Skip to main content
OpenTrials
Completed

NCT Number: NCT06160388

The Safety of S53P4 Bioactive Glass for Mastoid Obliteration

In recent years, mastoid obliteration (MO) after mastoidectomy has gained popularity. However, the choice for obliteration material has been a point of discussion. Autologous materials have the advantage of being freely available without cost.Synthetic materials on the other hand have unlimited supply, hold volume over time and have no risk of donor site morbidity. Comparative studies between materials are rare and the few available were unable to ascertain superiority.

Our hospital has been utilizing the same material for obliteration since 2011: S53P4 bioactive glass (BAG). It since has become our main operating procedure to obliterate the mastoid cavity with BAG granules following both canal wall up (CWU) and canal wall down (CWD) mastoidectomy. This bioactive glass has several important characteristics, such as the retaining of volume over time and antibacterial properties.

An important factor when selecting obliteration material is safety. Data on this was reported in several studies, but unfortunately these studies only investigated short-term safety in small and selected cohorts of patients, often without comparison. Additionally, large studies with extensive follow-up are necessary to detect rare complications and long-term pitfalls. Therefore, the aim of this study is to determine the safety of BAG in a cohort that encompasses all cases that underwent CWU+MO and CWD+MO in our institute and compare these results to a non-obliteration cohort. The main outcomes are short- and long-term safety, as indicated by surgical complications in the first year following surgery and revision surgeries during follow-up, respectively. The investigators will compare the obliteration cohort to the non-obliteration cohort, hypothesizing that obliteration results in a comparable or lower rate of complications and revision surgeries

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Sex eligibility

All sexes

Study type

Observational

Primary location

Diakonessenhuis

Utrecht, 3582KE, Netherlands

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Canal wall up or canal wall down mastoidectomy
  • Operated between 2010 and 2022
  • All indications are included

Exclusion criteria

  • Other surgical techniques, such as subtotal petrosectomy

Treatment and study plan

S53P4 Bioactive glass

Device

Following mastoidectomy, the mastoid cavity, and if the ossicular chain has been removed the epitympanum as well, are obliterated using S53P4 bioactive glass. The bioactive glass is mixed with saline and administered to the cavity, ensuring a tight fit.

Primary outcomes

  1. The number of patients with postoperative surgical complications in the first year following surgery

    Time frame: First year following surgery

    Complications that occured within the first year following surgery

    We compare the obliteration cohort to the non-obliterative cohort

  2. The number of patients which require revision surgery during follow-up

    Time frame: At 3-, 5- and 8-years postoperatively

    Revision surgeries performed during follow-up due to problems with the obliteration

Sponsors and collaborators

Lead sponsor

Diakonessenhuis, Utrecht

Other

Registry information

Official study title

The Short- and Long-Term Safety of S53P4 Bioactive Glass for Mastoid Obliteration: a Retrospective Comparative Study

Important dates

Study start
2023
Primary completion
2024
Study completion
2025
First posted
Dec 7, 2023
Registry last updated
Jul 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.