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dc.creatorPerivoliotis K., Spyridakis M., Zintzaras E., Arnaoutoglou E., Pramateftakis M.-G., Tepetes K.en
dc.date.accessioned2023-01-31T09:47:30Z
dc.date.available2023-01-31T09:47:30Z
dc.date.issued2021
dc.identifier10.1007/s00384-020-03768-8
dc.identifier.issn01791958
dc.identifier.urihttp://hdl.handle.net/11615/78074
dc.description.abstractBackground: In this study, we proposed a combined outpatient treatment modality for hemorrhoidal disease. Methods: This study was a prospective non-inferiority randomized controlled trial (RCT). The experimental group included the dearterialization and hemorrhoidopexy under pudendal nerve block, whereas the comparator consisted of the standard Doppler guided hemorrhoidal artery ligation and hemorrhoidopexy, under spinal anesthesia. As primary hypothesis, we considered the non-inferiority of the proposed modality in terms of the presenting symptom remission rate (non-inferiority margin: 10%). Randomization was based on a 1:1 ratio. Blinding was confined to the patient and the investigator. Results: Overall, 60 patients were enrolled. The primary hypothesis of this RCT (96.7% vs 73.3%) was validated. The experimental group was associated with a lower operation duration and an expedited onset of mobilization and feeding. Moreover, a favorable profile regarding short-term morbidity and analgesia was identified. The control group displayed a higher pile recurrence rate and a suboptimal patient satisfaction. A significant effect of the treatment modality in most of the SF-36 components was confirmed. Conclusions: The proposed treatment modality was associated with favorable short and long-term outcomes. Due to specific limitations, further RCTs, with a larger sample size, are required. Trial Registration ClinicalTrials.gov: NCT03298997. © 2020, Springer-Verlag GmbH Germany, part of Springer Nature.en
dc.language.isoenen
dc.sourceInternational Journal of Colorectal Diseaseen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85092115901&doi=10.1007%2fs00384-020-03768-8&partnerID=40&md5=de9533163a889985afc07ce5a7652b09
dc.subjectadulten
dc.subjectArticleen
dc.subjectclinical articleen
dc.subjectclinical effectivenessen
dc.subjectcomparative effectivenessen
dc.subjectcontrolled studyen
dc.subjectDoppler ultrasonographyen
dc.subjectfemaleen
dc.subjectfood intakeen
dc.subjectgastrointestinal surgeryen
dc.subjecthemorrhoiden
dc.subjecthemorrhoidal artery ligationen
dc.subjecthemorrhoidectomyen
dc.subjecthumanen
dc.subjectmaleen
dc.subjectmiddle ageden
dc.subjectmobilizationen
dc.subjectmorbidityen
dc.subjectnerve blocken
dc.subjectoperation durationen
dc.subjectoutcome assessmenten
dc.subjectoutpatient careen
dc.subjectpatient satisfactionen
dc.subjectpriority journalen
dc.subjectprospective studyen
dc.subjectpudendal nerveen
dc.subjectrandomized controlled trialen
dc.subjectrecurrent diseaseen
dc.subjectremissionen
dc.subjectShort Form 36en
dc.subjectspinal anesthesiaen
dc.subjectvalidation processen
dc.subjectadverse eventen
dc.subjectarteryen
dc.subjectligationen
dc.subjecttreatment outcomeen
dc.subjectArteriesen
dc.subjectHemorrhoidectomyen
dc.subjectHemorrhoidsen
dc.subjectHumansen
dc.subjectLigationen
dc.subjectPudendal Nerveen
dc.subjectTreatment Outcomeen
dc.subjectSpringer Science and Business Media Deutschland GmbHen
dc.titleNon-Doppler hemorrhoidal artery ligation and hemorrhoidopexy combined with pudendal nerve block for the treatment of hemorrhoidal disease: a non-inferiority randomized controlled trialen
dc.typejournalArticleen


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