Real-Time (TRUS) Guidance in Endoscopic Treatment of BPH
ConditionBPH (Benign Prostatic Hyperplasia)
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age50-80
SponsorAssiut University
About this trial
The study aims to evaluate the role of TRUS in improving the efficacy and safety of endoscopic enucleation of prostate and TURP.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Male patients aged 50-80 years
Diagnosed with benign prostatic hyperplasia (BPH) and scheduled for TURP or prostatic adenoma enucleation.
The patients have clear indication for endoscopic surgery (according to the guidelines).
Clinically fit patients for surgery.
Disqualifiers
• Prostate cancer
Previous urethral or prostate surgery
Neurogenic bladder
Urethral stricture
Trial design
Design model
Parallel
Treatments tested in this trial
TRUS-Guided TURP and enucleation
Procedure/Surgeryrealtime TRUS guidance during the procedure (TURP and enucleation)
Standard TURP and enucleation
Procedure/SurgeryNo TRUS guidance during the procedure (TURP and enucleation)
Treatment groups
114 Participants
are divided into 2 treatment groupsGroup A: Control groupExperimental treatment 1 intervention
Group B: TRUS Guided groupExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
efficacy of endoscopic treatment of BPH
Intervention efficacy will be evaluated by comparing the Peak flow rate in ml/second.(measured by uroflowmetry) between the two groups
Time frame
At 12 weeks after the procedureSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: