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Recruiting NCT07733167

Intra-Prostatic Epinephrine Injection in Bipolar Transurethral Resection of Large Prostate: Exploring Its Role in Optimizing Surgical Outcomes

Phase III Interventional Intra-Prostatic Epinephrine Injection in Bipolar Transurethral Resection of Large Prostate

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: TURP, Epinephrine.
Who it may be relevant to
Registry conditions: Intra-Prostatic Epinephrine Injection in Bipolar Transurethral Resection of Large Prostate. Basic parameters: from 40 years · Male.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Intra-Prostatic Epinephrine injection in Bipolar Transurethral resection of large prostate: Exploring Its Role in Optimizing Surgical Outcomes

Interventions

  • Device TURP
    Intra-Prostatic Epinephrine injection in Bipolar Transurethral resection of large prostate
  • Drug Epinephrine
    Intra-Prostatic epinephrine injection in Bipolar Transurethral resection of large prostate

Primary outcome measures

  • Intraoperative blood loss , need of blood transfusion [Time frame: 24h post operative]
Secondary outcome measures (1)
  • Prostate volume , post voiding residual urine [Time frame: 3 months]

Eligibility criteria

Inclusion criteria

  • Indication for Prostate Surgery or Procedure - Patients undergoing transurethral resection of the prostate (TURP)
  • Prostate from 80 to 100 gm
  • Failed medical therapy

Exclusion criteria

  • Uncontrolled Hypertension - Patients with significantly high blood pressure despite medication therapy.
  • Unstable angina, recent myocardial infarction, arrhythmias, or severe heart failure.
  • Significant Coagulopathy - Patients with bleeding disorders or on anticoagulants where excessive vasoconstriction may lead to tissue necrosis or inadequate perfusion
  • Hyperthyroidism, Pheochromocytoma or Endocrine Disorders - Patients with catecholamine-secreting tumors or other conditions that can lead to excessive sympathetic stimulation.
  • Treatment in the last 3 months with 5-alpha reductase inhibitors.
  • Genitourinary cancer, urinary tract lithiasis, and urological surgery within the last 3 months

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Ahmed Abdelraouf Saad — Banhā

Identifiers

NCT: NCT07733167 · ms 20-3-2025

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗