ACTRN12621000396820
Completed
未知
A randomised controlled trial comparing the efficacy of conventional absorbable sutures and knotless absorbable sutures using a split-mouth design.
igel Tan0 sites70 target enrollmentApril 9, 2021
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- igel Tan
- Enrollment
- 70
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Patients referred for third molar removal from a primary care provider
- •2\.Patients who volunteer participation
- •3\.Patients may be either male or female
- •4\.The patient has been screened by the primary investigator or supervising specialist for suitability to participate in the study
- •5\.Are aged between 18 and 44 years
- •6\.Are able to understand verbal and written instructions.
- •7\.Present with bilateral similarly impacted mandibular third molars as determined using Winter’s (1926\) classification system , requiring surgical removal
- •8\.Are able to tolerate outpatient oral surgery under local anaesthetic and intravenous sedation
- •9\.ASA l or ll
- •10\.The patient has provided informed consent regarding:
Exclusion Criteria
- •1\.American society of anaesthesiologists (ASA) physical classification III or IV
- •2\.Polypharmacy (greater than or equal to 5\) medications
- •4\.Patients contraindicated to undergo surgical third molar removal
- •5\.Patients contraindicated to treatment under monoagent midazolam IV sedation
- •6\.Opioid and illict drug addiction
- •7\.Patients that have allergies or contraindications to the procedural usage of:
- •a.midazolam
- •b.dexamethasone
- •c.parecoxib
- •d.paracetamol
Outcomes
Primary Outcomes
Not specified
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