Clinical Trial

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

Study acronym: NOQMOQS
Recruiting
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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.
Protocol Amendment History 1 change
notable Primary completion pushed: 2026-06 -> 2026-10 2026-08-14
Trial Details
NCT Number NCT05813236
Lead Sponsor Aesculap AG
Collaborators: B.Braun Surgical SA
Conditions Gingivitis, Gingival Diseases, Periodontal Diseases
Enrollment 84 participants
Start Date 2023-06-28
Primary Completion 2026-10 (estimated)
Study Completion 2026-12 (estimated)
Updated on ClinicalTrials.gov 2026-08-13