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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03104907
Other study ID # H-17000714-2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 22, 2017
Est. completion date November 27, 2018

Study information

Verified date November 2018
Source Rigshospitalet, Denmark
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to investigate the safety and efficacy of prostatic artery embolization of patients with recurrent symptoms secondary to locally advanced prostatic cancer including pelvic pain, bleeding or need for permanent urinary catheter who are unfit for or refuse surgical treatment.


Description:

This is a prospective study investigating the safety and efficacy of PAE for patients with prostate cancer who suffers from acute urinary retention, severe LUTS and/or recurrent complications such as haematuria.

Our hypothesis is that PAE will eliminate the need for indwelling catheter and improve IPSS and QoL 12 months post-procedure.

1, and 6 months follow-up.

Main outcome Ability to void after removal of indwelling catheter

Secondary outcomes International Prostate Symptom Score (IPSS) Quality of Life (QoL) International Index of Erectile Function (IIEF) Prostate volume Peak void flow (Qmax) Post-void residual (PVR) Classify complications according to Society of Interventional Radiology (SIR) guidelines for reporting Prostate-specific antigen (PSA)


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date November 27, 2018
Est. primary completion date November 27, 2018
Accepts healthy volunteers No
Gender Male
Age group N/A and older
Eligibility Inclusion Criteria:

- Indwelling catheter secondary to locally advanced prostate cancer (PCa) or

- Moderate-severe Obstructive LUTS secondary to PCa

- Unsuitable for or refuse surgery

Exclusion Criteria:

- Bladder dysfunction(and known neurological conditions affecting bladder function)

- Urethral strictures

- Bladder neck contracture

- Known sphincter anomalies

- Big bladder diverticulum or stones

- Kidney insufficiency (eGFR < 45)

- Coagulation disturbances

- Severe atheromatous or tortuosity of arteries

- Allergy to contrast medium

- Unable to undergo MR imaging

- Bladder malignancy

Study Design


Intervention

Procedure:
Prostatic Artery Embolization
The procedure is performed with the patient under local anaesthetic and if necessary sedation. We will be using a percutaneous transfemoral approach, super-selective catheterisation of small prostatic arteries is carried out using microcatheters. Embolisation will be done using microspherical embolic material.

Locations

Country Name City State
Denmark Rigshospitalet Copenhagen

Sponsors (1)

Lead Sponsor Collaborator
Rigshospitalet, Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ability to void spontaneously The ability to void after removal of the indwelling catheter 1 months
Secondary IPSS International Prostate Symptom Score 1, 6 months
Secondary QoL Quality of Life (scale) 1, 6 months
Secondary IIEF International Index of Erectile Function 1, 6 months
Secondary PV Prostate Volume 1, 6 months
Secondary PVR Post-void residual 1, 6 months
Secondary Qmax Peak void flow 1, 6 months
Secondary PSA Prostate-specific antigen 1, 24-hours, 6 months
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