About this trial
Postoperative complications following colon anastomosis surgery, such as adhesions, stenosis, stricture and obstruction, can significantly impact patient outcomes. The use of surgical sealants has been proposed as a means to mitigate anastomotic complications by providing a protective barrier over the anastomosis site, reducing the risk or the severity of anastomotic leak. The previous post-market clinical follow-up (PMCF) study assessed the short-term safety and performance of SEAL-G surgical sealants in preventing anastomotic leaks and early post-operative complications. However, long-term data are needed to establish its sustained safety and effectiveness.
This continuation study aims to evaluate the long-term impact of the SEAL-G/MIST surgical sealant on post-operative complications over 12+ months after surgery. The study will compare complication rates in patients treated with the surgical sealant to a retrospective comparable control group who underwent similar procedures without the sealant.
Eligibility criteria
Qualifiers
Treatment Group: Patients participated and completed all visits in the previous PMCF study (treatment group; #DLG-072-06)
Control Group: comparable retrospective subjects that meet the same inclusion criteria specified in #DLG-072-06.
Disqualifiers
Patients with missing or incomplete medical records that prevent retrospective comparison.
Patients that during the original surgery received any treatment on the anastomosis (sealant/glue) except for the anastomosis closure technique (sutures/staple).
Original surgery included stoma creation.
Trial design
Treatments tested in this trial
- long-term follow up visit