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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAesculap AG

About this trial

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.

Eligibility criteria

Qualifiers

Crestal incision

Vertical incision

Intrasulcular incision

Submarginal incision

Disqualifiers

Emergency surgery.

Pregnancy.

Breastfeeding

Patients taking medication that might affect wound healing.

Trial design

Treatments tested in this trial

  • Novosyn® in resective periodontal surgery
  • Monosyn® in resective periodontal surgery

Treatment groups

84 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Aesculap AG

Lead sponsor

B.Braun Surgical SA

Collaborator