Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05813236

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

Led by Aesculap AG · Updated on 2026-03-06

84

Participants Needed

1

Research Sites

178 weeks

Total Duration

On this page

Sponsors

A

Aesculap AG

Lead Sponsor

B

B.Braun Surgical SA

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patient undergoing resective periodontal surgery with one of the following incisions: crestal, vertical, intrasulcular, or submarginal
  • Written informed consent for data collection in the randomized controlled trial
Not Eligible

You will not qualify if you...

  • Emergency surgery
  • Pregnancy
  • Breastfeeding
  • Taking medication that might affect wound healing
  • Having a condition that might affect wound healing
  • Allergy or hypersensitivity to the suture material

AI-Screening

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Trial Site Locations

Total: 1 location

1

Facultat d'Odontologia. Universitat Internacional de Catalunya

Sant Cugat del Vallès, Catalonia, Spain, 08195

Actively Recruiting

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Research Team

J

Jaume García López, Dr.

CONTACT

J

Jose Manuel Molina, Dr.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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