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dc.rights.licenseopenen_US
dc.contributor.authorROBERT, G.
dc.contributor.authorDESCAZEAUD, A.
dc.contributor.authorKARSENTY, G.
dc.contributor.authorSAUSSINE, C.
dc.contributor.authorAZZOUZI, A. R.
dc.contributor.authorDE LA TAILLE, A.
dc.contributor.authorDESGRANDCHAMPS, F.
dc.contributor.authorFAIX, A.
dc.contributor.authorFOURMARIER, M.
dc.contributor.authorGEORGET, A.
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorBENARD, Antoine
dc.contributor.authorBARRY DELONGCHAMPS, N.
dc.date.accessioned2021-01-04T10:27:02Z
dc.date.available2021-01-04T10:27:02Z
dc.date.issued2018-06
dc.identifier.issn0724-4983en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/23608
dc.description.abstractEnOBJECTIVE: To explore efficacy and safety of Botulinum Neurotoxin Type A (BoNT-A) prostatic injection in patients with lower urinary tract symptoms (LUTS) due to benign prostatic hyperperplasia. MATERIALS AND METHODS: A phase 3 multicenter open-labeled study randomised patients to receive BoNT-A prostatic injection or optimized medical therapy. BoNT-A injection consisted in trans-rectal injections of 200 UI in the transitional zone of the prostate. Optimal medical therapy consisted in oral medication with any drug patented for LUTS. One month (M1) after randomisation patients in the BoNT-A group were asked to stop any medical therapy related to LUTS. The main judgment criterion was the IPSS score at M4. Per-protocol analysis was performed with a non-inferiority hypothesis (DeltaIPSS < 3). RESULTS: 127 patients were randomised to BoNT-A (n = 64) or medical therapy (n = 63). At randomisation mean IPSS was 16.9 +/- 7.2 in the BoNT-A group vs 15.7 +/- 7.3 in control. In the BoNT-A group, 44 patients (73.3%) could interrupt medical therapy for LUTS from M1 to M4. At M4, mean IPSS score was 12.0 +/- 6.7 in the BoNT-A group vs 11.8 +/- 6.9 in control. After adjustment for baseline IPSS, delta IPSS between groups was 0.01; 95% CI [- 2.14; 2.11] leading to accept the non-inferiority hypothesis. CONCLUSIONS: Four months after BoNT-A injection, most of the patients could interrupt LUTS-related medical treatments. In these patients, IPSS improvement was not inferior to optimized medical treatment, but the study design did not allow to conclude that this improvement was related with study drug rather than with sustained placebo effect. TRIAL REGISTRATION: NCT01275521.
dc.language.isoENen_US
dc.subject.enEMOS
dc.title.enProstatic injection of botulinum toxin is not inferior to optimized medical therapy in the management of lower urinary tract symptoms due to benign prostatic hyperplasia: results of a randomized clinical trial
dc.title.alternativeWorld J Urolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1007/s00345-018-2193-yen_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed29383480en_US
bordeaux.journalWorld Journal of Urologyen_US
bordeaux.page921-929en_US
bordeaux.volume36en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - U1219en_US
bordeaux.issue6en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.teamEMOSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03094145
hal.version1
hal.date.transferred2021-01-04T10:27:08Z
hal.exporttrue
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