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Clinical Trials/ACTRN12621000396820
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.

Registry
who.int
Start Date
April 9, 2021
End Date
March 25, 2022
Last Updated
4 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
igel Tan

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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