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

A

Assiut University

Status

Not yet enrolling

Conditions

Benign Prostatic Hyperplasia

Treatments

Device: rezum

Study type

Interventional

Funder types

Other

Identifiers

NCT05784909
REZUM in Assiut

Details and patient eligibility

About

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

Full 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

Enrollment

50 estimated patients

Sex

Male

Ages

50+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • any patient diagnosed with BPH

Exclusion criteria

  • PATIENT REFUSING TO PARTICIPITATE

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

patients diagnosed with bladder outlet obstruction due to BPH
Experimental group
Description:
all symptomatic patients with BPH with failure medical management or prefer minimal invasive procedure from the start.
Treatment:
Device: rezum

Trial contacts and locations

0

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Central trial contact

Mohamed A Zamra, Msc

Data sourced from clinicaltrials.gov

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