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

Phase 2

• Conditions: peri-implantitis.; Other endosseous dental implant failure; M27.69

• Registration Number: IRCT20210909052418N1
• Lead Sponsor: Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 November 2021

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 32

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

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

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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.