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临床试验/ACTRN12621000396820
ACTRN12621000396820已完成未知

A randomised controlled trial comparing the efficacy of conventional absorbable sutures and knotless absorbable sutures using a split-mouth design.

igel Tan0 个研究点目标入组 70 人开始时间: 2021年4月9日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
70

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 44 Years(—)
性别
All

入选标准

  • 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:
  • a.Participation in the study
  • i.The use of knotless sutures in the closure of the surgical wound
  • b.Surgical removal of third molars under local anaesthetic and intravenous sedation

排除标准

  • 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
  • e.ibuprofen
  • f.co-amoxiclav
  • g.cefazolin
  • h.clindamycin
  • i.chlorhexidine
  • 8.The presence of symptomatic pericoronitis.
  • 9.The presence of other pathology in the oral cavity.
  • 10.Patients with poor oral hygiene (plaque >1/3 of tooth surface).
  • 11.Pregnant or lactating women.
  • 12.Male patients who do not agree to facial hair removal.
  • 13.Patients who are unable to give informed consent.
  • 14.Patients who decline participation.
  • 15.Patients who are unable to attend the required follow-up appointments.
  • 16.Patients who are unable to comprehend directions and instructions.
  • 17.Patients unwilling to trim facial hair for the purposes for the measurement of facial swelling

研究者

发起方
igel Tan

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