Titanium mesh efficacy in peri-implantitis

Treatment of extensive peri-implant defects with titanium mesh

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190712044177N1

Enrollment

Registered

2021-04-25

Start date

2021-01-10

Completion date

Unknown

Last updated

2021-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Peri-implantitis. Post-osseointegration biological failure of dental implant

Interventions

Intervention group: The patients had at least one titanium implant with peri-implantitis with a pocket probing depth (PD) = 6 mm, positive bleeding and/or pus on probing, and peri-implant bone loss >

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with peri-implantitis (bone loss, increased probing depth compared to previous visits and BoP and/or pus; in the absence of previous data, defects with = 3 mm depth, probing depth = 6 mm, and bleeding on probing and/or pus) At least 30-50% Peri-implant bon loss

Exclusion criteria

Exclusion criteria: Smoking O'Leary plaque index > 20% Allergy to the material used in the study Pregnancy Uncontrolled peri-implantitis Parafunctional habits Systemic disease or intake of any medication

Design outcomes

Primary

Measure	Time frame
Radiographic defect fill. Timepoint: Eight months following surgery. Method of measurement: Measurement using a digital software considering the implant dimension for calibration.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahdi Kadkhodazadeh

Shahid Beheshti University of Medical Sciences

mahdi.sbmu@gmail.com+98 21 2240 3075

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026