A Post-market, Observational Registry With the easyEndoTM Universal Linear Cutting Stapler in Laparoscopic Bariatric Surgery (STAP-Delta)

  • End date
    May 31, 2025
  • participants needed
  • sponsor
Updated on 7 October 2022
bariatric surgery


The purpose of this observational registry is to evaluate the safety and performance of the easyEndoTM Universal Linear Cutting Stapler and reloads from Ezisurg Medical when used to create anastomoses during laparoscopic bariatric surgery. The goal of the study will be achieved by assessing the device performance and by reporting of peri- and postoperative complications in a prospectively maintained database.

Condition Obesity, Roux-en-Y Gastric Bypass, Gastrectomy, Mini Gastric Bypass
Treatment easyEndoTM Universal Linear Cutting Stapler and reloads (Ezisurg Medical)
Clinical Study IdentifierNCT04422236
Last Modified on7 October 2022


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Inclusion Criteria

Patient ≥ 18 years of age at registry entry
Patient and investigator signed and dated the informed consent form prior to the index-procedure
Patient has a BMI ≥ 35 kg/m2, with one or more related co-morbidities
Patient has a BMI ≥ 40 kg/m2
Patient is eligible for laparoscopic bariatric surgery

Exclusion Criteria

Patient is unable / unwilling to provide informed consent
Patient has a history of bariatric surgery
Patient is unable to comply with the registry protocol or proposed follow-up visits
Patient has a contra-indication for laparoscopic bariatric surgery
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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