Outcomes of Water Vapor Thermal Therapy (REZUM) in Management of Symptomatic Patients With Benign Prostatic Enlargement

Sponsor
Assiut University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05784909
Collaborator
(none)
50
1
13

Study Details

Study Description

Brief Summary

new treatment modality for BPH , less invasive and more effective.

Condition or Disease Intervention/Treatment Phase
  • Device: rezum
N/A

Detailed Description

Benign prostatic hyperplasia (BPH) is a common urological condition characterized by progressive increase in the size of the prostate gland. It is a disease of ageing, affecting 40% of men in their 50s and 90% of men over 90 years causing bladder outflow obstruction (BOO), which results in lower urinary tract symptoms (LUTS) which have a significant impact on quality of life (QoL).

The current management for LUTS caused by BOO secondary to BPH includes conservative approaches (watchful waiting and lifestyle modifications), pharmacotherapy and surgical intervention.

The Surgical interventions include open surgery (suprapubic and perineal approaches),transurethral resection of the prostate (TURP) which was a revolutionary step in the management of BPH, and was considered the first minimally invasive treatment for prostate enlargement and With the improvement of endoscopes, development and incorporation of new technologies into the medical field, minimally invasive procedures have been more and more introduced as surgical options to treat BPH .

Minimally invasive procedures include water vapor thermal therapy (REZUM), trans urethral needle ablation, trans urethral microwave thermotherapy, prostate urethral lift and prostate artery embolization.

REZUM (water vapor thermal therapy) is considered one of the advanced minimal invasive procedure that uses the principles of convective heat transfer that exploits the thermodynamic properties of water to remove the excess prostate tissue that is pressing on the urethra.

The therapy is targeted to a defined area because steam will travel only between cells until it encounters natural collagen barriers or the prostate capsule itself.

After the REZUM procedure, the body creates an inflammatory response, which takes two to four months to completely resolve. Initially, there will be swelling in the prostate, which can cause restriction of flow and cause more difficulty and frequency of urination.

In general, after the procedure symptoms will get worse before they get better and improved.

Erections are not affected by the REZUM procedure and there is 1% to 2% chance of retrograde ejaculation and his is a significantly lower percentage than in other prostate procedures.

Advantages of REZUM:
  • Can be performed under sedation only

  • Day case procedure

  • Strong short-term safety profile

  • No reports of de novo sexual dysfunction

  • Suitable for patients with an obstructing median lobe

  • Short procedure time

  • Good improvement in subjective and objective outcome measures: IPSS, QoL, Qmax and PVR

  • Cost effective

Disadvantages of REZUM:
  • Limited long-term data available

  • Not suitable for patients with history of recurrent urinary tract infections

  • Not suitable for large prostate size (>120 cc)

  • Not suitable for patients if prior invasive procedure for treatment of prostate or prior radiation on prostate

  • 50% patients require catheter post procedure

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Outcomes of Water Vapor Thermal Therapy (REZUM) in Management of Symptomatic Patients With Benign Prostatic Enlargement
Anticipated Study Start Date :
Apr 1, 2023
Anticipated Primary Completion Date :
Apr 1, 2024
Anticipated Study Completion Date :
May 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: patients diagnosed with bladder outlet obstruction due to BPH

all symptomatic patients with BPH with failure medical management or prefer minimal invasive procedure from the start.

Device: rezum
Technique With the patient in a lithotomy position, after cystoscopy, an RF current is applied to. Water vapour is delivered through a retractable vapor needle via emitter holes in the transurethral device. This is done in 9-second bursts to the transition zone of the prostate, where, via convection, it diffuses evenly throughout the target tissue. The depth of the needle penetrating is approximately 10 mm. Upon contact with body-temperature tissue, the water vapour then condenses. This phase shift to a liquid state dispenses concentrated energy onto the cell membranes of the target tissue, triggering instant cell necrosis. Overlapping injection sites can be established with repeated applications in order to fully target areas of hypertrophy. Saline flush irrigation is used to both cool the urethra and to promote visualization. At the end of the procedure Urethral catheter is fixed for 1-3 days.

Outcome Measures

Primary Outcome Measures

  1. evaluation of the IPSS [1 month after treatment]

    to assess the success of treatment ,pre-operative and postoperative questionnaire will be done

  2. duration of the operation [intra-operative]

    minutes or hours needed for the procedure

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • any patient diagnosed with BPH
Exclusion Criteria:
  • PATIENT REFUSING TO PARTICIPITATE

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Assiut University

Investigators

  • Study Director: Mohamed M Gadalmoulah, phd, professor

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Mohamed Ahmed Zamra, specialist of urology, Assiut University
ClinicalTrials.gov Identifier:
NCT05784909
Other Study ID Numbers:
  • REZUM in Assiut
First Posted:
Mar 27, 2023
Last Update Posted:
Mar 27, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 27, 2023