Benign Prostatic Hyperplasia Clinical Trial
Official title:
The Use of REZUM System in Chinese Male Patients With Lower Urinary Tract Symptom Secondary to Benign Prostate Enlargement
Verified date | June 2021 |
Source | Chinese University of Hong Kong |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Men with enlarged prostates commonly experience lower urinary tract symptoms and may go on to develop complications such as acute urinary retention (AUR). Surgery is the standard treatment option required to remove the enlarged prostates and to rectify such complications. Transurethral resection of prostate (TURP) was first performed over 80 years ago and is still regarded as the "gold standard" for the treatment of benign prostatic enlargement (BPE) in prostates between 30 and 80ml. While TURP results in an improvement in symptoms, perioperative morbidity and long-term complications can include postoperative bleeding, urinary retention, incontinence, urethral strictures, erectile dysfunction, and ejaculatory dysfunction. Rezūm is a system uses water steam energy to remove the particular part of the prostate that enlarges and causes symptoms due to BPH. Rezum involves a radiofrequency (RF) generator system and an endoscopic device that is introduced into the body via the urethra. Radiofrequency energy from the generator will heat up a controlled amount of water inside the system and converting the water into vapour or steam. The thermal energy created outside the body is delivered into the prostate tissue through the tiny needle at the tip of the endoscopic device. Small amount of steam will then be injected into the tissue and energy will be released during the conversion of steam to water. The energy will heat up the prostate tissue and result in gradually removal of the targeted obstructive prostate tissue. The treatment procedure takes approximately 3-7 minutes and can be performed as day surgery. No radiofrequency energy is delivered into the body, other than the prostate. Throughout the procedure normal saline (salty water) is running into the urethra through the scope to help ensure better views and to prevent the urethra from overheating. Voiding symptom will gradually improve after the procedure. From clinical study based in Caucasian population, patients had improved urinary flow rate by on average 50% and also improvement in quality of life scores. The treatment results could last for at least 4 years. However, information regarding the use of Rezum in Chinese and Asian is lacking. This study is proposed to evaluate the efficacy and safety of Rezum in our population.
Status | Terminated |
Enrollment | 3 |
Est. completion date | January 29, 2021 |
Est. primary completion date | January 29, 2021 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 50 Years to 80 Years |
Eligibility | Inclusion Criteria: - Men aged between 50 - 80 years - clinically indicated for surgical treatment Exclusion Criteria: - Patients with active urinary tract infection or in retention of urine - Patients with bleeding disorder or on anti-coagulation - Patients with bladder pathology including bladder stone and bladder cancer - Patients with urethral stricture - Patients with neurogenic bladder and/or sphincter abnormalities - Patients with previous nonpharmacological prostate treatment, Prostate cancer - Fail to give informed consent |
Country | Name | City | State |
---|---|---|---|
Hong Kong | Prince of Wales Hospital | Shatin |
Lead Sponsor | Collaborator |
---|---|
Chinese University of Hong Kong |
Hong Kong,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in International Prostate Symptom Score (IPSS) at 6 months after treatment | IPSS score ranging from 0-35 (the higher the worse) | at baseline, 6 months after study intervention | |
Secondary | Complications rate | Complications rate after study intervention | 30 days after study intervention | |
Secondary | Post-op total score in International Prostate Symptom Score (IPSS) | Change in total score of IPSS, score ranging from 0-35 (the higher the worse) | At 3 months, 6 months and 12 months after study intervention | |
Secondary | Post-op quality of life score | Change in quality of life assessed by change in International Prostate QOL score (ranges from 0 to 6, the higher the worse) | At 3 months, 6 months and 12 months after study intervention | |
Secondary | Post-op International Index of Erectile Function 5 (IIEF-5) score | Change in total score of International Index of Erectile Function 5 score (ranges from 0 to 25) | At 3 months, 6 months and 12 months after study intervention | |
Secondary | Post-op Overactive bladder symptom score (OABSS) score | Change in total score of Overactive Bladder Symptom Score (ranges from 0 - 15, the higher the worse) | At 3 months, 6 months and 12 months after study intervention | |
Secondary | Post-op pain score | Post-treatment pain score ranges from 0 to 10 | Day 0, on the day of study intervention | |
Secondary | Change in voiding function in uroflowmetry | It is assessed by maximum flow rate in uroflowmetry | At baseline, 3 months, 6 months and 12 months after study intervention | |
Secondary | Change in urodynamic | Change in urodynamic function assessed by flowrate | At baseline, 3 months, 6 months and 12 months after study intervention | |
Secondary | Change in prostate size | Prostate size is assessed by transrectal ultrasound of prostate | At baseline, 3 months, 6 months and 12 months after study intervention |
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