Adult, non-smoker, healthy subjects
Conditions
Interventions
Intervention: receive topical administration of chlorhexidine digluconate 0.2% (Perio-kin, LaboratoriosKin S.A., Barcelona, Spain)immediately after tooth extraction and 500 mg of mefenamic acid
Contr
Sponsors
Dental Faculty - Department of Periodontology - Universitas Padjadjaran, Indonesia
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (i) patients who undergo tooth extraction of mandibular first molar, (ii) aged 18-40 years with American Society of Anesthesiologists physical status I, (iii) do not have the medical history of being allergic to chlorhexidine and mefenamic acid, (iv) is not consuming any other antibiotic, analgesic or anti-inflammation drug(s) at least 7 days prior to the procedure,(v) lack of infection at the tooth indicated for extraction 3 days prior to the extraction procedure, (vi) absence of any pathology at the areaof the tooth indicated for extraction and neighboring teeth.
Exclusion criteria
Exclusion criteria: (i)medically compromised condition, (ii)being pregnant, (iii)with tooth requires surgical extraction were excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Wound diameter, assessed immediately after extraction and 7 days after procedure, in bucco-lingual and mesio-lingual width | — |
Secondary
| Measure | Time frame |
|---|---|
| Healing, assessed using the standardized index by Landry, Turnbull and Howley (1988). | — |
Countries
Asia(except Japan)
Contacts
Public ContactAmaliya Amaliya
Dental Faculty - Universitas Padjadjaran - Indonesia Periodontology
Outcome results
None listed