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NCT Number: NCT04084938

Artery Embolization vs Operation of Benign Prostate Hyperplasia

Aim of the study is to compare prostate artery embolization (PAE) to the established surgical treatment for patient acceptance, morbidity, complications, and the functional outcomes. To compare length of stay, hospital costs and time for recovery. 140 patients will be randomized to PAE or surgery. Patients should suffer from lower urinary tract symptoms (LUTS), be candidates for both treatments and willing to undergo both procedures. Before randomization computed tomography angiography of the pelvic arteries is done to select eligible patients. Magnetic resonance imaging of prostate rules out possible cancer. The PAE is done in the angio suite in the radiology department injecting small particles into the prostate arteries. The surgery is done in the operation room in the urology department according to established procedures. Clinical follow-up include clinical visit after 3 months, 1 and 5 years. Acute as well as long term complications will be recorded.

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Key information

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Oslo University Hospital, Aker

Oslo, Norway

Location status: Recruiting

Location contact

Dag Bay, MD

SUB_INVESTIGATOR

Eduard Baco, MD, PHD

CONTACT

[email protected]

+4795221378

Erik Rud, MD, PHD

SUB_INVESTIGATOR

Gunnar Sandbæk, MD, PHD

SUB_INVESTIGATOR

Nils Einar Kløw, MD, PHD

PRINCIPAL_INVESTIGATOR

Ole Jørgen Grøtta, MD, PHD

SUB_INVESTIGATOR

Rolf Eigil Berg, MD, PHD

SUB_INVESTIGATOR

Thijs Hagen, MD

CONTACT

[email protected]

+4745002349

Truls E Bjerklund Johansen, MD, PHD

SUB_INVESTIGATOR

About this study

Background: Prostatic artery embolization (PAE) has recently been described as a promising alternative to surgery for treatment of lower urinary tract symptoms (LUTS) due to an enlarged, benign prostate. The treatment has not been implemented into international guidelines and has only been introduced to few patients in Norway.

Purpose: To compare PAE to the established surgical treatment for patient acceptance, morbidity, complications, and the functional outcomes. To compare length of stay, hospital costs and time for recovery.

Materials and Methods: 140 patients will be randomized to PAE or surgery. Patients should suffer from LUTS, be candidates for both treatments and willing to undergo both procedures. Before randomization computed tomography angiography of the pelvic arteries is done to select eligible patients. Magnetic resonance imaging of prostate rules out possible cancer. The PAE is done in the angio suite in the radiology department injection small particles into the prostate arteries. The surgery is done in the operation room in the urology department according to established procedures. All patients stay in the urology unit after the procedure. Clinical follow-up include clinical visit after 3 months, 1 and 5 years. Acute as well as long term complications will be recorded. The patients fill in the form of quality of life from urologic disease. Urodynamic examination will record functional outcome. Length of stay, procedure costs and recovery time will be recorded.

Importance of the study: Contribute to establishment of new treatment and help to select the right patients for the alternative treatments. Randomized study will give important information to the international community. It is possible to run this study in Norway because it is still in limited use.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • LUTS from Benign Prostate Hyperplasia (BPH) with moderate and severe IPSS score (IPSS > 8) and QoL = or >3
  • and refractory to medical treatment for at least 6 months or the patient is unwilling to accept medical treatment
  • or BPH using permanent or intermittent catheterization
  • Prostate volume > 50 ml
  • Signed informed consent

Exclusion criteria

  • Urological disorders: evidence of clinically significant prostate cancer [as defined by START criteria] on prostate biopsy (27,28), prostatitis (29,30), detrusor-sphincter dyssynergia or evidence of neurogenic bladder, urethral strictures, bladder neck contracture, bladder stone or bladder cancer
  • Renal insufficiency defined as Glomerular Filtration Rate < 30 ml/min/1,73m2
  • Known severe reactions to iodine-based contrast or gadolinium-based contrast
  • Previous prostate operation
  • CT examination reveals no access to the prostate arteries.

Treatment and study plan

Prostate operation or prostate artery embolization

Procedure

As described above.

Primary outcomes

  1. Quality of life due to urinary symptoms

    Time frame: 3 months

    "Quality of life due to urinary symptoms" QoL = or <3 The scale used: Quality of Life Due to Urinary Symptoms. Scale from 0 to 6, the worse is 6. The patient question: If you were to spend the rest of Your life With Your urinary condition just the way it is now, how would you feel about that?

  2. Number of patients with Prostate Artery Embolization that did not have prostate operation

    Time frame: 12 months

    The investigators will record the number of patients that did not have prostate surgery after Prostate Artery Embolization. After 3 months the patients will be offered operation when Quality of Life Due to Urinary Symptoms is 4-6 on the scale from 0-6 ie. the patients report unsatisfied (4), unhappy (5) or terrible (6).

Secondary outcomes

  1. Number of patients with postoperative complications

    Time frame: 3 months

    Postoperative complications will be recorded according to the Clavien-Dindo classification system. Complication will be recorded during hospital stay, at the follow-up after 3 months and at any intermediate points reported by the patients

  2. Hospital stay

    Time frame: 3 months

    Length of stay including before and after the intervention

  3. Symptoms

    Time frame: 3 months, 1 year, 5 years

    Change in IPSS. The patients fill in the form International Prostate Symptom Score (IPSS) before and after treatment. Seven questions are scored from 0 to 5, 5 is the worst outcome. Total score from 0 - 35. 1-7 is mild symptoms, 8-19 is moderate symptoms, 20-35 is severe symptoms.

Other outcomes

  1. Need for catheters

    Time frame: 3 and 12 months

    Number of patients using permanent and intermittent catheters at follow-up will be recorded

  2. Erectile function

    Time frame: 3 and 12 months

    Change in erectile function will be recoded using the International Index of Erectile Function (IIEF-5) questionnaire. The patients fill in the form before and after treatment. There are 5 questions which score 1-5, 5 is the best. Total score from 5-25.

  3. Ejaculation

    Time frame: 3 and 12 months

    Change in ejaculation will be recorded using the Male Sexual Questionnaire short form for assessing ejaculation. There are 4 questions with 5-6 possible outcomes.

Study contacts

Contact information is provided by the study sponsor or research team.

Eduard Baco, MD, PHD

CONTACT

[email protected]

+47 95221378

Thijs Hagen, MD

CONTACT

[email protected]

+ 47 45002349

Sponsors and collaborators

Lead sponsor

Oslo University Hospital

Other

Registry information

Official study title

Prostatic Artery Embolization vs Transurethral Resection of the Prostate or Open Prostatectomy in Patients With Symptomatic Benign Prostatic Hyperplasia

Acronym: NORTAPE

Important dates

Study start
2019
Primary completion
2024
Study completion
2027
First posted
Sep 10, 2019
Registry last updated
Dec 27, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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