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Study identifier: NCT05782010 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

SCI-Pex Study - Safety and Performance of PexyEazy®, a Device for Treatment of Hemorrhoids

Condition: Hemorrhoids · Hemorrhoids, Internal · Suture; Complications, Infection or Inflammation  ·  Sponsor: Developeration AB

PhaseNA
Planned participants35
Who can joinAll sexes, 18 Years to 84 Years
Healthy volunteersNo

About this study

The SCI-Pex study is a multicenter, prospective, non-controlled investigation on PexyEazy®, a new device for treatment of hemorrhoids based on the mucopexy method. Mucopexy is a well established method where sutures are applied above the hemorrhoids. When knots are tied, the hemorrhoids are lifted inwards to their normal position, which makes them swell down and symptoms disappears. PexyEazy® perform a mukopexy in a semiautomatic, faster and easier way on awake patient in less than 10 minutes. The SCI-Pex study will evaluate the safety and performance of PexyEazy on 35 patients with hemorrhoids grade II and III with a follow-up after 1 week, 3 months and 1 years. Adverse events, pain and other complications will be recorded, quality of life and hemorrhoid symptom questionnaires and clinical examination after 3 months and 1 year will be monitored to evaluate the result after a PexyEazy® procedure.

This description comes directly from the study's public registry record.

Talk to the study team

Johan Ungerstedt, Dr  ·  +46709427842  ·  johan.ungerstedt@developeration.se

Ulf Kressner, Dr  ·  ulfkressner@icloud.com

Always discuss trial participation with your own doctor first.

Locations (3)

Frölunda SpecialistsjukhusFrölunda, SwedenRecruiting
Norrtälje SjukhusNorrtälje, SwedenRecruiting
Capio kirurgkliniken, SophiahemmetStockholm, SwedenNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT05782010