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 volunteersQualifiers
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
Cohort
Prospective
Treatments tested in this trial
Liquid embolic agent
DeviceProstatic 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
Trial outcomes
Primary outcomes
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.
Secondary outcomes
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.
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.
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.
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.
Sponsors and contacts
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Assistance Publique - Hôpitaux de Paris
Lead sponsor
Balt International
Collaborator
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