Prostate Embolization for Acute Urinary Retention Study (PARIS1)

Clinsearch GmbH

Status

Unknown

Conditions

Prostatic Hypertrophy, Benign

Treatments

Device: Bead Block

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT02689830

SA-112043

Details and patient eligibility

About

The purpose of this study is to assess the feasibility and safety of Prostate Artery Embolization (PAE) in patients suffering of Acute Urinary Retention (AUR) in the context Benign Prostatic Hypertrophy (BPH).

Full description

This is an open-label prospective, multicenter (centralized procedure), single arm, sequentially enrolling study. Twenty subjects will be enrolled in the study.

Patient will be referred by the attending urologists after failure of the currently recommended approach of Trial WithOut Catheter (TWOC) and alpha-adrenergic receptor (AR) blockers.

It is expected that all AUR cases referred to the local urological clinic will be considered for inclusion in the trial. A trial log book will be completed by the referring local urologist in order to obtain preliminary data on the applicability of the trial to all AUR comers in the institution. This log book will be limited to a very simple questionnaire to ensure high rate of completion by the attending resident/fellow (Patients age, size of prostate, previous Benign Prostate Hypertrophy symptoms, renal function). It will be used in order to assess the external validity of this first phase trial and will be a help to design the potential next step trial.

When a patient will present with AUR in the corresponding urological clinic, the PI and Clinical research coordinator will be informed by a short text message, fax or e-mail in order to prepare the following process.

Patient will be informed by the urologist of the ongoing research project. In summary, this will consist in informing the patient that the first step is TWOC and in case of failure of TWOC several options are offered including PAE in the trial setting. Inclusion of the patient will considered only in case of failure of TWOC.

If the patient is willing to participate, patient will be seen in clinic by the Principal Investigator or co-investigator in order to inform him of the protocol and obtain signed informed consent.

PAE will be scheduled upon the first contact to make sure that PAE is performed in a short delay following failure of TWOC. The goal is to perform PAE in the week following recatheterization. For practical reasons this delay might be extended and will be recorded in the Case Report Form.

Enrollment

20 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

AUR Patients presenting with a first episode of AUR related to BPH (no matter if previously known or not) AND
Failure of at least one TWOC AND
Prostate size > or = 50 ml (ultrasound measurement)

Exclusion criteria

Known hypocontractile bladder
AUR related to other causes (Acute prostatitis or documented Prostate cancer)
Severe iodine allergy
Known prostate cancer
Known ongoing acute or chronic prostatitis
On-going acute pyelonephritis or septicemia from urinary origin
Patient refusing PAE
Severe renal failure (creatinine Clearance < 20 ml/min (MDRD)
Contra-indication to AR blockers (postural hypotension micturition syncope)
Contra-indication to anticoagulants
Patient catheterized with a suspubian catheter
Patient <18
Patients who are prisoners
Patients who are mentally incapacitated
Patients participating in an investigational study involving the peripheral vasculature
Patients unable or unwilling to provide written informed consent
Patients ineligible for pelvic angiography and embolization including severe atheromatous condition or any anatomical condition