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NOVOSYN® Quick Versus MONOSYN® Quick Suture Material in Resective Periodontal Surgery — NOQMOQS  

Periodontal Diseases Clinical Trial

Official title:
Randomized, Monocentric, Double Blinded, Prospective Study to Evaluate the Early Wound Healing After the Utilization of NOVOSYN® Quick Versus MONOSYN® Quick Suture Material in Resective Periodontal Surgery

Clinical Trial Summary

The aim of this study is to prove that Novosyn Quick and Monosyn Quick are equivalent in early wound healing in adult patients undergoing resective periodontal surgery. In order to show equivalence between Novosyn Quick and Monosyn Quick EHS, which is composed of 3 parameters: clinical signs of reepithelization, clinical signs of haemostasis and clinical signs of inflammation, will be calculated for each suture 10 ± 5 days postoperatively and cannot differ more than 2 points. Furthermore, complications, the handling of the suture material, pain, satisfaction of the patient and bacterial contamination of the thread (optional) will also be assessed as secondary objectives.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05813236
Study type Interventional
Source Aesculap AG
Contact Aina Fernández Rodríguez
Phone +34935866200
Email info@bbraun.com
Status Recruiting
Phase N/A
Start date June 28, 2023
Completion date July 2025
View Details
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