Health Condition 1: K08- Other disorders of teeth and supporting structures
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1 Participants requiring bilateral extraction of molars or premolars 2 Subjects in Age group between 18 to 55 years 3 Individuals under ASA I category 4 Willing to participate and provide informed consent
Exclusion criteria
Exclusion criteria: 1 Allergy to silver or medications used in study 2 Subjects with Acute oral infections 3 Smokers and alcohol consumers 4 Pregnant or lactating women 5 Systemic conditions affecting healing (eg Diabetes Mellitus) 6 Immunocompromised patients 7 Unwilling to participate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of the study is the incidence of postoperative complications at the extraction site, including bleeding, pain, infection, and delayed wound healing, following dental extraction.Timepoint: The primary outcome will be assessed at baseline (immediately after tooth extraction) and during the postoperative follow-up period on postoperative day 1, postoperative day 3, postoperative day 7, and at 4 weeks after extraction. | — |
Secondary
| Measure | Time frame |
|---|---|
| Total number of rescue analgesics tablets paracetamol 500mg consumed by the participant following study side extraction on post operative days.Timepoint: 1st 3rd and 7th postoperative day | — |
Countries
India
Contacts
Yenepoya Dental College