Efficacy of Prostatic Arteries Embolization Using SQUIDPERI

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age18+
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

Prostatic Artery Embolization (PAE) is a recognized mini-invasive treatment of bothersome Lower Urinary Tract Symptoms (LUTS) related to Benign Prostatic Hyperplasia (BPH). Particle embolics are used almost exclusively for embolization, with wide variation in the type and size of particles showing similar performance and safety results. Even if its durability relies on multiple risk factors, LUTS recurrence-free survival probability decreases with years. It is demonstrated that recanalization of the native prostatic artery is found in 66% of patients experiencing LUTS recurrence. Artery recanalization after several months has been reported in embolization with microparticles. The investigators addressed this issue using the liquid embolic agent SQUIDPERI in a prospective cohort of patients undergoing rePAE and showed a good clinical success rate (76.7%) at 3 months. Since then, the investigators perform initial PAE using SQUIDPERI with good results.

The aim of SQUID-PAE study is to assess the efficacy of PAE using SQUIDPERI in an initial PAE setting in a multicenter prospective study.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥18 years

Patient scheduled for a PAE using SquidPERI as part of routine care

Patient informed who signed the informed consent form

French social security affiliation

Disqualifiers

Patient unwilling or unlikely to comply with FU schedule

Known severe allergy to iodine

Known severe hepatic impairment

Vulnerable patient populations (such as patient under guardianship, curatorship, deprived of liberty)

Trial population

Nonvulnerable men suffering from LUTS related to BPH and eligible to PAE.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Liquid embolic agent

    Device

    Prostatic Artery Embolization using a non-adhesive liquid embolic agent composed of an EVOH (ethylene-vinyl alcohol) copolymer dissolved in DMSO (dimethyl sulfoxide), with micronized tantalum powder suspended within it

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: Study group1 intervention

Trial outcomes

Primary outcomes

1

Clinical success at 3 months

Rate of clinical success defined as an IPSS \<18 at follow-up with a decrease from baseline \> 25% AND a quality of life (QoL, last question of IPSS questionnaire) \< 4 at follow-up with a decrease from baseline ≥ 1.

Time frame
Baseline and 3 months

Secondary outcomes

1

Immediate technical success

Rate of immediate technical success. Immediate technical success is defined as an embolization of both lobes of the prostate using SQUID PERI.

Time frame
Embolization procedure (baseline)
2

Clinical success at 6 months

Rate of clinical success defined as an IPSS \<18 at follow-up with a decrease from baseline \> 25% AND a quality of life (QoL, last question of IPSS questionnaire) \< 4 at follow-up with a decrease from baseline ≥ 1.

Time frame
Baseline and 6 months
3

Clinical success at 9 months

Rate of clinical success defined as an IPSS \<18 at follow-up with a decrease from baseline \> 25% AND a quality of life (QoL, last question of IPSS questionnaire) \< 4 at follow-up with a decrease from baseline ≥ 1.

Time frame
Baseline and 9 months
4

Clinical success at 12 months

Rate of clinical success defined as an IPSS \<18 at follow-up with a decrease from baseline \> 25% AND a quality of life (QoL, last question of IPSS questionnaire) \< 4 at follow-up with a decrease from baseline ≥ 1.

Time frame
Baseline and 12 months

Other outcomes

Sponsors and contacts

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