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

Study acronym: NOQMOQS
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 3 months later Jun 2026 → Oct 2026
See other at-risk trials from Aesculap AG

Record History

  1. Primary completion pushed from Jun 2026 to Oct 2026v7
  2. Primary completion date: Jan 2026 to Jun 2026 Completion date: Jul 2026 to Dec 2026v6 Show 1 more changeShow less
    • Completion date: Jul 2026 to Dec 2026
  3. Primary completion date: Jan 2025 to Jan 2026 Completion date: Jul 2025 to Jul 2026v5 Show 1 more changeShow less
    • Completion date: Jul 2025 to Jul 2026
  4. Primary completion date: Jan 2024 to Jan 2025 Completion date: Jul 2024 to Jul 2025v4 Show 1 more changeShow less
    • Completion date: Jul 2024 to Jul 2025
  5. Trial status: Not Yet Recruiting to Recruiting Start date changed from estimate of Jun 2023 to Jun 28, 2023 · Site details revisedv3 Show 2 more changesShow less
    • Start date changed from estimate of Jun 2023 to Jun 28, 2023
    • Site details revised
  6. Interventions: resective periodontal surgery (Device) to Monosyn® in resective periodontal surgery (Device), Novosyn® in resective periodontal surgery (Device) Secondary endpoints revised (12)v2 Show 1 more changeShow less
    • Secondary endpoints revised (12)

    See this version in full on ClinicalTrials.gov ↗

  7. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Aesculap AG
32 trials monitored
See 6 trials at risk
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.
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
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov