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The comparison of the effect of tetracycline sterile ophthalmic ointment as an adjvant in peri-implantitis treatment

The comparison of the effect of tetracycline sterile ophthalmic ointment as an adjvant to mechanical debridement and mechanical debridement alone in peri-implantitis treatment

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210909052418N1
Enrollment
32
Registered
2021-10-31
Start date
2021-11-06
Completion date
Unknown
Last updated
2021-11-01

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

Conditions

peri-implantitis. Other endosseous dental implant failure

Interventions

Intervention 1: Intervention group: After local anesthesia (Xylocaine Dental (lidocaine HCl)) and isolation and drying of tetracycline ointment (AEROTEX) surfaces by placing a flexible needle (cannula

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: Presence of pre-implant disease No history of pre-implant surgery treatment PD>6 mm Positive BOP BOL<2mm No use of antibiotics and mouthwash and periodontal treatment in the last 6 weeks. No use of antibiotics and mouthwash and periodontal treatment in the last 6 weeks

Exclusion criteria

Exclusion criteria: Pregnancy and breast feeding Using anticoagulants Allergy to tetracycline sterile eye ointment Underlying disease (diabetes, kidney disorders, etc.) Smoking

Design outcomes

Primary

MeasureTime frame
Presence or absence of plaque on tooth and implant surfaces (mesial, distal, buccal and lingual surfaces). Timepoint: 1 and 3 months after the intervention. Method of measurement: Clinical dental examination.;The distance between the gingival margin and the depth of the envelope is in millimeters. Timepoint: 1 and 3 months after the intervention. Method of measurement: Clinical dental examination.;Presence or absence of bleeding after probing. Timepoint: 1 and 3 months after the intervention. Method of measurement: Clinical dental examination.;The distance between the acrylic stent and the depth of the pocket. Timepoint: 1 and 3 months after the intervention. Method of measurement: Clinical dental examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad amin Mesforoush

Tabriz University of Medical Sciences

drm.aminmesforoush@yahoo.com+98 41 3237 3382

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 12, 2026