CClinicalTrials.gg
Active, not recruitingNCT06820502Updated Feb 11, 2025

OUTCOMES of SIMULTANEOUS TRANSURETHRAL PROSTATE and BLADDER TUMOR RESECTION VERSUS TRANSURETHRAL BLADDER TUMOR RESECTION in BLADDER TUMOR with BLADDER PROSTATE HYPERPLASIA

An interventional study of Transurethral Resection of Prostate (TURP) and Transurethral Resection Of Bladder Tumor in Bladder Cancer Recurrence, BPH (Benign Prostatic Hyperplasia) and Bladder Cancer, sponsored by Allama Iqbal Medical College. Active, not recruiting at 1 site in Pakistan. Open to male participants aged 40 Years to 65 Years. Per ClinicalTrials.gov, last updated 2025-02-11.

Sponsored by Allama Iqbal Medical College · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 5 months after the study started (first participant enrolled Aug 2024, registered Feb 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
40 Years to 65 Years
Sex
Male
01

Study summary

The rationale of my study is that studies have shown that between 50% and 70% of patients treated with trans-urethral bladder tumor resection (TURBT) alone for NMIBC have recurrence with stage and grade progression in 10% to 15% and because of this theoretical danger of tumor cell implantation, many urologists avoid simultaneous trans-urethral prostate resection (TURP) and TURBT due to fear of implantation of tumor cells in the denuded areas of the resected prostate and prefer to perform a separate procedure for each pathological condition. However, others observed no deleterious effects of simultaneous TURBT and TURP. This unsettled controversy that has spanned almost 4 decades. This study will delineate guidelines for outcome of these procedures in terms of better prognosis for patients.

OBJECTIVE:

The objective of the study is to compare the outcome of simultaneous trans-urethral bladder tumor and prostate resection versus trans-urethral bladder tumor resection alone in bladder tumor with prostate hyperplasia in terms of in terms of recurrence of bladder tumor SUBJECTS AND METHODS Study Design: Randomized controlled trial Settings: Department of Urology, Jinnah Hospital and Allama Iqbal Medical College, Lahore.

Study Population: Patients who will undergo TURP and TURBT at Jinnah Hospital, Lahore will be study population.

Duration of study: 3 months after approval of synopsis. Sampling Technique: Non-Probability / consecutive Sampling Sample Size: Sample size calculated with 80 % power of study and 5 % level of significance Assumed recurrence rate of simultaneous trans-urethral bladder tumor resection with prostate resection (Group A) = 53.6% Assumed recurrence rate of trans-urethral bladder tumor resection alone (Group B) = 86.9% Required sample size of total of 60 patients (30 patients in each group)

SAMPLE SELECTION:

Inclusion Criteria

  • Males aged 40 - 65 year
  • First diagnosis of bladder neoplasm less than 4 cm, confined in urinary bladder
  • Prostate volume ≥ 40 and ≤ 80 ml with normal PSA level and obstructive voiding symptoms Exclusion Criteria

    • Patients with previous prostatic, urethral surgery and urinary bladder surgery like diverticulectomy, ureteric reimplant in urinary bladder
    • Patients with coagulopathy
    • Previous history of heart diseases
    • Diagnosis of prostate cancer
    • Urethral stenosis, previous pelvic irradiation, and neurogenic bladder.
    • Recurrent Bladder Tumor

DATA COLLECTION PROCEDURE:

The study involves 60 male patients diagnosed with bladder carcinoma, meeting inclusion criteria. Informed consent, emphasizing data confidentiality, will be obtained. Patients will be thoroughly examined at Jinnah Hospital Lahore. Preoperative assessment includes medical history, physical examination, digital rectal examination, PSA assay, and IPSS. Patients will be randomly assigned one of two treatments through a computer aided randomization. Patients will be followed with preoperative protocols, and undergo procedures under spinal anesthesia. In group A trans-urethral resection with a resectoscope is employed for both TURBT and TURP. In Group B TURBT, a wire loop electrode through the cystoscope removes bladder tumors in small pieces. TURP involves the resectoscope removing prostate tissue in small fragments, controlled by electrocautery. Post-surgery, complications were dealt with. Tissue fragments are sent to the lab for histopathological analysis. Follow-ups adhere to EAU guidelines, recording recurrence and UTI presence. Histopathology reports follow the 2004 WHO classification. The primary outcome recurrence rate will be noted in 3 months. All the information will be collected in a structured questionnaire.

02

Conditions studied

  • Bladder Cancer Recurrence
  • BPH (Benign Prostatic Hyperplasia)
  • Bladder Cancer
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In context

Urinary Bladder Neoplasms

1,616 studies on the registry are indexed under Urinary Bladder Neoplasms; 421 are open to participants now.

This study's enrollment of 60 is close to the median of 60 across 1,163 interventional studies indexed under Urinary Bladder Neoplasms.

Browse Urinary Bladder Neoplasms studies →

Lead sponsor

Allama Iqbal Medical College is the lead sponsor of 9 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
40 Years to 65 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Inclusion criteria

  • Males aged 40 - 65 year
  • First diagnosis of bladder neoplasm less than 4 cm, confined in urinary bladder
  • Prostate volume > 40 and \< 80 ml with normal PSA level and obstructive voiding symptoms

Exclusion criteria

Exclusion Criteria:

-Patients with previous prostatic, urethral surgery and urinary bladder surgery Iike diverticulectomy, ureteric reimplant in urinary bladder Patients with coagulopathy Previous history of heart diseases Diagnosis of prostate cancer Urethral stenosis, previous pelvic irradiation, and neurogenic bladder. Recurrent Bladder Tumor

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Care provider)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    Patients undergoing TURBT and TURP simultaneously

    Patients undergoing TURBT and TURP simultaneously for Bladder tumour and Benign Prostatic Hyperplexia

    Procedure: Transurethral Resection of Prostate (TURP) · Procedure: Transurethral Resection Of Bladder Tumor

  • Experimental
    Patients undergoing TURBT

    Patients undergoing TURBT only for Bladder Tumour and BPH

    Procedure: Transurethral Resection Of Bladder Tumor

Interventions

  • ProcedureTransurethral Resection of Prostate (TURP)

    TURP: Transurethral resection of the prostate remains the criterion standard therapy for obstructive prostatic hypertrophy and is both the surgical treatment of choice and the standard of care when medication fails. It improves obstructive voiding symptoms and urinary flow rate with success rates ranging from 85 to 90% .

  • ProcedureTransurethral Resection Of Bladder Tumor

    TURBT: Trans-urethral resection of bladder tumor (TURBT), performed endoscopically, is the firstline procedure for diagnosis, staging, and treatment of visible bladder tumors,

06

What researchers measure

Primary outcomes

  1. Bladder Tumor Recurrence

    RECURRENCE OF TUMOUR: Recurrence refers to the return of bladder cancer after initial treatment. It can occur in the remaining bladder tissue (if partial cystectomy was performed), in the area where the bladder was removed or in nearby lymph nodes. Recurrence will be measured through regular follow-up cystoscopies and imaging studies (such as ct scans) as recommended by EAU guidelines. Any suspicious findings will be biopsied and confirmed through histopathology. It will be assessed after three months of surgery.

    Time frame: after 3 months of surgery

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Study locations

1 site
  • Department of Urology and Renal Transplant, Jinnah Hospital Lahore/ Allama Iqbal Medical College
    Lahore, Punjab 54550, Pakistan
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References and documents

Individual participant data

Plan to share: Yes

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 11, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06820502
Lead sponsor
Allama Iqbal Medical College
Responsible party
TOOBA HAMID (Post Graduate Resident, Allama Iqbal Medical College) — Principal investigator
First posted
Feb 11, 2025
Start date
Aug 15, 2024
Primary completion
Dec 31, 2024
Completion
Jan 31, 2025 (estimated)
Last update
Feb 11, 2025

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jan 2025. You cannot join it, but the record below documents what was studied.

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