Assessment Of Bladder Tumors Stage And Grade By Outpatient Flexible Cystoscopy Performed By Urology Resident

NCT ID: NCT03148158

Last Updated: 2018-01-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-01-15

Study Completion Date

2019-06-15

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This will be a prospective trial comparing the perspective gross morphological of bladder tumor assessment done by outpatient flexible cystoscopy performed by resident, inpatient rigid cystoscopy done by senior staff and their prediction of the degree of invasion of bladder tumor plus the prediction of the grade compared with the standard pathological result.

Also, assessment of the patient reported outcomes after both flexible and rigid cystoscopy will be done.

In the long run of the study, the prognostic gross morphology with recurrence, progression and cancer specific survival will be assessed.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Bladder Cancer Flexible Cystoscopy Non-muscle Invasive Bladder Cancer (NMIBC) Pain, Postoperative

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Cystoscopy

Outpatient flexible cystoscopy and inpatient rigid cystoscopy

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Men and women 18 years or older
* Denovo or recurrent NMIBC
* Bladder mass discovered in hematuria investigation
* Willing to share in study

Exclusion Criteria

* inability to cooperate with flexible cystoscopic evaluations
* cystoscopies for other kind of intervention (e.g., removal of a ureteral stent)
* Untreated infections
* Other causes of storage or voiding symptoms as untreated benign prostatic hyperplasia (BPH) or interstitial cystitis
* Unpassable urethral stricture
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Mansoura University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Abdelwahab Hashem

Urology Msc, Oncology fellow at Urology and Nephrology Center, Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Hassan Abol-Enein, MD

Role: STUDY_CHAIR

Urology and Nephrology center

Ahmed Mosbah, MD

Role: STUDY_DIRECTOR

Urology and Nephrology center

Mohamed Abdelbaset, Msc

Role: PRINCIPAL_INVESTIGATOR

Urology and Nephrology Center

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Urology and Nephrology Center

Al Mansurah, Aldakahlia, Egypt

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Abdelwahab R. Hashem, Msc

Role: CONTACT

01069678979 ext. 002

Mohammed H. Zahran, MD

Role: CONTACT

01063338690 ext. 002

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Abdelwahab R. Hashem, Msc

Role: primary

00201069678979

Mohammed H. Zahran, MD

Role: backup

00201063338690

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

F-Cystoscopy NMIBC

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.