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Local antibiotic therapy in peri- implant inflammation

Sustained release of micro- spherical minocycline for management of peri-implant mucosal inflammation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013100114847N1
Enrollment
50
Registered
2014-01-25
Start date
2014-03-27
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Periimplantitis. Other complications of internal prosthetic devices, implants and grafts, not elsewhere classified

Interventions

Intervention 1: Control group: Mechanical debridement using ultrasonic scaler and air-powder air polishing device. Intervention 2: Intervention: Two weeks after mechanical debridement, a one mg of mi
Treatment - Devices
Treatment - Drugs
Control group: Mechanical debridement using ultrasonic scaler and air-powder air polishing device.
Intervention: Two weeks after mechanical debridement, a one mg of minocycline hydrochloride microspheres introduced subgingivally into the affected sites.

Sponsors

Vice Chancellor for research of Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1) Adults aged 18 or over with at least one implant in function for more than one year 2) Mild peri-imlant inflammatory diseases. defined as: presence of Bleeding on Probing, radio-graphic bon loss at the site of the implant less than 2 mm and probing depth more than 4 mm Exclusion criteria: 1) Any related systemic diseases 2) Smoking 3) Pregnancy and lactation 4) Active periodontal disease 5) Consumption of systemic antibiotics in the late 3 months 6) Need for bacterial prophylaxis with systemic antibiotics 7) Long-term use of any drug affects periodontal tissue conditions 8) Probing depth greater than 6 mm at base line visit 9) Drug and alcohol abuse 10) Uncontrolled diabetes 11) Probing depth less than 4 mm at base line visit

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bleeding on probing (BOP). Timepoint: Baseline, 2 week and 3 month later. Method of measurement: Periodontal Probe.

Secondary

MeasureTime frame
Peri implant probing depth. Timepoint: Baseline, after 2 weeks, after 3 month. Method of measurement: Periodontal prob.;Cytokines level in gingival crevicular fluid (GCF): IL-6, IL-17. Timepoint: Baseline, 2 week and 3 month later. Method of measurement: ELISA test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Pourabbas

Tabriz University of Medical Sciences

rpourabbas@tbzmed.ac.ir+98 41 1335 5965

Outcome results

None listed

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