Seal-G/ Seal-G MIST Long-Term Follow-up PMCF (Continue) Study

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-85
SponsorAdvanced Medical Solutions Ltd.

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

Treatment groups

208 Participants
are divided into 2 treatment groups

Locations

This trial has no locations