Phase
Condition
Hemorrhage
Prostate Cancer, Early, Recurrent
Prostate Disorders
Treatment
Arm A - Application of 5g of ARISTA™ AH
Clinical Study ID
Ages 45-68 Male
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age range ≥ 45 to ≥68 yrs
Biopsy proven prostate cancer treated with robotic-assisted radical prostatectomy
Intrafascial nerve sparing surgery (unilaterally or bilaterally)
Preoperative urinary continence
Group A Preoperative unassisted International Index of Erectile function (IIEF)-5score range 8-16 (i.e. moderate (8-11) and mild to moderate (12-16))
Exclusion
Exclusion Criteria:
Severe intellectual limitations preventing to fully understand the study concept andits content
High risk prostate cancer (PSA ≥ 20 ng/ml or biopsy Gleason-Score ≥ 8 or suspectedT4)
Suspected bone or visceral metastases at preoperative imaging Neoadjuvant androgendeprivation therapy
Any prior local therapy of the prostate (including subvesical deobstruction orradiation therapy)
Any prior chemotherapy or colon/rectal surgery
Any prior pelvic trauma that required surgical intervention
Depression or other psychological or neurological disease (dementia, schizophrenia,bipolar disorder etc.)
Peyronie's disease
Polyneuropathia
IPSS Score >19 and QoL >3
Bilateral secondary (complete or partial) resection of the neurovascular bundle
No contraindications for phosphodiesterase type 5 inhibitor intake (i.e. suited formost penile rehabilitation regimes)
Any endocrine function disorder (not including diabetes)
SURGICAL AND PERIOPERATIVE EXLUSION CRITERIA:
Accessory pudendal arteries (APA) preservation, if an APA is identified
For a) nerve sparing and b) controlling bleeding in the area of the prostate bed andneurovascular bundles after prostate removal, no monopolar thermal application areallowed but suturing and clip application is allowed. For secondary resection of theneurovascular bundle and controlling bleeding, mono- or bipolar thermal application,clip application and suturing is allowed.
No surgical revision within 7d after RARP (Clavien Dindo classified complication ≥3b)
No definitive anastomotic partial or complete rupture (identified via cystogramwithin 30d after RARP)
Study Design
Connect with a study center
Martini Klinik am UKE GmbH
Hamburg, HH 20246
GermanySite Not Available
St. Antonius-Hospital Gronau GmbH, Klinik für Urologie, Urologische Onkologie und Roboter-assistierte Chirurgie
Gronau, NRW 48599
GermanyActive - Recruiting
Klinik und Poliklinik für Urologie des Universitätsklinikums Leipzig
Leipzig, Saxony 04103
GermanySite Not Available
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