ClinicalTrials.Veeva

Menu

Clinical and Radiological Evaluation of Two Mastoid Filling Products (MASTOS)

R

Regional University Hospital Center (CHRU)

Status

Unknown

Conditions

Prospective Study

Study type

Observational

Funder types

Other

Identifiers

NCT05072678
29BRC21.0018 (MASTOS)

Details and patient eligibility

About

to compare, the osseous density in the mastoid of two products used to obliterate the mastoid during surgery for cholesteatoma

Full description

Primary objective: To compare the radiological aspect in the petrous bone of two obliteration products in adults, one year after surgery (Bioactive Glass S53P4 and biological Hydroxy apatite) secondary objective : To evaluate the cutaneous and the inner ear tolerance of bioactive glass S53P4 and biological hydroxy apatite when used in the mastoid and epitympanic obliteration for chronic otitis surgery

Enrollment

20 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult with cholesteatoma surgery Accepting the protocol and the radiological follow-up

Exclusion criteria

  • patient less than 18 years old

Trial contacts and locations

1

Loading...

Central trial contact

sonia Sahli Vivi Corsi, MD; remi Marianowski, MD, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems