Condition 1: peri-implant mucositis. Condition 2: crestal bone loss. Post-osseointegration biological failure of dental implant Post-osseointegration biological failure of dental implant
Conditions
Interventions
Intervention 1: Intervention group: a half of mouth is intervention group
Doxycycline polymer with trade name of Atridox was placed in annulus space in the final prosthesis delivery time and before closing abutment screw
the evaluation of probing depth, bleeding on probing and the distance of fixture shoulder and crest of bone was done 3, 6 and 9 months after the delivery of finally prothesis. Intervention 2: Contro
No drug use in Annulous space
the evaluation of probing depth, bleeding on probing and the distance of fixture shoulder and crest of bone was done 3, 6 and 9 months after the delivery of finally prothesis.
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: People with at least 2 implantium implants (Dentium, Seoul, South Korea) The site of implant in the area of first and second premolar
Exclusion criteria
Exclusion criteria: Systemic diseases that influence on bone such as; diabetes, renal diseases and osteoporosis Smoking. Periodontal diseases Attached gingival under 2 mm Poor hygiene
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Bleeding on probing. Timepoint: 3, 6 and 12 months after the delivery of final prosthesis. Method of measurement: periodontal probe.;Probing depth in mesial and distal of implant. Timepoint: 3, 6 and 12 months after the delivery of final prosthesis. Method of measurement: periodontal prob.;The measurement of fixture shoulder to the bone crest. Timepoint: 3, 6 and 12 months after the delivery of final prosthesis. Method of measurement: periapical radiography. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahnaz
Tehran University of Medical Sciences
Outcome results
None listed