sample size can be corrected according to the established diagnostic classification criteria for NBI, after the initial estimation of its sensitivity and specificity.
The patients enrolled in the study were analyzed for cystoscopic NBI manifestations and given a preliminary diagnosis according to the diagnostic classification of bladder tumor NBI, also using tissue biopsy or surgical pathology as the "gold standard", and the accuracy of this classification was calculated.
Main evaluation indexes: Sensitivity, Specificity, Area under the ROC curve. Secondary evaluation metrics: Positive Predictive Value (PPV), Negative Predictive Value (NPV), Positive Likelihood Ratio (PLR), Negative Likelihood Ratio (NLR), Accuracy Likelihood Ratio (NLR), Accuracy, and Jouden Index.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 8 Days
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- The subject population of this study was patients who required cystoscopy for definitive diagnosis due to hematuria or bladder occupancy; or patients who were routinely reviewed by cystoscopy after elective urinary bladder tumor resection (TURBT). They are all patients who come to our hospital for examination or re-examination.
Key inclusion criteria (3 listed)
- Age between 18 and 75 years old.
- Patients who require cystoscopy for definitive diagnosis due to hematuria or bladder occupancy; or patients who are routinely reviewed by cystoscopy after electrodesiccation of urinary bladder tumor (TURBT).
- Subjects were able to understand the study content and sign the informed consent form, and were able to actively cooperate and follow the study procedures.
Key exclusion criteria (5 listed)
- People with coagulation disorders.
- Combined with acute urinary tract infection or postoperative infusion of BCG vaccine.
- Urethral stricture or bladder volume too small to perform cystoscopy.
- Severe cardiopulmonary dysfunction who cannot tolerate local anesthesia surgery.
- Women who are menstruating or more than 3 months pregnant.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Cystoscopic WLC and NBI microscopic manifestations, observation of normal mucosa, benign and malignant lesions, morphological characteristics of focal mucosa and submucosal vessels.
Time frame: Cystoscopy 0 days
Using the pathological results as the "gold standard", the patients were divided into no lesion group, benign lesion group and malignant lesion group, and the morphological characteristics of normal mucosa, benign and malignant lesions, focal mucosa and submucosa vessels were analyzed against cystoscopic WLC and NBI, respectively, to summarize and establish the classification system of bladder tumor NBI diagnosis.
Analysis of the accuracy of categorical diagnostic criteria
Time frame: One year
Including sensitivity, specificity, area under the ROC curve, positive predictive value, negative predictive value, positive likelihood ratio, negative likelihood ratio, accuracy, Jouden index
Based on pathological diagnosis results, evaluate the number of patients with normal mucosa, benign lesions, malignant tumors, and NBI image characteristics
Time frame: Follow-up period - 7 days after cystoscopy
Pathology results are not only the "gold standard" for grouping, but also for assessing the characteristics of NBI images.
1 secondary outcome
Safety observation, adverse event record, combined drug use
Time frame: Screening period - within 7 days prior to cystoscopy,Cystoscopy 0 days,Follow-up period - 1 days,Follow-up period - 7 days after cystoscopy after cystoscopy
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Dec 2022.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Urinary Bladder Neoplasms, run by Qilu Hospital of Shandong University (Qingdao) at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 19 Dec 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Jun Chen, PhD (+8618560084873, chenjunxinxiang@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Cystoscopic WLC and NBI microscopic manifestations, observation of normal mucosa, benign and malignant lesions, morphological characteristics of focal mucosa and submucosal vessels. (time frame: Cystoscopy 0 days). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Dec 2022.