Randomized Controlled Trial, Human Study Clinical Trial
Official title:
Propylene Mesh VS Standard Customized Palatal Stent as Protective Mechanical Barrier Following Harvesting of a Free Palatal Graft: A Short-term Pragmatic Randomized Clinical Trial (Part 1)
protection of the palatal wound is an essential step following harvesting a palatal soft tissue graft. During the last decades, several materials were used to avoid protect against the post-operative problems as bleeding, pain and possible infections. The aim of this randomized clinical trial was to assess the usage of polypropylene mesh, compared to the conventional custom-made acrylic stent for efficacy in protection of the palatal wound and reducing the bleeding tendency and post-operative pain. propylene mesh is a promising material for protection of the palatal wound due to its light weight, limited bacterial wicking, tissue compatible properties, however, the custom made acrylic palatal stent provides a more precise mechanical . More studies are required to deeply assess the benefits of this material in the periodontal plastic surgeries.
Background: protection of the palatal wound is an essential step following harvesting a
palatal soft tissue graft. During the last decades, several materials were used to avoid
protect against the post-operative problems as bleeding, pain and possible infections. The
aim of this randomized clinical trial was to assess the usage of polypropylene mesh, compared
to the conventional custom-made acrylic stent for efficacy in protection of the palatal wound
and reducing the bleeding tendency and post-operative pain.
Patients and methods: A single blinded, parallel group randomized controlled trial took
place. Twenty sites were approved to be treated using soft tissue grafting technique with the
need for a palatally harvested free graft. The palatal wounds were protected with propylene
mesh and custom-made acrylic palatal sten. Participants were qualitatively assessed for
bleeding duration, bleeding amount, pain duration, infection possibility, inflammation at 2,
4, 6, 8, 14 days post-operatively. The patient acceptance was also evaluated.
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