Registry record of a completed single-arm feasibility study in a small population (n=25) evaluating a novel device; no results are posted, and the primary focus is procedural feasibility and safety rather than clinical efficacy.
Reported
Planned sample size25
Primary outcome – feasibility and…Side-to-side anastomosis for duodeno-ileal…
Primary outcome – safety assessme…Day 90, Day 180, Day 360